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Erschienen in: Drug Safety 9/2006

01.09.2006 | Leading Article

Therapeutic Drug Monitoring and Pharmacogenetic Tests as Tools in Pharmacovigilance

verfasst von: Eveline Jaquenoud Sirot, Jan Willem van der Velden, Katharina Rentsch, Chin B. Eap, Pierre Baumann

Erschienen in: Drug Safety | Ausgabe 9/2006

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Abstract

Therapeutic drug monitoring (TDM) and pharmacogenetic tests play a major role in minimising adverse drug reactions and enhancing optimal therapeutic response. The response to medication varies greatly between individuals, according to genetic constitution, age, sex, co-morbidities, environmental factors including diet and lifestyle (e.g. smoking and alcohol intake), and drug-related factors such as pharmacokinetic or pharmacodynamic drug-drug interactions. Most adverse drug reactions are type A reactions, i.e. plasma-level dependent, and represent one of the major causes of hospitalisation, in some cases leading to death. However, they may be avoidable to some extent if pharmacokinetic and pharmacogenetic factors are taken into consideration.
This article provides a review of the literature and describes how to apply and interpret TDM and certain pharmacogenetic tests and is illustrated by case reports. An algorithm on the use of TDM and pharmacogenetic tests to help characterise adverse drug reactions is also presented. Although, in the scientific community, differences in drug response are increasingly recognised, there is an urgent need to translate this knowledge into clinical recommendations. Databases on drug-drug interactions and the impact of pharmacogenetic polymorphisms and adverse drug reaction information systems will be helpful to guide clinicians in individualised treatment choices.
Literatur
1.
Zurück zum Zitat Alexanderson B, Evans DA, Sjoqvist F. Steady-state plasma levels of nortriptyline in twins: influence of genetic factors and drug therapy. BMJ 1969; 4(686): 764–8PubMedCrossRef Alexanderson B, Evans DA, Sjoqvist F. Steady-state plasma levels of nortriptyline in twins: influence of genetic factors and drug therapy. BMJ 1969; 4(686): 764–8PubMedCrossRef
2.
Zurück zum Zitat Alexanderson B. Prediction of steady-state plasma levels of nortriptyline from single oral dose kinetics: a study in twins. Eur J Clin Pharmacol 1973; 6(1): 44–53PubMedCrossRef Alexanderson B. Prediction of steady-state plasma levels of nortriptyline from single oral dose kinetics: a study in twins. Eur J Clin Pharmacol 1973; 6(1): 44–53PubMedCrossRef
3.
Zurück zum Zitat Mahgoub A, Idle JR, Dring LG, et al. Polymorphic hydroxylation of debrisoquine in man. Lancet 1977; II(8038): 584–6CrossRef Mahgoub A, Idle JR, Dring LG, et al. Polymorphic hydroxylation of debrisoquine in man. Lancet 1977; II(8038): 584–6CrossRef
4.
Zurück zum Zitat Bertilsson L, Mellstrom B, Sjoqvist F, et al. Slow hydroxylation of nortriptyline and concomitant poor debrisoquine hydroxylation: clinical implications. Lancet 1981; I(8219): 560–1CrossRef Bertilsson L, Mellstrom B, Sjoqvist F, et al. Slow hydroxylation of nortriptyline and concomitant poor debrisoquine hydroxylation: clinical implications. Lancet 1981; I(8219): 560–1CrossRef
5.
Zurück zum Zitat Ingelman-Sundberg M. Pharmacogenetics: an opportunity for a safer and more efficient pharmacotherapy. J Intern Med 2001; 250(3): 186–200PubMedCrossRef Ingelman-Sundberg M. Pharmacogenetics: an opportunity for a safer and more efficient pharmacotherapy. J Intern Med 2001; 250(3): 186–200PubMedCrossRef
6.
7.
Zurück zum Zitat Wilkinson GR. Drug metabolism and variability among patients in drug response. N Engl J Med 2005; 352(21): 2211–21PubMedCrossRef Wilkinson GR. Drug metabolism and variability among patients in drug response. N Engl J Med 2005; 352(21): 2211–21PubMedCrossRef
8.
Zurück zum Zitat Classen DC, Pestotnik SL, Evans RS, et al. Computerized surveillance of adverse drug events in hospital patients. JAMA 1991; 266(20): 2847–51PubMedCrossRef Classen DC, Pestotnik SL, Evans RS, et al. Computerized surveillance of adverse drug events in hospital patients. JAMA 1991; 266(20): 2847–51PubMedCrossRef
9.
Zurück zum Zitat von Euler M, Eliasson E, Ohlen G, et al. Adverse drug reactions causing hospitalization can be monitored from computerized medical records and thereby indicate the quality of drug utilization. Pharmacoepidemiol Drug Saf 2006; 15(3): 179–84CrossRef von Euler M, Eliasson E, Ohlen G, et al. Adverse drug reactions causing hospitalization can be monitored from computerized medical records and thereby indicate the quality of drug utilization. Pharmacoepidemiol Drug Saf 2006; 15(3): 179–84CrossRef
10.
Zurück zum Zitat Green CF, Mottram DR, Rowe PH, et al. Adverse drug reactions as a cause of admission to an acute medical assessment unit: a pilot study. J Clin Pharm Ther 2000; 25(5): 355–61PubMedCrossRef Green CF, Mottram DR, Rowe PH, et al. Adverse drug reactions as a cause of admission to an acute medical assessment unit: a pilot study. J Clin Pharm Ther 2000; 25(5): 355–61PubMedCrossRef
11.
Zurück zum Zitat Lapeyre-Mestre M, Gary J, Machelard-Roumagnac M, et al. Incidence and cost of adverse drug reactions in a French cancer institute. Eur J Clin Pharmacol 1997; 53(1): 19–22PubMedCrossRef Lapeyre-Mestre M, Gary J, Machelard-Roumagnac M, et al. Incidence and cost of adverse drug reactions in a French cancer institute. Eur J Clin Pharmacol 1997; 53(1): 19–22PubMedCrossRef
12.
Zurück zum Zitat Lazarou J, Pomeranz BH, Corey PN. Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA 1998; 279(15): 1200–5PubMedCrossRef Lazarou J, Pomeranz BH, Corey PN. Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA 1998; 279(15): 1200–5PubMedCrossRef
13.
Zurück zum Zitat Pirmohamed M, James S, Meakin S, et al. Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ 2004; 329(7456): 15–9PubMedCrossRef Pirmohamed M, James S, Meakin S, et al. Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ 2004; 329(7456): 15–9PubMedCrossRef
14.
Zurück zum Zitat Dormann H, Criegee-Rieck M, Neubert A, et al. Lack of awareness of community-acquired adverse drug reactions upon hospital admission: dimensions and consequences of a dilemma. Drug Saf 2003; 26(5): 353–62PubMedCrossRef Dormann H, Criegee-Rieck M, Neubert A, et al. Lack of awareness of community-acquired adverse drug reactions upon hospital admission: dimensions and consequences of a dilemma. Drug Saf 2003; 26(5): 353–62PubMedCrossRef
15.
Zurück zum Zitat Queneau P, Bannwarth B, Carpentier F, et al. Adverse drug effects observed at French admissions departments and emergency services (Prospective study of the National Educational Association for Teaching Therapeutics and proposals for preventive measures [in French]. Bull Acad Natl Med 2003; 187(4): 647–66PubMed Queneau P, Bannwarth B, Carpentier F, et al. Adverse drug effects observed at French admissions departments and emergency services (Prospective study of the National Educational Association for Teaching Therapeutics and proposals for preventive measures [in French]. Bull Acad Natl Med 2003; 187(4): 647–66PubMed
16.
Zurück zum Zitat Johnson JA, Bootman JL. Drug-related morbidity and mortality: a cost-of-illness model. Arch Intern Med 1995; 155(18): 1949–56PubMedCrossRef Johnson JA, Bootman JL. Drug-related morbidity and mortality: a cost-of-illness model. Arch Intern Med 1995; 155(18): 1949–56PubMedCrossRef
17.
Zurück zum Zitat Lepori V, Perren A, Marone C. Adverse internal medicine drug effects at hospital admission [in German]. Schweiz Med Wochenschr 1999; 129(24): 915–22PubMed Lepori V, Perren A, Marone C. Adverse internal medicine drug effects at hospital admission [in German]. Schweiz Med Wochenschr 1999; 129(24): 915–22PubMed
18.
Zurück zum Zitat Schneeweiss S, Hasford J, Gottler M, et al. Admissions caused by adverse drug events to internal medicine and emergency departments in hospitals: a longitudinal population-based study. Eur J Clin Pharmacol 2002; 58(4): 285–91PubMedCrossRef Schneeweiss S, Hasford J, Gottler M, et al. Admissions caused by adverse drug events to internal medicine and emergency departments in hospitals: a longitudinal population-based study. Eur J Clin Pharmacol 2002; 58(4): 285–91PubMedCrossRef
19.
Zurück zum Zitat McDonnell PJ, Jacobs MR. Hospital admissions resulting from preventable adverse drug reactions. Ann Pharmacother 2002; 36(9): 1331–6PubMedCrossRef McDonnell PJ, Jacobs MR. Hospital admissions resulting from preventable adverse drug reactions. Ann Pharmacother 2002; 36(9): 1331–6PubMedCrossRef
20.
Zurück zum Zitat Classen DC, Pestotnik SL, Evans RS, et al. Adverse drug events in hospitalized patients: excess length of stay, extra costs, and attributable mortality. JAMA 1997; 277(4): 301–6PubMedCrossRef Classen DC, Pestotnik SL, Evans RS, et al. Adverse drug events in hospitalized patients: excess length of stay, extra costs, and attributable mortality. JAMA 1997; 277(4): 301–6PubMedCrossRef
21.
Zurück zum Zitat Bates DW, Spell N, Cullen DJ, et al. The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group. JAMA 1997; 277(4): 307–11PubMedCrossRef Bates DW, Spell N, Cullen DJ, et al. The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group. JAMA 1997; 277(4): 307–11PubMedCrossRef
22.
Zurück zum Zitat Ozdemir V, Shear NH, Kalow W. What will be the role of pharmacogenetics in evaluating drug safety and minimising adverse effects? Drug Saf 2001; 24(2): 75–85PubMedCrossRef Ozdemir V, Shear NH, Kalow W. What will be the role of pharmacogenetics in evaluating drug safety and minimising adverse effects? Drug Saf 2001; 24(2): 75–85PubMedCrossRef
23.
Zurück zum Zitat Phillips KA, Veenstra DL, Oren E, et al. Potential role of pharmacogenomics in reducing adverse drug reactions: a systematic review. JAMA 2001; 286(18): 2270–9PubMedCrossRef Phillips KA, Veenstra DL, Oren E, et al. Potential role of pharmacogenomics in reducing adverse drug reactions: a systematic review. JAMA 2001; 286(18): 2270–9PubMedCrossRef
24.
Zurück zum Zitat Guidance for Industry Pharmacogenomic Data Submissions [online]. Available from URL: http://www.fda.gov/cder/guidance/6400fnl.htm [Accessed 2006 Aug 9] Guidance for Industry Pharmacogenomic Data Submissions [online]. Available from URL: http://​www.​fda.​gov/​cder/​guidance/​6400fnl.​htm [Accessed 2006 Aug 9]
25.
Zurück zum Zitat Mancama D, Arranz MJ, Kerwin RW. Genetic predictors of therapeutic response to clozapine: current status of research. CNS Drugs 2002; 16(5): 317–24PubMedCrossRef Mancama D, Arranz MJ, Kerwin RW. Genetic predictors of therapeutic response to clozapine: current status of research. CNS Drugs 2002; 16(5): 317–24PubMedCrossRef
26.
Zurück zum Zitat Van der Weide J, Steijns LS, van Weelden MJ. The effect of smoking and cytochrome P450 CYP1A2 genetic polymorphism on clozapine clearance and dose requirement. Pharmacogenetics 2003; 13(3): 169–72PubMedCrossRef Van der Weide J, Steijns LS, van Weelden MJ. The effect of smoking and cytochrome P450 CYP1A2 genetic polymorphism on clozapine clearance and dose requirement. Pharmacogenetics 2003; 13(3): 169–72PubMedCrossRef
27.
Zurück zum Zitat Eap CB, Bender S, Sirot EJ, et al. Nonresponse to clozapine and ultra-rapid CYP1A2 activity: clinical data and analysis of CYP1A2 gene. J Clin Psychopharmacol 2004; 24(2): 214–9PubMedCrossRef Eap CB, Bender S, Sirot EJ, et al. Nonresponse to clozapine and ultra-rapid CYP1A2 activity: clinical data and analysis of CYP1A2 gene. J Clin Psychopharmacol 2004; 24(2): 214–9PubMedCrossRef
28.
Zurück zum Zitat Mancama D, Kerwin RW. Role of pharmacogenomics in individualising treatment with SSRIs. CNS Drugs 2003; 17(3): 143–51PubMedCrossRef Mancama D, Kerwin RW. Role of pharmacogenomics in individualising treatment with SSRIs. CNS Drugs 2003; 17(3): 143–51PubMedCrossRef
29.
Zurück zum Zitat Lerer B, Macciardi F. Pharmacogenetics of antidepressant and mood-stabilizing drugs: a review of candidate-gene studies and future research directions. Int J Neuropsychopharmacol 2002; 5(3): 255–75PubMedCrossRef Lerer B, Macciardi F. Pharmacogenetics of antidepressant and mood-stabilizing drugs: a review of candidate-gene studies and future research directions. Int J Neuropsychopharmacol 2002; 5(3): 255–75PubMedCrossRef
30.
Zurück zum Zitat Kirchheiner J, Brosen K, Dahl ML, et al. CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: a first step towards subpopulation-specific dosages. Acta Psychiatr Scand 2001; 104(3): 173–92PubMedCrossRef Kirchheiner J, Brosen K, Dahl ML, et al. CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: a first step towards subpopulation-specific dosages. Acta Psychiatr Scand 2001; 104(3): 173–92PubMedCrossRef
31.
Zurück zum Zitat Kirchheiner J, Nickchen K, Bauer M, et al. Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response. Mol Psychiatry 2004; 9(5): 442–73PubMedCrossRef Kirchheiner J, Nickchen K, Bauer M, et al. Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response. Mol Psychiatry 2004; 9(5): 442–73PubMedCrossRef
32.
Zurück zum Zitat Campbell TJ, Williams KM. Therapeutic drug monitoring: antiarrhythmic drugs. Br J Clin Pharmacol 2001; 52Suppl. 1: 21S–34SPubMedCrossRef Campbell TJ, Williams KM. Therapeutic drug monitoring: antiarrhythmic drugs. Br J Clin Pharmacol 2001; 52Suppl. 1: 21S–34SPubMedCrossRef
33.
Zurück zum Zitat Girard T. Pharmakogenetik in der Anasthesie. Schweiz Med Forum 2004; 4: 1199–202 Girard T. Pharmakogenetik in der Anasthesie. Schweiz Med Forum 2004; 4: 1199–202
34.
Zurück zum Zitat Lennard L. Therapeutic drug monitoring of antimetabolic cytotoxic drugs. Br J Clin Pharmacol 1999; 47(2): 131–43PubMedCrossRef Lennard L. Therapeutic drug monitoring of antimetabolic cytotoxic drugs. Br J Clin Pharmacol 1999; 47(2): 131–43PubMedCrossRef
35.
Zurück zum Zitat Lennard L. Therapeutic drug monitoring of cytotoxic drugs. Br J Clin Pharmacol 2001; 52Suppl. 1: 75S–87SPubMedCrossRef Lennard L. Therapeutic drug monitoring of cytotoxic drugs. Br J Clin Pharmacol 2001; 52Suppl. 1: 75S–87SPubMedCrossRef
36.
Zurück zum Zitat Raetz Bravo AE, Tchambaz L, Kraehenbuehl-Melcher A, et al. Prevalence of potentially severe drug-drug interactions in ambulatory patients with dyslipidaemia receiving HMG-CoA reductase inhibitor therapy. Drug Saf 2005; 28(3): 263–75CrossRef Raetz Bravo AE, Tchambaz L, Kraehenbuehl-Melcher A, et al. Prevalence of potentially severe drug-drug interactions in ambulatory patients with dyslipidaemia receiving HMG-CoA reductase inhibitor therapy. Drug Saf 2005; 28(3): 263–75CrossRef
37.
Zurück zum Zitat Starling RC, Hare JM, Hauptman P, et al. Therapeutic drug monitoring for everolismus in heart transplant recipients based on exposure-effect modeling. Am J Transplant 2004; 4(12): 2126–31PubMedCrossRef Starling RC, Hare JM, Hauptman P, et al. Therapeutic drug monitoring for everolismus in heart transplant recipients based on exposure-effect modeling. Am J Transplant 2004; 4(12): 2126–31PubMedCrossRef
38.
Zurück zum Zitat Min DI, Perry PJ, Chen HY, et al. Cyclosporine trough concentrations in predicting allograft rejection and renal toxicity up to 12 months after renal transplantation. Pharmacotherapy 1998; 18(2): 282–7PubMed Min DI, Perry PJ, Chen HY, et al. Cyclosporine trough concentrations in predicting allograft rejection and renal toxicity up to 12 months after renal transplantation. Pharmacotherapy 1998; 18(2): 282–7PubMed
39.
Zurück zum Zitat Eadie MJ. The role of therapeutic drug monitoring in improving the cost effectiveness of anticonvulsant therapy. Clin Pharmacokinet 1995; 29(1): 29–35PubMedCrossRef Eadie MJ. The role of therapeutic drug monitoring in improving the cost effectiveness of anticonvulsant therapy. Clin Pharmacokinet 1995; 29(1): 29–35PubMedCrossRef
40.
Zurück zum Zitat Edwards IR, Aronson JK. Adverse drug reactions: definitions, diagnosis, and management. Lancet 2000; 356(9237): 1255–9PubMedCrossRef Edwards IR, Aronson JK. Adverse drug reactions: definitions, diagnosis, and management. Lancet 2000; 356(9237): 1255–9PubMedCrossRef
41.
Zurück zum Zitat Brown CS, Farmer RG, Soberman JE, et al. Pharmacokinetic factors in the adverse cardiovascular effects of antipsychotic drugs. Clin Pharmacokinet 2004; 43(1): 33–56PubMedCrossRef Brown CS, Farmer RG, Soberman JE, et al. Pharmacokinetic factors in the adverse cardiovascular effects of antipsychotic drugs. Clin Pharmacokinet 2004; 43(1): 33–56PubMedCrossRef
42.
Zurück zum Zitat Mjorndal T, Boman MD, Hagg S, et al. Adverse drug reactions as a cause for admissions to a department of internal medicine. Pharmacoepidemiol Drug Saf 2002; 11(1): 65–72PubMedCrossRef Mjorndal T, Boman MD, Hagg S, et al. Adverse drug reactions as a cause for admissions to a department of internal medicine. Pharmacoepidemiol Drug Saf 2002; 11(1): 65–72PubMedCrossRef
43.
Zurück zum Zitat Jaquenoud Sirot E, Eap CB, Baumann P. Bedeutung von TDM und Pharmakogenetik bei Untersuchungen über Arzneimittelsicherheit in der Psychiatrie. Psychopharmakotherapie 2003; 10(1): 5–10 Jaquenoud Sirot E, Eap CB, Baumann P. Bedeutung von TDM und Pharmakogenetik bei Untersuchungen über Arzneimittelsicherheit in der Psychiatrie. Psychopharmakotherapie 2003; 10(1): 5–10
44.
Zurück zum Zitat Jaquenoud Sirot E, Zullino D. Guide to combination therapy in psychiatry with special emphasis on fluvoxamine. Hannover: Hannoversche Arzte-Verlags-Union, Hannover, 2000 Jaquenoud Sirot E, Zullino D. Guide to combination therapy in psychiatry with special emphasis on fluvoxamine. Hannover: Hannoversche Arzte-Verlags-Union, Hannover, 2000
45.
Zurück zum Zitat Poolsup N, Li Wan PA, Knight TL. Pharmacogenetics and psychopharmacotherapy. J Clin Pharm Ther 2000; 25(3): 197–220PubMedCrossRef Poolsup N, Li Wan PA, Knight TL. Pharmacogenetics and psychopharmacotherapy. J Clin Pharm Ther 2000; 25(3): 197–220PubMedCrossRef
46.
Zurück zum Zitat Ng CH, Schweitzer I, Norman T, et al. The emerging role of pharmacogenetics: implications for clinical psychiatry. Aust N Z J Psychiatry 2004; 38(7): 483–9PubMedCrossRef Ng CH, Schweitzer I, Norman T, et al. The emerging role of pharmacogenetics: implications for clinical psychiatry. Aust N Z J Psychiatry 2004; 38(7): 483–9PubMedCrossRef
47.
Zurück zum Zitat Coutts RT, Urichuk LJ. Polymorphic cytochromes P450 and drugs used in psychiatry. Cell Mol Neurobiol 1999; 19(3): 325–54PubMedCrossRef Coutts RT, Urichuk LJ. Polymorphic cytochromes P450 and drugs used in psychiatry. Cell Mol Neurobiol 1999; 19(3): 325–54PubMedCrossRef
48.
Zurück zum Zitat Murray M. P450 enzymes: inhibition mechanisms, genetic regulation and effects of liver disease. Clin Pharmacokinet 1992; 23(2): 132–46PubMedCrossRef Murray M. P450 enzymes: inhibition mechanisms, genetic regulation and effects of liver disease. Clin Pharmacokinet 1992; 23(2): 132–46PubMedCrossRef
49.
Zurück zum Zitat Guengerich FP, Wu ZL, Bartleson CJ. Function of human cytochrome P450s: characterization of the orphans. Biochem Biophys Res Commun 2005; 338(1): 465–9PubMedCrossRef Guengerich FP, Wu ZL, Bartleson CJ. Function of human cytochrome P450s: characterization of the orphans. Biochem Biophys Res Commun 2005; 338(1): 465–9PubMedCrossRef
50.
Zurück zum Zitat Guengerich FP. Role of cytochrome P450 enzymes in drug-drug interactions. Adv Pharmacol 1997; 43: 7–35PubMedCrossRef Guengerich FP. Role of cytochrome P450 enzymes in drug-drug interactions. Adv Pharmacol 1997; 43: 7–35PubMedCrossRef
51.
Zurück zum Zitat Rotger M, Colombo S, Furrer H, et al. Influence of CYP2B6 polymorphism on plasma and intracellular concentrations and toxicity of efavirenz and nevirapine in HIV-infected patients. Pharmacogenet Genomics 2005; 15(1): 1–5PubMedCrossRef Rotger M, Colombo S, Furrer H, et al. Influence of CYP2B6 polymorphism on plasma and intracellular concentrations and toxicity of efavirenz and nevirapine in HIV-infected patients. Pharmacogenet Genomics 2005; 15(1): 1–5PubMedCrossRef
52.
Zurück zum Zitat Crettol S, Deglon JJ, Besson J, et al. Methadone enantiomer plasma levels, CYP2B6, CYP2C19, and CYP2C9 genotypes, and response to treatment. Clin Pharmacol Ther 2005; 78(6): 593–604PubMedCrossRef Crettol S, Deglon JJ, Besson J, et al. Methadone enantiomer plasma levels, CYP2B6, CYP2C19, and CYP2C9 genotypes, and response to treatment. Clin Pharmacol Ther 2005; 78(6): 593–604PubMedCrossRef
53.
Zurück zum Zitat Hesse LM, Venkatakrishnan K, Court MH, et al. CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants. Drug Metab Dispos 2000; 28(10): 1176–83PubMed Hesse LM, Venkatakrishnan K, Court MH, et al. CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants. Drug Metab Dispos 2000; 28(10): 1176–83PubMed
54.
Zurück zum Zitat Roh HK, Chung JY, Oh DY, et al. Plasma concentrations of haloperidol are related to CYP2D6 genotype at low, but not high doses of haloperidol in Korean schizophrenic patients. Br J Clin Pharmacol 2001; 52(3): 265–71PubMedCrossRef Roh HK, Chung JY, Oh DY, et al. Plasma concentrations of haloperidol are related to CYP2D6 genotype at low, but not high doses of haloperidol in Korean schizophrenic patients. Br J Clin Pharmacol 2001; 52(3): 265–71PubMedCrossRef
55.
Zurück zum Zitat Baumann P, Zullino DF, Eap CB. Enantiomers’ potential in psychopharmacology: a critical analysis with special emphasis on the antidepressant escitalopram. Eur Neuropsychopharmacol 2002; 12(5): 433–44PubMedCrossRef Baumann P, Zullino DF, Eap CB. Enantiomers’ potential in psychopharmacology: a critical analysis with special emphasis on the antidepressant escitalopram. Eur Neuropsychopharmacol 2002; 12(5): 433–44PubMedCrossRef
56.
Zurück zum Zitat Evans WE, Relling MV. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 1999; 286(5439): 487–91PubMedCrossRef Evans WE, Relling MV. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 1999; 286(5439): 487–91PubMedCrossRef
57.
Zurück zum Zitat Vogel F. Moderne probleme der humangenetik. Ergebn Inn Med Kinderheilk 1959; 12: 52–125CrossRef Vogel F. Moderne probleme der humangenetik. Ergebn Inn Med Kinderheilk 1959; 12: 52–125CrossRef
58.
Zurück zum Zitat Pirmohamed M, Park BK. Genetic susceptibility to adverse drug reactions. Trends Pharmacol Sci 2001; 22 (6): 298–305CrossRef Pirmohamed M, Park BK. Genetic susceptibility to adverse drug reactions. Trends Pharmacol Sci 2001; 22 (6): 298–305CrossRef
59.
Zurück zum Zitat Sutrop M. Pharmacogenetics: ethical issues. Bioethics 2004; 18 (4): iii–viiiCrossRef Sutrop M. Pharmacogenetics: ethical issues. Bioethics 2004; 18 (4): iii–viiiCrossRef
60.
Zurück zum Zitat Weber WW. Pharmacogenetics. 1st ed. New York: Oxford University Press, 1997 Weber WW. Pharmacogenetics. 1st ed. New York: Oxford University Press, 1997
61.
Zurück zum Zitat Bertilsson L, Aberg-Wistedt A, Gustafsson LL, et al. Extremely rapid hydroxylation of debrisoquine: a case report with implication for treatment with nortriptyline and other tricyclic antidepressants. Ther Drug Monit 1985; 7(4): 478–80PubMedCrossRef Bertilsson L, Aberg-Wistedt A, Gustafsson LL, et al. Extremely rapid hydroxylation of debrisoquine: a case report with implication for treatment with nortriptyline and other tricyclic antidepressants. Ther Drug Monit 1985; 7(4): 478–80PubMedCrossRef
62.
63.
Zurück zum Zitat Meisel C, Gerloff T, Kirchheiner J, et al. Implications of pharmacogenetics for individualizing drug treatment and for study design. J Mol Med 2003; 81(3): 154–67PubMed Meisel C, Gerloff T, Kirchheiner J, et al. Implications of pharmacogenetics for individualizing drug treatment and for study design. J Mol Med 2003; 81(3): 154–67PubMed
64.
Zurück zum Zitat Lerer B. Pharmacogenetics of psychotropic drugs. New York: Cambridge University Press, 2002CrossRef Lerer B. Pharmacogenetics of psychotropic drugs. New York: Cambridge University Press, 2002CrossRef
65.
Zurück zum Zitat Lindpainter K. Pharmacogenetics and the future of medical practice. J Mol Med 2003; 81: 141–53 Lindpainter K. Pharmacogenetics and the future of medical practice. J Mol Med 2003; 81: 141–53
66.
Zurück zum Zitat Evans WE, McLeod HL. Pharmacogenomics: drug disposition, drug targets, and side effects. N Engl J Med 2003; 348(6): 538–49PubMedCrossRef Evans WE, McLeod HL. Pharmacogenomics: drug disposition, drug targets, and side effects. N Engl J Med 2003; 348(6): 538–49PubMedCrossRef
67.
Zurück zum Zitat Lundqvist E, Johansson I, Ingelman-Sundberg M. Genetic mechanisms for duplication and multiduplication of the human CYP2D6 gene and methods for detection of duplicated CYP2D6 genes. Gene 1999; 226(2): 327–38PubMedCrossRef Lundqvist E, Johansson I, Ingelman-Sundberg M. Genetic mechanisms for duplication and multiduplication of the human CYP2D6 gene and methods for detection of duplicated CYP2D6 genes. Gene 1999; 226(2): 327–38PubMedCrossRef
68.
Zurück zum Zitat Dalen P, Dahl ML, Ruiz ML, et al. 10-Hydroxylation of nortriptyline in white persons with 0, 1, 2, 3, and 13 functional CYP2D6 genes. Clin Pharmacol Ther 1998; 63(4): 444–52PubMedCrossRef Dalen P, Dahl ML, Ruiz ML, et al. 10-Hydroxylation of nortriptyline in white persons with 0, 1, 2, 3, and 13 functional CYP2D6 genes. Clin Pharmacol Ther 1998; 63(4): 444–52PubMedCrossRef
69.
Zurück zum Zitat Lovlie R, Daly AK, Matre GE, et al. Polymorphisms in CYP2D6 duplication-negative individuals with the ultra-rapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultra-rapid metabolism? Pharmacogenetics 2001; 11(1): 45–55PubMedCrossRef Lovlie R, Daly AK, Matre GE, et al. Polymorphisms in CYP2D6 duplication-negative individuals with the ultra-rapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultra-rapid metabolism? Pharmacogenetics 2001; 11(1): 45–55PubMedCrossRef
70.
Zurück zum Zitat Bergmann TK, Bathum L, Brosen K. Duplication of CYP2D6 predicts high clearance of desipramine but high clearance does not predict duplication of CYP2D6. Eur J Clin Pharmacol 2001; 57 (2): 123–7CrossRef Bergmann TK, Bathum L, Brosen K. Duplication of CYP2D6 predicts high clearance of desipramine but high clearance does not predict duplication of CYP2D6. Eur J Clin Pharmacol 2001; 57 (2): 123–7CrossRef
71.
Zurück zum Zitat Xie HG, Kim RB, Wood AJ, et al. Molecular basis of ethnic differences in drug disposition and response. Annu Rev Pharmacol Toxicol 2001; 41: 815–50PubMedCrossRef Xie HG, Kim RB, Wood AJ, et al. Molecular basis of ethnic differences in drug disposition and response. Annu Rev Pharmacol Toxicol 2001; 41: 815–50PubMedCrossRef
72.
Zurück zum Zitat Pi EH, Simpson GM. Cross-cultural psychopharmacology: a current clinical perspective. Psychiatr Serv 2005; 56(1): 31–3PubMedCrossRef Pi EH, Simpson GM. Cross-cultural psychopharmacology: a current clinical perspective. Psychiatr Serv 2005; 56(1): 31–3PubMedCrossRef
73.
Zurück zum Zitat Burroughs VJ, Maxey RW, Levy RA. Racial and ethnic differences in response to medicines: towards individualized pharmaceutical treatment. J Natl Med Assoc 2002; 94(10 Suppl.): 1–26PubMed Burroughs VJ, Maxey RW, Levy RA. Racial and ethnic differences in response to medicines: towards individualized pharmaceutical treatment. J Natl Med Assoc 2002; 94(10 Suppl.): 1–26PubMed
74.
Zurück zum Zitat Ng CH, Chong SA, Lambert T, et al. An inter-ethnic comparison study of clozapine dosage, clinical response and plasma levels. Int Clin Psychopharmacol 2005; 20(3): 163–8PubMedCrossRef Ng CH, Chong SA, Lambert T, et al. An inter-ethnic comparison study of clozapine dosage, clinical response and plasma levels. Int Clin Psychopharmacol 2005; 20(3): 163–8PubMedCrossRef
75.
Zurück zum Zitat Shimada T, Yamazaki H, Mimura M, et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994; 270(1): 414–23PubMed Shimada T, Yamazaki H, Mimura M, et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994; 270(1): 414–23PubMed
76.
Zurück zum Zitat Linnet K, Olesen OV. Metabolism of clozapine by cDNA-expressed human cytochrome P450 enzymes. Drug Metab Dispos 1997; 25(12): 1379–82PubMed Linnet K, Olesen OV. Metabolism of clozapine by cDNA-expressed human cytochrome P450 enzymes. Drug Metab Dispos 1997; 25(12): 1379–82PubMed
77.
Zurück zum Zitat Goldstein JA, Ishizaki T, Chiba K, et al. Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations. Pharmacogenetics 1997; 7(1): 59–64PubMedCrossRef Goldstein JA, Ishizaki T, Chiba K, et al. Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations. Pharmacogenetics 1997; 7(1): 59–64PubMedCrossRef
78.
Zurück zum Zitat Matsuda KT, Cho MC, Lin KM, et al. Clozapine dosage, serum levels, efficacy, and side-effect profiles: a comparison of Korean-American and Caucasian patients. Psychopharmacol Bull 1996; 32: 253–7PubMed Matsuda KT, Cho MC, Lin KM, et al. Clozapine dosage, serum levels, efficacy, and side-effect profiles: a comparison of Korean-American and Caucasian patients. Psychopharmacol Bull 1996; 32: 253–7PubMed
79.
Zurück zum Zitat Nakajima M, Yokoi T, Mizutani M, et al. Genetic polymorphism in the 5′-flanking region of human CYP1A2 gene: effect on the CYP1A2 inducibility in humans. J Biochem (Tokyo) 1999; 125(4): 803–8CrossRef Nakajima M, Yokoi T, Mizutani M, et al. Genetic polymorphism in the 5′-flanking region of human CYP1A2 gene: effect on the CYP1A2 inducibility in humans. J Biochem (Tokyo) 1999; 125(4): 803–8CrossRef
80.
Zurück zum Zitat Allorge D, Chevalier D, Lo-Guidice JM, et al. Identification of a novel splice-site mutation in the CYP1A2 gene. Br J Clin Pharmacol 2003; 56(3): 341–4PubMedCrossRef Allorge D, Chevalier D, Lo-Guidice JM, et al. Identification of a novel splice-site mutation in the CYP1A2 gene. Br J Clin Pharmacol 2003; 56(3): 341–4PubMedCrossRef
81.
Zurück zum Zitat Aklillu E, Carrillo JA, Makonnen E, et al. Genetic polymorphism of CYP1A2 in Ethiopians affecting induction and expression: characterization of novel haplotypes with singlenucleotide polymorphisms in intron 1. Mol Pharmacol 2003; 64(3): 659–69PubMedCrossRef Aklillu E, Carrillo JA, Makonnen E, et al. Genetic polymorphism of CYP1A2 in Ethiopians affecting induction and expression: characterization of novel haplotypes with singlenucleotide polymorphisms in intron 1. Mol Pharmacol 2003; 64(3): 659–69PubMedCrossRef
82.
Zurück zum Zitat Sachse C, Brockmöller J, Bauer S, et al. Functional significance of a C → A polymorphism in intron 1 of the cytochrome P450 CYP1A2 gene tested with caffeine. Br J Clin Pharmacol 1999; 47(4): 445–9PubMedCrossRef Sachse C, Brockmöller J, Bauer S, et al. Functional significance of a C → A polymorphism in intron 1 of the cytochrome P450 CYP1A2 gene tested with caffeine. Br J Clin Pharmacol 1999; 47(4): 445–9PubMedCrossRef
83.
Zurück zum Zitat Han XM, Ou-Yang DS, Lu PX, et al. Plasma caffeine metabolite ratio (17X/137X) in vivo associated with G-2964A and C734A polymorphisms of human CYP1A2. Pharmacogenetics 2001; 11(5): 429–35PubMedCrossRef Han XM, Ou-Yang DS, Lu PX, et al. Plasma caffeine metabolite ratio (17X/137X) in vivo associated with G-2964A and C734A polymorphisms of human CYP1A2. Pharmacogenetics 2001; 11(5): 429–35PubMedCrossRef
84.
Zurück zum Zitat Aynacioglu AS, Brockmöller J, Bauer S, et al. Frequency of cytochrome P450 CYP2C9 variants in a Turkish population and functional relevance for phenytoin. Br J Clin Pharmacol 1999; 48(3): 409–15PubMedCrossRef Aynacioglu AS, Brockmöller J, Bauer S, et al. Frequency of cytochrome P450 CYP2C9 variants in a Turkish population and functional relevance for phenytoin. Br J Clin Pharmacol 1999; 48(3): 409–15PubMedCrossRef
85.
Zurück zum Zitat Garcia-Martin E, Martinez C, Ladero JM, et al. High frequency of mutations related to impaired CYP2C9 metabolism in a Caucasian population. Eur J Clin Pharmacol 2001; 57(1): 47–9PubMedCrossRef Garcia-Martin E, Martinez C, Ladero JM, et al. High frequency of mutations related to impaired CYP2C9 metabolism in a Caucasian population. Eur J Clin Pharmacol 2001; 57(1): 47–9PubMedCrossRef
86.
Zurück zum Zitat Scordo MG, Caputi AP, D’Arrigo C, et al. Allele and genotype frequencies of CYP2C9, CYP2C19 and CYP2D6 in an Italian population. Pharmacol Res 2004; 50(2): 195–200PubMedCrossRef Scordo MG, Caputi AP, D’Arrigo C, et al. Allele and genotype frequencies of CYP2C9, CYP2C19 and CYP2D6 in an Italian population. Pharmacol Res 2004; 50(2): 195–200PubMedCrossRef
87.
Zurück zum Zitat Wang SL, Huang J, Lai MD, et al. Detection of CYP2C9 polymorphism based on the polymerase chain reaction in Chinese. Pharmacogenetics 1995; 5(1): 37–42PubMedCrossRef Wang SL, Huang J, Lai MD, et al. Detection of CYP2C9 polymorphism based on the polymerase chain reaction in Chinese. Pharmacogenetics 1995; 5(1): 37–42PubMedCrossRef
88.
Zurück zum Zitat Kimura M, Ieiri I, Mamiya K, et al. Genetic polymorphism of cytochrome P450s, CYP2C19, and CYP2C9 in a Japanese population. Ther Drug Monit 1998; 20(3): 243–7PubMedCrossRef Kimura M, Ieiri I, Mamiya K, et al. Genetic polymorphism of cytochrome P450s, CYP2C19, and CYP2C9 in a Japanese population. Ther Drug Monit 1998; 20(3): 243–7PubMedCrossRef
89.
Zurück zum Zitat Scordo MG, Aklillu E, Yasar U, et al. Genetic polymorphism of cytochrome P4502C9 in a Caucasian and a black African population. Br J Clin Pharmacol 2001; 52(4): 447–50PubMedCrossRef Scordo MG, Aklillu E, Yasar U, et al. Genetic polymorphism of cytochrome P4502C9 in a Caucasian and a black African population. Br J Clin Pharmacol 2001; 52(4): 447–50PubMedCrossRef
90.
Zurück zum Zitat Gaedigk A. Interethnic differences of drug-metabolizing enzymes. Int J Clin Pharmacol Ther 2000; 38(2): 61–8PubMed Gaedigk A. Interethnic differences of drug-metabolizing enzymes. Int J Clin Pharmacol Ther 2000; 38(2): 61–8PubMed
91.
Zurück zum Zitat Dandara C, Masimirembwa CM, Magimba A, et al. Genetic polymorphism of CYP2D6 and CYP2C19 in east- and southern African populations including psychiatric patients. Eur J Clin Pharmacol 2001; 57(1): 11–7PubMedCrossRef Dandara C, Masimirembwa CM, Magimba A, et al. Genetic polymorphism of CYP2D6 and CYP2C19 in east- and southern African populations including psychiatric patients. Eur J Clin Pharmacol 2001; 57(1): 11–7PubMedCrossRef
92.
Zurück zum Zitat Evans DA, Krahn P, Narayanan N. The mephenytoin (cytochrome P4502C19). and dextromethorphan (cytochrome P4502D6). polymorphisms in Saudi Arabians and Filipinos. Pharmacogenetics 1995; 5(2): 64–71PubMedCrossRef Evans DA, Krahn P, Narayanan N. The mephenytoin (cytochrome P4502C19). and dextromethorphan (cytochrome P4502D6). polymorphisms in Saudi Arabians and Filipinos. Pharmacogenetics 1995; 5(2): 64–71PubMedCrossRef
93.
Zurück zum Zitat Aynacioglu AS, Sachse C, Bozkurt A, et al. Low frequency of defective alleles of cytochrome P450 enzymes 2C19 and 2D6 in the Turkish population. Clin Pharmacol Ther 1999; 66(2): 185–92PubMed Aynacioglu AS, Sachse C, Bozkurt A, et al. Low frequency of defective alleles of cytochrome P450 enzymes 2C19 and 2D6 in the Turkish population. Clin Pharmacol Ther 1999; 66(2): 185–92PubMed
94.
Zurück zum Zitat Roh HK, Dahl ML, Johansson I, et al. Debrisoquine and Smephenytoin hydroxylation phenotypes and genotypes in a Korean population. Pharmacogenetics 1996; 6(5): 441–7PubMedCrossRef Roh HK, Dahl ML, Johansson I, et al. Debrisoquine and Smephenytoin hydroxylation phenotypes and genotypes in a Korean population. Pharmacogenetics 1996; 6(5): 441–7PubMedCrossRef
95.
Zurück zum Zitat Roh HK, Dahl ML, Tybring G, et al. CYP2C19 genotype and phenotype determined by omeprazole in a Korean population. Pharmacogenetics 1996; 6(6): 547–51PubMedCrossRef Roh HK, Dahl ML, Tybring G, et al. CYP2C19 genotype and phenotype determined by omeprazole in a Korean population. Pharmacogenetics 1996; 6(6): 547–51PubMedCrossRef
96.
Zurück zum Zitat Itoh K, Inoue K, Yanagiwara S, et al. A rapid and simple detection of genetic defects responsible for the phenotypic polymorphism of cytochrome P4502C19. Biol Pharm Bull 1999; 22(1): 77–9PubMedCrossRef Itoh K, Inoue K, Yanagiwara S, et al. A rapid and simple detection of genetic defects responsible for the phenotypic polymorphism of cytochrome P4502C19. Biol Pharm Bull 1999; 22(1): 77–9PubMedCrossRef
97.
Zurück zum Zitat Kimura M, Ieiri I, Mamiya K, et al. Genetic polymorphism of cytochrome P450s, CYP2C19, and CYP2C9 in a Japanese population. Ther Drug Monit 1998; 20(3): 243–7PubMedCrossRef Kimura M, Ieiri I, Mamiya K, et al. Genetic polymorphism of cytochrome P450s, CYP2C19, and CYP2C9 in a Japanese population. Ther Drug Monit 1998; 20(3): 243–7PubMedCrossRef
98.
Zurück zum Zitat Sachse C, Brockmöller J, Bauer S, et al. Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am J Hum Genet 1997; 60(2): 284–95PubMed Sachse C, Brockmöller J, Bauer S, et al. Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am J Hum Genet 1997; 60(2): 284–95PubMed
99.
Zurück zum Zitat Dahl AA, Lowert A, Asserson S, et al. Hydroxylation polymorphism of debrisoquine hydroxylase (CYP2D6) in patients with schizophrenia in Norway and Denmark. Hum Psychopharmacol Clin Exp 1998; 13: 509–11CrossRef Dahl AA, Lowert A, Asserson S, et al. Hydroxylation polymorphism of debrisoquine hydroxylase (CYP2D6) in patients with schizophrenia in Norway and Denmark. Hum Psychopharmacol Clin Exp 1998; 13: 509–11CrossRef
100.
Zurück zum Zitat Tefre T, Daly AK, Armstrong M, et al. Genotyping of the CYP2D6 gene in Norwegian lung cancer patients and controls. Pharmacogenetics 1994; 4(2): 47–57PubMedCrossRef Tefre T, Daly AK, Armstrong M, et al. Genotyping of the CYP2D6 gene in Norwegian lung cancer patients and controls. Pharmacogenetics 1994; 4(2): 47–57PubMedCrossRef
101.
Zurück zum Zitat Madsen H, Nielsen KK, Brosen K. Imipramine metabolism in relation to the sparteine and mephenytoin oxidation polymorphisms: a population study. Br J Clin Pharmacol 1995; 39(4): 433–9PubMedCrossRef Madsen H, Nielsen KK, Brosen K. Imipramine metabolism in relation to the sparteine and mephenytoin oxidation polymorphisms: a population study. Br J Clin Pharmacol 1995; 39(4): 433–9PubMedCrossRef
102.
Zurück zum Zitat Agundez JA, Ledesma MC, Ladero JM, et al. Prevalence of CYP2D6 gene duplication and its repercussion on the oxidative phenotype in a white population. Clin Pharmacol Ther 1995; 57(3): 265–9PubMedCrossRef Agundez JA, Ledesma MC, Ladero JM, et al. Prevalence of CYP2D6 gene duplication and its repercussion on the oxidative phenotype in a white population. Clin Pharmacol Ther 1995; 57(3): 265–9PubMedCrossRef
103.
Zurück zum Zitat McLellan RA, Oscarson M, Seidegard J, et al. Frequent occurrence of CYP2D6 gene duplication in Saudi Arabians. Pharmacogenetics 1997; 7(3): 187–91PubMedCrossRef McLellan RA, Oscarson M, Seidegard J, et al. Frequent occurrence of CYP2D6 gene duplication in Saudi Arabians. Pharmacogenetics 1997; 7(3): 187–91PubMedCrossRef
104.
Zurück zum Zitat Ji L, Pan S, Wu J, et al. Genetic polymorphisms of CYP2D6 in Chinese mainland. Chin Med J (Engl) 2002; 115(12): 1780–4 Ji L, Pan S, Wu J, et al. Genetic polymorphisms of CYP2D6 in Chinese mainland. Chin Med J (Engl) 2002; 115(12): 1780–4
105.
Zurück zum Zitat Bradford LD, Gaedigk A, Leeder JS. High frequency of CYP2D6 poor and “intermediate” metabolizers in black populations: a review and preliminary data. Psychopharmacol Bull 1998; 34(4): 797–804PubMed Bradford LD, Gaedigk A, Leeder JS. High frequency of CYP2D6 poor and “intermediate” metabolizers in black populations: a review and preliminary data. Psychopharmacol Bull 1998; 34(4): 797–804PubMed
106.
Zurück zum Zitat Bradford LD, Kirlin WG. Polymorphism of CYP2D6 in Black populations: implications for psychopharmacology. Int J Neuropsychopharmcol 1998; 1(2): 173–85CrossRef Bradford LD, Kirlin WG. Polymorphism of CYP2D6 in Black populations: implications for psychopharmacology. Int J Neuropsychopharmcol 1998; 1(2): 173–85CrossRef
107.
Zurück zum Zitat Bradford LD. CYP2D6 allele frequency in European Caucasians, Asians, Africans and their descendants. Pharmacogenomics 2002; 3(2): 229–43PubMedCrossRef Bradford LD. CYP2D6 allele frequency in European Caucasians, Asians, Africans and their descendants. Pharmacogenomics 2002; 3(2): 229–43PubMedCrossRef
108.
Zurück zum Zitat Kuehl P, Zhang J, Lin Y, et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression. Nat Genet 2001; 27(4): 383–91PubMedCrossRef Kuehl P, Zhang J, Lin Y, et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression. Nat Genet 2001; 27(4): 383–91PubMedCrossRef
109.
Zurück zum Zitat Saeki M, Saito Y, Nakamura T, et al. Single nucleotide polymorphisms and haplotype frequencies of CYP3A5 in a Japanese population. Hum Mutat 2003; 21(6): 653PubMedCrossRef Saeki M, Saito Y, Nakamura T, et al. Single nucleotide polymorphisms and haplotype frequencies of CYP3A5 in a Japanese population. Hum Mutat 2003; 21(6): 653PubMedCrossRef
110.
Zurück zum Zitat Chou FC, Tzeng SJ, Huang JD. Genetic polymorphism of cytochrome P450 3A5 in Chinese. Drug Metab Dispos 2001; 29(9): 1205–9PubMed Chou FC, Tzeng SJ, Huang JD. Genetic polymorphism of cytochrome P450 3A5 in Chinese. Drug Metab Dispos 2001; 29(9): 1205–9PubMed
111.
Zurück zum Zitat Dai D, Tang J, Rose R, et al. Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos. J Pharmacol Exp Ther 2001; 299(3): 825–31PubMed Dai D, Tang J, Rose R, et al. Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos. J Pharmacol Exp Ther 2001; 299(3): 825–31PubMed
112.
Zurück zum Zitat Bertilsson L, Lou YQ, Du YL, et al. Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and Smephenytoin. Clin Pharmacol Ther 1992; 51(4): 388–97PubMedCrossRef Bertilsson L, Lou YQ, Du YL, et al. Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and Smephenytoin. Clin Pharmacol Ther 1992; 51(4): 388–97PubMedCrossRef
113.
Zurück zum Zitat Fukuda T, Yamamoto I, Nishida Y, et al. Effect of the CYP2D6*10 genotype on venlafaxine pharmacokinetics in healthy adult volunteers. Br J Clin Pharmacol 1999; 47(4): 450–3PubMedCrossRef Fukuda T, Yamamoto I, Nishida Y, et al. Effect of the CYP2D6*10 genotype on venlafaxine pharmacokinetics in healthy adult volunteers. Br J Clin Pharmacol 1999; 47(4): 450–3PubMedCrossRef
114.
Zurück zum Zitat Bertilsson L, Dahl ML, Dalen P, et al. Molecular genetics of CYP2D6: clinical relevance with focus on psychotropic drugs. Br J Clin Pharmacol 2002; 53(2): 111–22PubMedCrossRef Bertilsson L, Dahl ML, Dalen P, et al. Molecular genetics of CYP2D6: clinical relevance with focus on psychotropic drugs. Br J Clin Pharmacol 2002; 53(2): 111–22PubMedCrossRef
115.
Zurück zum Zitat Bertilsson L, Dahl ML, Tybring G. Pharmacogenetics of antidepressants: clinical aspects. Acta Psychiatr Scand Suppl 1997; 391: 14–21PubMedCrossRef Bertilsson L, Dahl ML, Tybring G. Pharmacogenetics of antidepressants: clinical aspects. Acta Psychiatr Scand Suppl 1997; 391: 14–21PubMedCrossRef
116.
Zurück zum Zitat Kirchheiner J, Bertilsson L, Bruus H, et al. Individualized medicine: implementation of pharmacogenetic diagnostics in antidepressant drug treatment of major depressive disorders. Pharmacopsychiatry 2003; 36Suppl. 3: S235–43PubMed Kirchheiner J, Bertilsson L, Bruus H, et al. Individualized medicine: implementation of pharmacogenetic diagnostics in antidepressant drug treatment of major depressive disorders. Pharmacopsychiatry 2003; 36Suppl. 3: S235–43PubMed
117.
Zurück zum Zitat Kirchheiner J, Fuhr U, Brockmöller J. Pharmacogenetics-based therapeutic recommendations: ready for clinical practice? Nat Rev Drug Discov 2005; 4(8): 639–47PubMedCrossRef Kirchheiner J, Fuhr U, Brockmöller J. Pharmacogenetics-based therapeutic recommendations: ready for clinical practice? Nat Rev Drug Discov 2005; 4(8): 639–47PubMedCrossRef
118.
Zurück zum Zitat Lessard E, Yessine MA, Hamelin BA, et al. Influence of CYP2D6 activity on the disposition and cardiovascular toxicity of the antidepressant agent venlafaxine in humans. Pharmacogenetics 1999; 9(4): 435–43PubMed Lessard E, Yessine MA, Hamelin BA, et al. Influence of CYP2D6 activity on the disposition and cardiovascular toxicity of the antidepressant agent venlafaxine in humans. Pharmacogenetics 1999; 9(4): 435–43PubMed
119.
Zurück zum Zitat Gasche Y, Daali Y, Fathi M, et al. Codeine intoxication associated with ultra-rapid CYP2D6 metabolism. N Engl J Med 2004; 351(27): 2827–31PubMedCrossRef Gasche Y, Daali Y, Fathi M, et al. Codeine intoxication associated with ultra-rapid CYP2D6 metabolism. N Engl J Med 2004; 351(27): 2827–31PubMedCrossRef
120.
Zurück zum Zitat Dalen P, Frengell C, Dahl ML, et al. Quick onset of severe abdominal pain after codeine in an ultra-rapid metabolizer of debrisoquine. Ther Drug Monit 1997; 19(5): 543–4PubMedCrossRef Dalen P, Frengell C, Dahl ML, et al. Quick onset of severe abdominal pain after codeine in an ultra-rapid metabolizer of debrisoquine. Ther Drug Monit 1997; 19(5): 543–4PubMedCrossRef
121.
Zurück zum Zitat Baumann P, Hiemke C, Ulrich S, et al. The AGNP-TDM expert group consensus guidelines: therapeutic drug monitoring in psychiatry. Pharmacopsychiatry 2004; 37(6): 243–65PubMedCrossRef Baumann P, Hiemke C, Ulrich S, et al. The AGNP-TDM expert group consensus guidelines: therapeutic drug monitoring in psychiatry. Pharmacopsychiatry 2004; 37(6): 243–65PubMedCrossRef
122.
Zurück zum Zitat Stephan PL, Jaquenoud Sirot E, Mueller B, et al. Adverse drug reactions following nonresponse in a depressed patient with CYP2D6 deficiency and low CYP 3A4/5 activity: a pharmacovigilance case report. Pharmacopsychiatry 2006; 39(4): 150–2PubMedCrossRef Stephan PL, Jaquenoud Sirot E, Mueller B, et al. Adverse drug reactions following nonresponse in a depressed patient with CYP2D6 deficiency and low CYP 3A4/5 activity: a pharmacovigilance case report. Pharmacopsychiatry 2006; 39(4): 150–2PubMedCrossRef
123.
Zurück zum Zitat Furuta T, Shirai N, Xiao F, et al. Effect of high-dose lansoprazole on intragastic pH in subjects who are homozygous extensive metabolizers of cytochrome P4502C19. Clin Pharmacol Ther 2001; 70(5): 484–92PubMedCrossRef Furuta T, Shirai N, Xiao F, et al. Effect of high-dose lansoprazole on intragastic pH in subjects who are homozygous extensive metabolizers of cytochrome P4502C19. Clin Pharmacol Ther 2001; 70(5): 484–92PubMedCrossRef
124.
Zurück zum Zitat Furuta T, Ohashi K, Kosuge K, et al. CYP2C19 genotype status and effect of omeprazole on intragastric pH in humans. Clin Pharmacol Ther 1999; 65(5): 552–61PubMedCrossRef Furuta T, Ohashi K, Kosuge K, et al. CYP2C19 genotype status and effect of omeprazole on intragastric pH in humans. Clin Pharmacol Ther 1999; 65(5): 552–61PubMedCrossRef
125.
Zurück zum Zitat Furuta T, Takashima M, Shirai N, et al. Cure of refractory duodenal ulcer and infection caused by Helicobacter pylori by high doses of omeprazole and amoxicillin in a homozygous CYP2C19 extensive metabolizer patient. Clin Pharmacol Ther 2000; 67(6): 684–9PubMedCrossRef Furuta T, Takashima M, Shirai N, et al. Cure of refractory duodenal ulcer and infection caused by Helicobacter pylori by high doses of omeprazole and amoxicillin in a homozygous CYP2C19 extensive metabolizer patient. Clin Pharmacol Ther 2000; 67(6): 684–9PubMedCrossRef
126.
Zurück zum Zitat Furuta T, Shirai N, Takashima M, et al. Effect of genotypic differences in CYP2C19 on cure rates for Helicobacter pylori infection by triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin. Clin Pharmacol Ther 2001; 69(3): 158–68PubMedCrossRef Furuta T, Shirai N, Takashima M, et al. Effect of genotypic differences in CYP2C19 on cure rates for Helicobacter pylori infection by triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin. Clin Pharmacol Ther 2001; 69(3): 158–68PubMedCrossRef
127.
Zurück zum Zitat Furuta T, Ohashi K, Kamata T, et al. Effect of genetic differences in omeprazole metabolism on cure rates for Helicobacter pylori infection and peptic ulcer. Ann Intern Med 1998; 129(12): 1027–30PubMed Furuta T, Ohashi K, Kamata T, et al. Effect of genetic differences in omeprazole metabolism on cure rates for Helicobacter pylori infection and peptic ulcer. Ann Intern Med 1998; 129(12): 1027–30PubMed
128.
Zurück zum Zitat Higashi MK, Veenstra DL, Kondo LM, et al. Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy. JAMA 2002; 287(13): 1690–8PubMedCrossRef Higashi MK, Veenstra DL, Kondo LM, et al. Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy. JAMA 2002; 287(13): 1690–8PubMedCrossRef
129.
Zurück zum Zitat Scordo MG, Pengo V, Spina E, et al. Influence of CYP2C9 and CYP2C19 genetic polymorphisms on warfarin maintenance dose and metabolic clearance. Clin Pharmacol Ther 2002; 72(6): 702–10PubMedCrossRef Scordo MG, Pengo V, Spina E, et al. Influence of CYP2C9 and CYP2C19 genetic polymorphisms on warfarin maintenance dose and metabolic clearance. Clin Pharmacol Ther 2002; 72(6): 702–10PubMedCrossRef
130.
Zurück zum Zitat Hillman MA, Wilke RA, Yale SH, et al. A prospective, randomized pilot trial of model-based warfarin dose initiation using CYP2C9 genotype and clinical data. Clin Med Res 2005; 3(3): 137–45PubMedCrossRef Hillman MA, Wilke RA, Yale SH, et al. A prospective, randomized pilot trial of model-based warfarin dose initiation using CYP2C9 genotype and clinical data. Clin Med Res 2005; 3(3): 137–45PubMedCrossRef
131.
Zurück zum Zitat Ozdemir V, Kalow W, Posner P, et al. CYP1A2 activity as measured by a caffeine test predicts clozapine and active metabolite steady-state concentration in patients with schizophrenia. J Clin Psychopharmacol 2001; 21(4): 398–407PubMedCrossRef Ozdemir V, Kalow W, Posner P, et al. CYP1A2 activity as measured by a caffeine test predicts clozapine and active metabolite steady-state concentration in patients with schizophrenia. J Clin Psychopharmacol 2001; 21(4): 398–407PubMedCrossRef
132.
Zurück zum Zitat Eap CB, Buclin T, Hustert E, et al. Pharmacokinetics of midazolam in CYP3A4 and CYP3A5 genotyped subjects. Eur J Clin Pharmacol 2004; 60(4): 231–6PubMed Eap CB, Buclin T, Hustert E, et al. Pharmacokinetics of midazolam in CYP3A4 and CYP3A5 genotyped subjects. Eur J Clin Pharmacol 2004; 60(4): 231–6PubMed
133.
Zurück zum Zitat Shah RR. Pharmacogenetic aspects of drug-induced torsade de pointes: potential tool for improving clinical drug development and prescribing. Drug Saf 2004; 27(3): 145–72PubMedCrossRef Shah RR. Pharmacogenetic aspects of drug-induced torsade de pointes: potential tool for improving clinical drug development and prescribing. Drug Saf 2004; 27(3): 145–72PubMedCrossRef
134.
Zurück zum Zitat Brandolese R, Scordo MG, Spina E, et al. Severe phenytoin intoxication in a subject homozygous for CYP2C9*3. Clin Pharmacol Ther 2001; 70(4): 391–4PubMed Brandolese R, Scordo MG, Spina E, et al. Severe phenytoin intoxication in a subject homozygous for CYP2C9*3. Clin Pharmacol Ther 2001; 70(4): 391–4PubMed
135.
Zurück zum Zitat Kidd RS, Curry TB, Gallagher S, et al. Identification of a null allele of CYP2C9 in an African-American exhibiting toxicity to phenytoin. Pharmacogenetics 2001; 11(9): 803–8PubMedCrossRef Kidd RS, Curry TB, Gallagher S, et al. Identification of a null allele of CYP2C9 in an African-American exhibiting toxicity to phenytoin. Pharmacogenetics 2001; 11(9): 803–8PubMedCrossRef
136.
Zurück zum Zitat Aithal GP, Day CP, Kesteven PJ, et al. Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications. Lancet 1999; 353(9154): 717–9PubMedCrossRef Aithal GP, Day CP, Kesteven PJ, et al. Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications. Lancet 1999; 353(9154): 717–9PubMedCrossRef
137.
Zurück zum Zitat Kidd RS, Straughn AB, Meyer MC, et al. Pharmacokinetics of chlorpheniramine, phenytoin, glipizide and nifedipine in an individual homozygous for the CYP2C9*3 allele. Pharmacogenetics 1999; 9(1): 71–80PubMedCrossRef Kidd RS, Straughn AB, Meyer MC, et al. Pharmacokinetics of chlorpheniramine, phenytoin, glipizide and nifedipine in an individual homozygous for the CYP2C9*3 allele. Pharmacogenetics 1999; 9(1): 71–80PubMedCrossRef
138.
Zurück zum Zitat Miners JO, Birkett DJ. Cytochrome P4502C9: an enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 1998; 45(6): 525–38PubMedCrossRef Miners JO, Birkett DJ. Cytochrome P4502C9: an enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 1998; 45(6): 525–38PubMedCrossRef
139.
Zurück zum Zitat Kapitany T, Meszaros K, Lenzinger E, et al. Genetic polymorphisms for drug metabolism (CYP2D6) and tardive dyskinesia in schizophrenia. Schizophr Res 1998; 32(2): 101–6PubMedCrossRef Kapitany T, Meszaros K, Lenzinger E, et al. Genetic polymorphisms for drug metabolism (CYP2D6) and tardive dyskinesia in schizophrenia. Schizophr Res 1998; 32(2): 101–6PubMedCrossRef
140.
Zurück zum Zitat Brosen K. Drug-metabolizing enzymes and therapeutic drug monitoring in psychiatry. Ther Drug Monit 1996; 18(4): 393–6PubMedCrossRef Brosen K. Drug-metabolizing enzymes and therapeutic drug monitoring in psychiatry. Ther Drug Monit 1996; 18(4): 393–6PubMedCrossRef
141.
Zurück zum Zitat Dahl ML, Sjoqvist F. Pharmacogenetic methods as a complement to therapeutic monitoring of antidepressants and neuroleptics. Ther Drug Monit 2000; 22(1): 114–7PubMedCrossRef Dahl ML, Sjoqvist F. Pharmacogenetic methods as a complement to therapeutic monitoring of antidepressants and neuroleptics. Ther Drug Monit 2000; 22(1): 114–7PubMedCrossRef
142.
Zurück zum Zitat DeVane CL. Pharmacogenetics and drug metabolism of newer antidepressant agents. J Clin Psychiatry 1994; 55Suppl.: 38–45PubMed DeVane CL. Pharmacogenetics and drug metabolism of newer antidepressant agents. J Clin Psychiatry 1994; 55Suppl.: 38–45PubMed
143.
Zurück zum Zitat Otani K, Aoshima T. Pharmacogenetics of classical and new antipsychotic drugs. Ther Drug Monit 2000; 22(1): 118–21PubMedCrossRef Otani K, Aoshima T. Pharmacogenetics of classical and new antipsychotic drugs. Ther Drug Monit 2000; 22(1): 118–21PubMedCrossRef
144.
Zurück zum Zitat Steimer W, Potter JM. Pharmacogenetic screening and therapeutic drugs. Clin Chim Acta 2002; 315(1-2): 137–55PubMedCrossRef Steimer W, Potter JM. Pharmacogenetic screening and therapeutic drugs. Clin Chim Acta 2002; 315(1-2): 137–55PubMedCrossRef
145.
Zurück zum Zitat Wilke RA, Reif DM, Moore JH. Combinatorial pharmacogenetics. Nat Rev Drug Discov 2005; 4(11): 911–8PubMedCrossRef Wilke RA, Reif DM, Moore JH. Combinatorial pharmacogenetics. Nat Rev Drug Discov 2005; 4(11): 911–8PubMedCrossRef
146.
Zurück zum Zitat Lange-Asschenfeldt C, Weigmann H, Hiemke C, et al. Serotonin syndrome as a result of fluoxetine in a patient with tramadol abuse: plasma level-correlated symptomatology. J Clin Psychopharmacol 2002; 22(4): 440–1PubMedCrossRef Lange-Asschenfeldt C, Weigmann H, Hiemke C, et al. Serotonin syndrome as a result of fluoxetine in a patient with tramadol abuse: plasma level-correlated symptomatology. J Clin Psychopharmacol 2002; 22(4): 440–1PubMedCrossRef
147.
Zurück zum Zitat Mahlberg R, Kunz D, Sasse J, et al. Serotonin syndrome with tramadol and citalopram (letter). Am J Psychiatry 2004; 161(6): 1129PubMedCrossRef Mahlberg R, Kunz D, Sasse J, et al. Serotonin syndrome with tramadol and citalopram (letter). Am J Psychiatry 2004; 161(6): 1129PubMedCrossRef
148.
Zurück zum Zitat Kesavan S, Sobala GM. Serotonin syndrome with fluoxetine plus tramadol. J R Soc Med 1999; 92(9): 474–5PubMed Kesavan S, Sobala GM. Serotonin syndrome with fluoxetine plus tramadol. J R Soc Med 1999; 92(9): 474–5PubMed
149.
Zurück zum Zitat Lin JH, Yamazaki M. Clinical relevance of P-glycoprotein in drug therapy. Drug Metab Rev 2003; 35(4): 417–54PubMedCrossRef Lin JH, Yamazaki M. Clinical relevance of P-glycoprotein in drug therapy. Drug Metab Rev 2003; 35(4): 417–54PubMedCrossRef
150.
Zurück zum Zitat Lin JH, Yamazaki M. Role of P-glycoprotein in pharmacokinetics: clinical implications. Clin Pharmacokinet 2003; 42(1): 59–98PubMedCrossRef Lin JH, Yamazaki M. Role of P-glycoprotein in pharmacokinetics: clinical implications. Clin Pharmacokinet 2003; 42(1): 59–98PubMedCrossRef
151.
Zurück zum Zitat Levy RH. Metabolic drug interactions. Philadelphia: Lippincott Williams & Wilkins, 2005 Levy RH. Metabolic drug interactions. Philadelphia: Lippincott Williams & Wilkins, 2005
152.
Zurück zum Zitat Lin JH, Lu AY. Inhibition and induction of cytochrome P450 and the clinical implications. Clin Pharmacokinet 1998; 35(5): 361–90PubMedCrossRef Lin JH, Lu AY. Inhibition and induction of cytochrome P450 and the clinical implications. Clin Pharmacokinet 1998; 35(5): 361–90PubMedCrossRef
153.
Zurück zum Zitat Olesen OV, Linnet K. Fluvoxamine-clozapine drug interaction: inhibition in vitro of five cytochrome P450 isoforms involved in clozapine metabolism. J Clin Psychopharmacol 2000; 20(1): 35–42PubMedCrossRef Olesen OV, Linnet K. Fluvoxamine-clozapine drug interaction: inhibition in vitro of five cytochrome P450 isoforms involved in clozapine metabolism. J Clin Psychopharmacol 2000; 20(1): 35–42PubMedCrossRef
154.
Zurück zum Zitat Fang J, Coutts RT, McKenna KF, et al. Elucidation of individual cytochrome P450 enzymes involved in the metabolism of clozapine. Naunyn Schmiedebergs Arch Pharmacol 1998; 358(5): 592–9PubMedCrossRef Fang J, Coutts RT, McKenna KF, et al. Elucidation of individual cytochrome P450 enzymes involved in the metabolism of clozapine. Naunyn Schmiedebergs Arch Pharmacol 1998; 358(5): 592–9PubMedCrossRef
155.
Zurück zum Zitat Eiermann B, Engel G, Johansson I, et al. The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapine. Br J Clin Pharmacol 1997; 44: 439–46PubMedCrossRef Eiermann B, Engel G, Johansson I, et al. The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapine. Br J Clin Pharmacol 1997; 44: 439–46PubMedCrossRef
156.
Zurück zum Zitat Wienkers LC, Heath TG. Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov 2005; 4(10): 825–33PubMedCrossRef Wienkers LC, Heath TG. Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov 2005; 4(10): 825–33PubMedCrossRef
157.
Zurück zum Zitat Bertz RJ, Granneman GR. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997; 32(3): 210–58PubMedCrossRef Bertz RJ, Granneman GR. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997; 32(3): 210–58PubMedCrossRef
158.
Zurück zum Zitat Bonnabry P, Sievering J, Leemann T, et al. Quantitative drug interactions prediction system (Q-DIPS): a dynamic computerbased method to assist in the choice of clinically relevant in vivo studies. Clin Pharmacokinet 2001; 40(9): 631–40PubMedCrossRef Bonnabry P, Sievering J, Leemann T, et al. Quantitative drug interactions prediction system (Q-DIPS): a dynamic computerbased method to assist in the choice of clinically relevant in vivo studies. Clin Pharmacokinet 2001; 40(9): 631–40PubMedCrossRef
159.
Zurück zum Zitat Lin JH, Lu AY. Interindividual variability in inhibition and induction of cytochrome P450 enzymes. Annu Rev Pharmacol Toxicol 2001; 41: 535–67PubMedCrossRef Lin JH, Lu AY. Interindividual variability in inhibition and induction of cytochrome P450 enzymes. Annu Rev Pharmacol Toxicol 2001; 41: 535–67PubMedCrossRef
160.
Zurück zum Zitat Schmider J, Von Moltke LL, Shader RI, et al. Extrapolating in vitro data on drug metabolism to in vivo pharmacokinetics: evaluation of the pharmacokinetic interaction between amitriptyline and fluoxetine. Drug Metab Rev 1999; 31(2): 545–60PubMedCrossRef Schmider J, Von Moltke LL, Shader RI, et al. Extrapolating in vitro data on drug metabolism to in vivo pharmacokinetics: evaluation of the pharmacokinetic interaction between amitriptyline and fluoxetine. Drug Metab Rev 1999; 31(2): 545–60PubMedCrossRef
161.
Zurück zum Zitat Obach RS, Walsky RL, Venkatakrishnan K, et al. In vitro cytochrome P450 inhibition data and the prediction of drug-drug interactions: qualitative relationships, quantitative predictions, and the rank-order approach. Clin Pharmacol Ther 2005; 78(6): 582–92PubMedCrossRef Obach RS, Walsky RL, Venkatakrishnan K, et al. In vitro cytochrome P450 inhibition data and the prediction of drug-drug interactions: qualitative relationships, quantitative predictions, and the rank-order approach. Clin Pharmacol Ther 2005; 78(6): 582–92PubMedCrossRef
162.
Zurück zum Zitat Obach RS, Walsky RL, Venkatakrishnan K, et al. The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions. J Pharmacol Exp Ther 2006; 316(1): 336–48PubMedCrossRef Obach RS, Walsky RL, Venkatakrishnan K, et al. The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions. J Pharmacol Exp Ther 2006; 316(1): 336–48PubMedCrossRef
163.
Zurück zum Zitat Lane R, Baldwin D. Selective serotonin reuptake inhibitor-induced serotonin syndrome: review. J Clin Psychopharmacol 1997; 17(3): 208–21PubMedCrossRef Lane R, Baldwin D. Selective serotonin reuptake inhibitor-induced serotonin syndrome: review. J Clin Psychopharmacol 1997; 17(3): 208–21PubMedCrossRef
164.
Zurück zum Zitat Morales N, Vermette H. Serotonin syndrome associated with linezolid treatment after discontinuation of fluoxetine. Psychosomatics 2005; 46(3): 274–5PubMedCrossRef Morales N, Vermette H. Serotonin syndrome associated with linezolid treatment after discontinuation of fluoxetine. Psychosomatics 2005; 46(3): 274–5PubMedCrossRef
165.
Zurück zum Zitat Bhatara VS, Magnus RD, Paul KL, et al. Serotonin syndrome induced by venlafaxine and fluoxetine: a case study in polypharmacy and potential pharmacodynamic and pharmacokinetic mechanisms. Ann Pharmacother 1998; 32(4): 432–6PubMedCrossRef Bhatara VS, Magnus RD, Paul KL, et al. Serotonin syndrome induced by venlafaxine and fluoxetine: a case study in polypharmacy and potential pharmacodynamic and pharmacokinetic mechanisms. Ann Pharmacother 1998; 32(4): 432–6PubMedCrossRef
166.
Zurück zum Zitat Coplan JD, Gorman JM. Detectable levels of fluoxetine metabolites after discontinuation: an unexpected serotonin syndrome. Am J Psychiatry 1993; 150(5): 837PubMed Coplan JD, Gorman JM. Detectable levels of fluoxetine metabolites after discontinuation: an unexpected serotonin syndrome. Am J Psychiatry 1993; 150(5): 837PubMed
167.
Zurück zum Zitat Ciraulo DA, Shader RI, Greenblatt DJ, et al. Basic concepts. In: Ciraulo DA, Shader RI, Greenblatt DJ, et al., editors. Drug interactions in psychiatry. Maryland, USA: Williams & Wilkins, 1995: 1–28 Ciraulo DA, Shader RI, Greenblatt DJ, et al. Basic concepts. In: Ciraulo DA, Shader RI, Greenblatt DJ, et al., editors. Drug interactions in psychiatry. Maryland, USA: Williams & Wilkins, 1995: 1–28
168.
Zurück zum Zitat Saito M, Yasui-Furukori N, Nakagami T, et al. Dose-dependent interaction of paroxetine with risperidone in schizophrenic patients. J Clin Psychopharmacol 2005; 25(6): 527–32PubMedCrossRef Saito M, Yasui-Furukori N, Nakagami T, et al. Dose-dependent interaction of paroxetine with risperidone in schizophrenic patients. J Clin Psychopharmacol 2005; 25(6): 527–32PubMedCrossRef
169.
Zurück zum Zitat Paus E, Jonzier-Perey M, Cochard N, et al. Chirality in the new generation of antidepressants: stereoselective analysis of the enantiomers of mirtazapine, N-demethylmirtazapine, and 8-hydroxymirtazapine by LC-MS. Ther Drug Monit 2004; 26(4): 366–74PubMedCrossRef Paus E, Jonzier-Perey M, Cochard N, et al. Chirality in the new generation of antidepressants: stereoselective analysis of the enantiomers of mirtazapine, N-demethylmirtazapine, and 8-hydroxymirtazapine by LC-MS. Ther Drug Monit 2004; 26(4): 366–74PubMedCrossRef
170.
Zurück zum Zitat Bondolfi G, Chautems C, Rochat B, et al. Non-response to citalopram in depressive patients: pharmacokinetic and clinical consequences of a fluvoxamine augmentation. Psychopharmacology (Berl) 1996; 128 (4): 421–5CrossRef Bondolfi G, Chautems C, Rochat B, et al. Non-response to citalopram in depressive patients: pharmacokinetic and clinical consequences of a fluvoxamine augmentation. Psychopharmacology (Berl) 1996; 128 (4): 421–5CrossRef
171.
Zurück zum Zitat Bondolfi G, Lissner C, Kosel M, et al. Fluoxetine augmentation in citalopram non-responders: pharmacokinetic and clinical consequences. Int J Neuropsychopharmacol 2000; 3(1): 55–60PubMedCrossRef Bondolfi G, Lissner C, Kosel M, et al. Fluoxetine augmentation in citalopram non-responders: pharmacokinetic and clinical consequences. Int J Neuropsychopharmacol 2000; 3(1): 55–60PubMedCrossRef
172.
Zurück zum Zitat Eap CB, Bertel-Laubscher R, Zullino D, et al. Marked increase of venlafaxine enantiomer concentrations as a consequence of metabolic interactions: a case report. Pharmacopsychiatry 2000; 33(3): 112–5PubMedCrossRef Eap CB, Bertel-Laubscher R, Zullino D, et al. Marked increase of venlafaxine enantiomer concentrations as a consequence of metabolic interactions: a case report. Pharmacopsychiatry 2000; 33(3): 112–5PubMedCrossRef
173.
Zurück zum Zitat Steinacher L, Vandel P, Zullino DF, et al. Carbamazepine augmentation in depressive patients non-responding to citalopram: a pharmacokinetic and clinical pilot study. Eur Neuropsychopharmacol 2002; 12(3): 255–60PubMedCrossRef Steinacher L, Vandel P, Zullino DF, et al. Carbamazepine augmentation in depressive patients non-responding to citalopram: a pharmacokinetic and clinical pilot study. Eur Neuropsychopharmacol 2002; 12(3): 255–60PubMedCrossRef
174.
Zurück zum Zitat Gibaldi M. Stereoselective and isozyme-selective drug interactions. Chirality 1993; 5(6): 407–13PubMedCrossRef Gibaldi M. Stereoselective and isozyme-selective drug interactions. Chirality 1993; 5(6): 407–13PubMedCrossRef
175.
Zurück zum Zitat Gidal BE, Sorkness CA, McGill KA, et al. Evaluation of a potential enantioselective interaction between ticlopidine and warfarin in chronically anticoagulated patients. Ther Drug Monit 1995; 17(1): 33–8PubMedCrossRef Gidal BE, Sorkness CA, McGill KA, et al. Evaluation of a potential enantioselective interaction between ticlopidine and warfarin in chronically anticoagulated patients. Ther Drug Monit 1995; 17(1): 33–8PubMedCrossRef
176.
Zurück zum Zitat Ciusani E, Zullino DF, Eap CB, et al. Combination therapy with venlafaxine and carbamazepine in depressive patients not responding to venlafaxine: pharmacokinetic and clinical aspects. J Psychopharmacol 2004; 18(4): 559–66PubMedCrossRef Ciusani E, Zullino DF, Eap CB, et al. Combination therapy with venlafaxine and carbamazepine in depressive patients not responding to venlafaxine: pharmacokinetic and clinical aspects. J Psychopharmacol 2004; 18(4): 559–66PubMedCrossRef
177.
Zurück zum Zitat Zhou Q, Chan E. Effect of omeprazole on the anticoagulant activity and the pharmacokinetics of warfarin enantiomers in rats. Eur J Pharm Sci 2003; 20(4-5): 439–49PubMedCrossRef Zhou Q, Chan E. Effect of omeprazole on the anticoagulant activity and the pharmacokinetics of warfarin enantiomers in rats. Eur J Pharm Sci 2003; 20(4-5): 439–49PubMedCrossRef
178.
Zurück zum Zitat Andersson T, Hassan-Alin M, Hasselgren G, et al. Drug interaction studies with esomeprazole, the (S)-isomer of omeprazole. Clin Pharmacokinet 2001; 40(7): 523–37PubMedCrossRef Andersson T, Hassan-Alin M, Hasselgren G, et al. Drug interaction studies with esomeprazole, the (S)-isomer of omeprazole. Clin Pharmacokinet 2001; 40(7): 523–37PubMedCrossRef
179.
Zurück zum Zitat Knezevic B, Ramseier F, Jaquenoud Sirot E. Clozapine-fluvoxamine combination therapy: how much fluvoxamine? Results from a case series. Eur Psychiatry 2006; 21: S225 Knezevic B, Ramseier F, Jaquenoud Sirot E. Clozapine-fluvoxamine combination therapy: how much fluvoxamine? Results from a case series. Eur Psychiatry 2006; 21: S225
180.
Zurück zum Zitat Armstrong SC, Stephans JR. Blood clozapine levels elevated by fluvoxamine: potential for side effects and lower clozapine dosage. J Clin Psychiatry 1997; 58(11): 499PubMedCrossRef Armstrong SC, Stephans JR. Blood clozapine levels elevated by fluvoxamine: potential for side effects and lower clozapine dosage. J Clin Psychiatry 1997; 58(11): 499PubMedCrossRef
181.
Zurück zum Zitat Lu ML, Lane HY, Lin SK, et al. Adjunctive fluvoxamine inhibits clozapine-related weight gain and metabolic disturbances. J Clin Psychiatry 2004; 65(6): 766–71PubMedCrossRef Lu ML, Lane HY, Lin SK, et al. Adjunctive fluvoxamine inhibits clozapine-related weight gain and metabolic disturbances. J Clin Psychiatry 2004; 65(6): 766–71PubMedCrossRef
182.
Zurück zum Zitat Silver H, Kaplan A, Jahjah N. Fluvoxamine augmentation for clozapine-resistant schizophrenia. Am J Psychiatry 1995; 152(7): 1098PubMed Silver H, Kaplan A, Jahjah N. Fluvoxamine augmentation for clozapine-resistant schizophrenia. Am J Psychiatry 1995; 152(7): 1098PubMed
183.
Zurück zum Zitat Szegedi A, Anghelescu I, Wiesner J, et al. Addition of low-dose fluvoxamine to low-dose clozapine monotherapy in schizophrenia: drug monitoring and tolerability data from a prospective clinical trial. Pharmacopsychiatry 1999; 32(4): 148–53PubMedCrossRef Szegedi A, Anghelescu I, Wiesner J, et al. Addition of low-dose fluvoxamine to low-dose clozapine monotherapy in schizophrenia: drug monitoring and tolerability data from a prospective clinical trial. Pharmacopsychiatry 1999; 32(4): 148–53PubMedCrossRef
184.
Zurück zum Zitat Wetzel H, Anghelescu I, Szegedi A, et al. Pharmacokinetic interactions of clozapine with selective serotonin reuptake inhibitors: differential effects of fluvoxamine and paroxetine in a prospective study. J Clin Psychopharmacol 1998; 18(1): 2–9PubMedCrossRef Wetzel H, Anghelescu I, Szegedi A, et al. Pharmacokinetic interactions of clozapine with selective serotonin reuptake inhibitors: differential effects of fluvoxamine and paroxetine in a prospective study. J Clin Psychopharmacol 1998; 18(1): 2–9PubMedCrossRef
185.
Zurück zum Zitat Silver H. Fluvoxamine as an adjunctive agent in schizophrenia. CNS Drug Rev 2001; 7(3): 283–304PubMedCrossRef Silver H. Fluvoxamine as an adjunctive agent in schizophrenia. CNS Drug Rev 2001; 7(3): 283–304PubMedCrossRef
186.
Zurück zum Zitat Fabrazzo M, La Pia S, Monteleone P, et al. Fluvoxamine increases plasma and urinary levels of clozapine and its major metabolites in a time- and dose-dependent manner. J Clin Psychopharmacol 2000; 20(6): 708–10PubMedCrossRef Fabrazzo M, La Pia S, Monteleone P, et al. Fluvoxamine increases plasma and urinary levels of clozapine and its major metabolites in a time- and dose-dependent manner. J Clin Psychopharmacol 2000; 20(6): 708–10PubMedCrossRef
187.
Zurück zum Zitat Christensen M, Tybring G, Mihara K, et al. Low daily 10mg and 20mg doses of fluvoxamine inhibit the metabolism of both caffeine (cytochrome P4501A2) and omeprazole (cytochrome P4502C19). Clin Pharmacol Ther 2002; 71(3): 141–52PubMedCrossRef Christensen M, Tybring G, Mihara K, et al. Low daily 10mg and 20mg doses of fluvoxamine inhibit the metabolism of both caffeine (cytochrome P4501A2) and omeprazole (cytochrome P4502C19). Clin Pharmacol Ther 2002; 71(3): 141–52PubMedCrossRef
188.
Zurück zum Zitat Clarke SM, Mulcahy FM, Tjia J, et al. The pharmacokinetics of methadone in HIV-positive patients receiving the non-nucleoside reverse transcriptase inhibitor efavirenz. Br J Clin Pharmacol 2001; 51(3): 213–7PubMedCrossRef Clarke SM, Mulcahy FM, Tjia J, et al. The pharmacokinetics of methadone in HIV-positive patients receiving the non-nucleoside reverse transcriptase inhibitor efavirenz. Br J Clin Pharmacol 2001; 51(3): 213–7PubMedCrossRef
189.
Zurück zum Zitat Eap CB, Buclin T, Baumann P. Interindividual variability of the clinical pharmacokinetics of methadone: implications for the treatment of opioid dependence. Clin Pharmacokinet 2002; 41(14): 1153–1193PubMedCrossRef Eap CB, Buclin T, Baumann P. Interindividual variability of the clinical pharmacokinetics of methadone: implications for the treatment of opioid dependence. Clin Pharmacokinet 2002; 41(14): 1153–1193PubMedCrossRef
190.
Zurück zum Zitat Marzolini C, Troillet N, Telenti A, et al. Efavirenz decreases methadone blood concentrations. AIDS 2000; 14(9): 1291–2PubMedCrossRef Marzolini C, Troillet N, Telenti A, et al. Efavirenz decreases methadone blood concentrations. AIDS 2000; 14(9): 1291–2PubMedCrossRef
191.
Zurück zum Zitat Clarke SM, Mulcahy FM, Tjia J, et al. Pharmacokinetic interactions of nevirapine and methadone and guidelines for use of nevirapine to treat injection drug users. Clin Infect Dis 2001; 33(9): 1595–7PubMedCrossRef Clarke SM, Mulcahy FM, Tjia J, et al. Pharmacokinetic interactions of nevirapine and methadone and guidelines for use of nevirapine to treat injection drug users. Clin Infect Dis 2001; 33(9): 1595–7PubMedCrossRef
192.
Zurück zum Zitat Faber MS, Fuhr U. Time response of cytochrome P450 1A2 activity on cessation of heavy smoking. Clin Pharmacol Ther 2004; 76(2): 178–84PubMedCrossRef Faber MS, Fuhr U. Time response of cytochrome P450 1A2 activity on cessation of heavy smoking. Clin Pharmacol Ther 2004; 76(2): 178–84PubMedCrossRef
193.
Zurück zum Zitat Cozza KL, Armstrong SC, Oesterheld JR. Concise guide to drug interaction principles for medical practice. 2nd ed. Arlington (VA): American Psychiatric Publishing, Inc., 2003 Cozza KL, Armstrong SC, Oesterheld JR. Concise guide to drug interaction principles for medical practice. 2nd ed. Arlington (VA): American Psychiatric Publishing, Inc., 2003
194.
Zurück zum Zitat Yue QY, Tomson T, Sawe J. Carbamazepine and cigarette smoking induce differentially the metabolism of codeine in man. Pharmacogenetics 1994; 4(4): 193–8PubMedCrossRef Yue QY, Tomson T, Sawe J. Carbamazepine and cigarette smoking induce differentially the metabolism of codeine in man. Pharmacogenetics 1994; 4(4): 193–8PubMedCrossRef
195.
Zurück zum Zitat Bondolfi G, Morel F, Crettol S, et al. Increased clozapine plasma concentrations and side effects induced by smoking cessation in 2 CYP1A2 genotyped patients. Ther Drug Monit 2005; 27(4): 539–43PubMedCrossRef Bondolfi G, Morel F, Crettol S, et al. Increased clozapine plasma concentrations and side effects induced by smoking cessation in 2 CYP1A2 genotyped patients. Ther Drug Monit 2005; 27(4): 539–43PubMedCrossRef
196.
Zurück zum Zitat de Leon J. Atypical antipsychotic dosing: the effect of smoking and caffeine. Psychiatr Serv 2004; 55(5): 491–3PubMedCrossRef de Leon J. Atypical antipsychotic dosing: the effect of smoking and caffeine. Psychiatr Serv 2004; 55(5): 491–3PubMedCrossRef
197.
Zurück zum Zitat Zullino DF, Delessert D, Eap CB, et al. Tobacco and cannabis smoking cessation can lead to intoxication with clozapine or olanzapine. Int Clin Psychopharmacol 2002; 17(3): 141–3PubMedCrossRef Zullino DF, Delessert D, Eap CB, et al. Tobacco and cannabis smoking cessation can lead to intoxication with clozapine or olanzapine. Int Clin Psychopharmacol 2002; 17(3): 141–3PubMedCrossRef
198.
Zurück zum Zitat Carrillo JA, Herraiz AG, Ramos SI, et al. Role of the smokinginduced cytochrome P450 (CYP)1A2 and polymorphic CYP2D6 in steady-state concentration of olanzapine. J Clin Psychopharmacol 2003; 23(2): 119–27PubMedCrossRef Carrillo JA, Herraiz AG, Ramos SI, et al. Role of the smokinginduced cytochrome P450 (CYP)1A2 and polymorphic CYP2D6 in steady-state concentration of olanzapine. J Clin Psychopharmacol 2003; 23(2): 119–27PubMedCrossRef
199.
Zurück zum Zitat Saito M, Hirata-Koizumi M, Matsumoto M, et al. Undesirable effects of citrus juice on the pharmacokinetics of drugs: focus on recent studies. Drug Saf 2005; 28(8): 677–94PubMedCrossRef Saito M, Hirata-Koizumi M, Matsumoto M, et al. Undesirable effects of citrus juice on the pharmacokinetics of drugs: focus on recent studies. Drug Saf 2005; 28(8): 677–94PubMedCrossRef
200.
Zurück zum Zitat Bailey DG, Dresser GK. Interactions between grapefruit juice and cardiovascular drugs. Am J Cardiovasc Drugs 2004; 4(5): 281–97PubMedCrossRef Bailey DG, Dresser GK. Interactions between grapefruit juice and cardiovascular drugs. Am J Cardiovasc Drugs 2004; 4(5): 281–97PubMedCrossRef
201.
Zurück zum Zitat Dahan A, Altman H. Food-drug interaction: grapefruit juice augments drug bioavailability: mechanism, extent and relevance. Eur J Clin Nutr 2004; 58(1): 1–9PubMedCrossRef Dahan A, Altman H. Food-drug interaction: grapefruit juice augments drug bioavailability: mechanism, extent and relevance. Eur J Clin Nutr 2004; 58(1): 1–9PubMedCrossRef
202.
Zurück zum Zitat Martin J, Krum H. Cytochrome P450 drug interactions within the HMG-CoA reductase inhibitor class: are they clinically relevant? Drug Saf 2003; 26(1): 13–21PubMedCrossRef Martin J, Krum H. Cytochrome P450 drug interactions within the HMG-CoA reductase inhibitor class: are they clinically relevant? Drug Saf 2003; 26(1): 13–21PubMedCrossRef
203.
Zurück zum Zitat Harris RZ, Jang GR, Tsunoda S. Dietary effects on drug metabolism and transport. Clin Pharmacokinet 2003; 42(13): 1071–88PubMedCrossRef Harris RZ, Jang GR, Tsunoda S. Dietary effects on drug metabolism and transport. Clin Pharmacokinet 2003; 42(13): 1071–88PubMedCrossRef
204.
Zurück zum Zitat Mills E, Wu P, Johnston BC, et al. Natural health product-drug interactions: a systematic review of clinical trials. Ther Drug Monit 2005; 27(5): 549–57PubMedCrossRef Mills E, Wu P, Johnston BC, et al. Natural health product-drug interactions: a systematic review of clinical trials. Ther Drug Monit 2005; 27(5): 549–57PubMedCrossRef
205.
Zurück zum Zitat Carrillo JA, Herraiz AG, Ramos SI, et al. Effects of caffeine withdrawal from the diet on the metabolism of clozapine in schizophrenic patients. J Clin Psychopharmacol 1998; 18(4): 311–6PubMedCrossRef Carrillo JA, Herraiz AG, Ramos SI, et al. Effects of caffeine withdrawal from the diet on the metabolism of clozapine in schizophrenic patients. J Clin Psychopharmacol 1998; 18(4): 311–6PubMedCrossRef
206.
Zurück zum Zitat Raaska K, Raitasuo V, Laitila J, et al. Effect of caffeine-containing versus decaffeinated coffee on serum clozapine concentrations in hospitalised patients. Basic Clin Pharmacol Toxicol 2004; 94(1): 13–8PubMedCrossRef Raaska K, Raitasuo V, Laitila J, et al. Effect of caffeine-containing versus decaffeinated coffee on serum clozapine concentrations in hospitalised patients. Basic Clin Pharmacol Toxicol 2004; 94(1): 13–8PubMedCrossRef
207.
Zurück zum Zitat Ferrari AR, Guerrini R, Gatti G, et al. Influence of dosage, age, and co-medication on plasma topiramate concentrations in children and adults with severe epilepsy and preliminary observations on correlations with clinical response. Ther Drug Monit 2003; 25(6): 700–8PubMedCrossRef Ferrari AR, Guerrini R, Gatti G, et al. Influence of dosage, age, and co-medication on plasma topiramate concentrations in children and adults with severe epilepsy and preliminary observations on correlations with clinical response. Ther Drug Monit 2003; 25(6): 700–8PubMedCrossRef
208.
Zurück zum Zitat Gatti G, Ferrari AR, Guerrini R, et al. Plasma gabapentin concentrations in children with epilepsy: influence of age, relationship with dosage, and preliminary observations on correlation with clinical response. Ther Drug Monit 2003; 25(1): 54–60PubMedCrossRef Gatti G, Ferrari AR, Guerrini R, et al. Plasma gabapentin concentrations in children with epilepsy: influence of age, relationship with dosage, and preliminary observations on correlation with clinical response. Ther Drug Monit 2003; 25(1): 54–60PubMedCrossRef
209.
Zurück zum Zitat Pollock BG. The pharmacokinetic imperative in late-life depression. J Clin Psychopharmacol 2005; 25(4 Suppl. 1): S19–23PubMedCrossRef Pollock BG. The pharmacokinetic imperative in late-life depression. J Clin Psychopharmacol 2005; 25(4 Suppl. 1): S19–23PubMedCrossRef
210.
Zurück zum Zitat Cotreau MM, Von Moltke LL, Greenblatt DJ. The influence of age and sex on the clearance of cytochrome P450 3A substrates. Clin Pharmacokinet 2005; 44(1): 33–60PubMedCrossRef Cotreau MM, Von Moltke LL, Greenblatt DJ. The influence of age and sex on the clearance of cytochrome P450 3A substrates. Clin Pharmacokinet 2005; 44(1): 33–60PubMedCrossRef
211.
Zurück zum Zitat Byerly MJ, Weber MT, Brooks DL, et al. Antipsychotic medications and the elderly: effects on cognition and implications for use. Drugs Aging 2001; 18(1): 45–61PubMedCrossRef Byerly MJ, Weber MT, Brooks DL, et al. Antipsychotic medications and the elderly: effects on cognition and implications for use. Drugs Aging 2001; 18(1): 45–61PubMedCrossRef
212.
Zurück zum Zitat Barbui C, Nose M, Bindman J, et al. Sex differences in the subjective tolerability of antipsychotic drugs. J Clin Psychopharmacol 2005; 25(6): 521–6PubMedCrossRef Barbui C, Nose M, Bindman J, et al. Sex differences in the subjective tolerability of antipsychotic drugs. J Clin Psychopharmacol 2005; 25(6): 521–6PubMedCrossRef
213.
Zurück zum Zitat Clark R. Sex differences in antiretroviral therapy-associated intolerance and adverse events. Drug Saf 2005; 28(12): 1075–83PubMedCrossRef Clark R. Sex differences in antiretroviral therapy-associated intolerance and adverse events. Drug Saf 2005; 28(12): 1075–83PubMedCrossRef
214.
Zurück zum Zitat Seeman MV. Gender differences in the prescribing of antipsychotic drugs. Am J Psychiatry 2004; 161(8): 1324–33PubMedCrossRef Seeman MV. Gender differences in the prescribing of antipsychotic drugs. Am J Psychiatry 2004; 161(8): 1324–33PubMedCrossRef
215.
Zurück zum Zitat Rademaker M. Do women have more adverse drug reactions? Am J Clin Dermatol 2001; 2(6): 349–51PubMedCrossRef Rademaker M. Do women have more adverse drug reactions? Am J Clin Dermatol 2001; 2(6): 349–51PubMedCrossRef
216.
Zurück zum Zitat Jaquenoud Sirot E, Eap CBBP. Follow-up study using TDM and pharmacogenetic testing as tools in pharmacovigilance [abstract]. Drug Saf 2004; 27(12): 937 Jaquenoud Sirot E, Eap CBBP. Follow-up study using TDM and pharmacogenetic testing as tools in pharmacovigilance [abstract]. Drug Saf 2004; 27(12): 937
217.
Zurück zum Zitat Pollock BG. Gender differences in psychotropic drug metabolism. Psychopharmacol Bull 1997; 33(2): 235–41PubMed Pollock BG. Gender differences in psychotropic drug metabolism. Psychopharmacol Bull 1997; 33(2): 235–41PubMed
218.
Zurück zum Zitat Perry PJ, Bever KA, Arndt S, et al. Relationship between patient variables and plasma clozapine concentrations: a dosing nomogram. Biol Psychiatry 1998; 44(8): 733–8PubMedCrossRef Perry PJ, Bever KA, Arndt S, et al. Relationship between patient variables and plasma clozapine concentrations: a dosing nomogram. Biol Psychiatry 1998; 44(8): 733–8PubMedCrossRef
219.
Zurück zum Zitat Lane HY, Chang YC, Chang WH, et al. Effects of gender and age on plasma levels of clozapine and its metabolites: analyzed by critical statistics. J Clin Psychiatry 1999; 60(1): 36–40PubMedCrossRef Lane HY, Chang YC, Chang WH, et al. Effects of gender and age on plasma levels of clozapine and its metabolites: analyzed by critical statistics. J Clin Psychiatry 1999; 60(1): 36–40PubMedCrossRef
220.
Zurück zum Zitat Weiss U, Marksteiner J, Kemmler G, et al. Effects of age and sex on olanzapine plasma concentrations. J Clin Psychopharmacol 2005; 25(6): 570–4PubMedCrossRef Weiss U, Marksteiner J, Kemmler G, et al. Effects of age and sex on olanzapine plasma concentrations. J Clin Psychopharmacol 2005; 25(6): 570–4PubMedCrossRef
221.
Zurück zum Zitat Beierle I, Meibohm B, Derendorf H. Gender differences in pharmacokinetics and pharmacodynamics. Int J Clin Pharmacol Ther 1999; 37(11): 529–47PubMed Beierle I, Meibohm B, Derendorf H. Gender differences in pharmacokinetics and pharmacodynamics. Int J Clin Pharmacol Ther 1999; 37(11): 529–47PubMed
222.
Zurück zum Zitat Meibohm B, Beierle I, Derendorf H. How important are gender differences in pharmacokinetics? Clin Pharmacokinet 2002; 41(5): 329–42PubMedCrossRef Meibohm B, Beierle I, Derendorf H. How important are gender differences in pharmacokinetics? Clin Pharmacokinet 2002; 41(5): 329–42PubMedCrossRef
223.
Zurück zum Zitat Hagg S, Spigset O, Dahlqvist R. Influence of gender and oral contraceptives on CYP2D6 and CYP2C19 activity in healthy volunteers. Br J Clin Pharmacol 2001; 51(2): 169–73PubMedCrossRef Hagg S, Spigset O, Dahlqvist R. Influence of gender and oral contraceptives on CYP2D6 and CYP2C19 activity in healthy volunteers. Br J Clin Pharmacol 2001; 51(2): 169–73PubMedCrossRef
224.
Zurück zum Zitat Hutson WR, Roehrkasse RL, Wald A. Influence of gender and menopause on gastric emptying and motility. Gastroenterology 1989; 96(1): 11–7PubMed Hutson WR, Roehrkasse RL, Wald A. Influence of gender and menopause on gastric emptying and motility. Gastroenterology 1989; 96(1): 11–7PubMed
225.
Zurück zum Zitat Haack MJ, Bak ML, Beurskens R, et al. Toxic rise of clozapine plasma concentrations in relation to inflammation. Eur Neuropsychopharmacol 2003; 13(5): 381–5PubMedCrossRef Haack MJ, Bak ML, Beurskens R, et al. Toxic rise of clozapine plasma concentrations in relation to inflammation. Eur Neuropsychopharmacol 2003; 13(5): 381–5PubMedCrossRef
226.
Zurück zum Zitat Raaska K, Raitasuo V, Arstila M, et al. Bacterial pneumonia can increase serum concentration of clozapine. Eur J Clin Pharmacol 2002; 58(5): 321–2PubMedCrossRef Raaska K, Raitasuo V, Arstila M, et al. Bacterial pneumonia can increase serum concentration of clozapine. Eur J Clin Pharmacol 2002; 58(5): 321–2PubMedCrossRef
227.
Zurück zum Zitat Bleau AM, Maurel P, Pichette V, et al. Interleukin-1beta, interleukin- 6, tumour necrosis factor-alpha and interferon-gamma released by a viral infection and an aseptic inflammation reduce CYP1A1, 1A2 and 3A6 expression in rabbit hepatocytes. Eur J Pharmacol 2003; 473(2-3): 197–206PubMedCrossRef Bleau AM, Maurel P, Pichette V, et al. Interleukin-1beta, interleukin- 6, tumour necrosis factor-alpha and interferon-gamma released by a viral infection and an aseptic inflammation reduce CYP1A1, 1A2 and 3A6 expression in rabbit hepatocytes. Eur J Pharmacol 2003; 473(2-3): 197–206PubMedCrossRef
228.
Zurück zum Zitat Crawford JH, Yang S, Zhou M, et al. Down-regulation of hepatic CYP1A2 plays an important role in inflammatory responses in sepsis. Crit Care Med 2004; 32(2): 502–8PubMedCrossRef Crawford JH, Yang S, Zhou M, et al. Down-regulation of hepatic CYP1A2 plays an important role in inflammatory responses in sepsis. Crit Care Med 2004; 32(2): 502–8PubMedCrossRef
229.
Zurück zum Zitat Aitken AE, Richardson TA, Morgan ET. Regulation of drug metabolizing enzymes and transporters in inflammation. Annu Rev Pharmacol Toxicol 2006; 46: 123–49PubMedCrossRef Aitken AE, Richardson TA, Morgan ET. Regulation of drug metabolizing enzymes and transporters in inflammation. Annu Rev Pharmacol Toxicol 2006; 46: 123–49PubMedCrossRef
230.
Zurück zum Zitat Richardson TA, Morgan ET. Hepatic cytochrome P450 gene regulation during endotoxin-induced inflammation in nuclear receptor knockout mice. J Pharmacol Exp Ther 2005; 314(2): 703–9PubMedCrossRef Richardson TA, Morgan ET. Hepatic cytochrome P450 gene regulation during endotoxin-induced inflammation in nuclear receptor knockout mice. J Pharmacol Exp Ther 2005; 314(2): 703–9PubMedCrossRef
231.
Zurück zum Zitat Wolkenstein P, Loriot MA, Aractingi S, et al. Prospective evaluation of detoxification pathways as markers of cutaneous adverse reactions to sulphonamides in AIDS. Pharmacogenetics 2000; 10(9): 821–8PubMedCrossRef Wolkenstein P, Loriot MA, Aractingi S, et al. Prospective evaluation of detoxification pathways as markers of cutaneous adverse reactions to sulphonamides in AIDS. Pharmacogenetics 2000; 10(9): 821–8PubMedCrossRef
232.
Zurück zum Zitat Meisel P. Arylamine N-acetyltransferases and drug response. Pharmacogenomics 2002; 3(3): 349–66PubMedCrossRef Meisel P. Arylamine N-acetyltransferases and drug response. Pharmacogenomics 2002; 3(3): 349–66PubMedCrossRef
233.
Zurück zum Zitat Wormhoudt LW, Commandeur JN, Vermeulen NP. Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity. Crit Rev Toxicol 1999; 29(1): 59–124PubMedCrossRef Wormhoudt LW, Commandeur JN, Vermeulen NP. Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity. Crit Rev Toxicol 1999; 29(1): 59–124PubMedCrossRef
234.
Zurück zum Zitat Liston HL, Markowitz JS, DeVane CL. Drug glucuronidation in clinical psychopharmacology. J Clin Psychopharmacol 2001; 21(5): 500–15PubMedCrossRef Liston HL, Markowitz JS, DeVane CL. Drug glucuronidation in clinical psychopharmacology. J Clin Psychopharmacol 2001; 21(5): 500–15PubMedCrossRef
235.
Zurück zum Zitat Hayes JD, Strange RC. Glutathione S-transferase polymorphisms and their biological consequences. Pharmacology 2000; 61: 154–66PubMedCrossRef Hayes JD, Strange RC. Glutathione S-transferase polymorphisms and their biological consequences. Pharmacology 2000; 61: 154–66PubMedCrossRef
236.
Zurück zum Zitat Dorne JLCM, Walton K, Renwick AG. Polymorphic CYP2C19 and N-acetylation: human variability in kinetics and pathway-related uncertainty factors. Food Chem Toxicol 2003; 41(2): 225–45PubMedCrossRef Dorne JLCM, Walton K, Renwick AG. Polymorphic CYP2C19 and N-acetylation: human variability in kinetics and pathway-related uncertainty factors. Food Chem Toxicol 2003; 41(2): 225–45PubMedCrossRef
237.
Zurück zum Zitat de Leon J. Glucuronidation enzymes, genes and psychiatry. Int J Neuropsychopharmacol 2003; 6: 57–72PubMedCrossRef de Leon J. Glucuronidation enzymes, genes and psychiatry. Int J Neuropsychopharmacol 2003; 6: 57–72PubMedCrossRef
238.
Zurück zum Zitat Burchell B. Genetic variation of human UDP-glucuronosyltransferase: implications in disease and drug glucuronidation. Am J Pharmacogenomics 2003; 3(1): 37–52PubMedCrossRef Burchell B. Genetic variation of human UDP-glucuronosyltransferase: implications in disease and drug glucuronidation. Am J Pharmacogenomics 2003; 3(1): 37–52PubMedCrossRef
239.
Zurück zum Zitat Miners JO, McKinnon RA, Mackenzie PI. Genetic polymorphisms of UDP-glucuronosyltransferases and their functional significance. Toxicology 2002; 181-2: 453–6CrossRef Miners JO, McKinnon RA, Mackenzie PI. Genetic polymorphisms of UDP-glucuronosyltransferases and their functional significance. Toxicology 2002; 181-2: 453–6CrossRef
240.
Zurück zum Zitat Burchell B, Hume R. Molecular genetic basis of Gilbert’s syndrome. J Gastroenterol Hepatol 1999; 14(10): 960–6PubMedCrossRef Burchell B, Hume R. Molecular genetic basis of Gilbert’s syndrome. J Gastroenterol Hepatol 1999; 14(10): 960–6PubMedCrossRef
241.
Zurück zum Zitat Premawardhena A, Fisher CA, Liu YT, et al. The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. Blood Cells Mol Dis 2003; 31(1): 98–101PubMedCrossRef Premawardhena A, Fisher CA, Liu YT, et al. The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. Blood Cells Mol Dis 2003; 31(1): 98–101PubMedCrossRef
242.
Zurück zum Zitat Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci U S A 1998; 95(14): 8170–4PubMedCrossRef Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci U S A 1998; 95(14): 8170–4PubMedCrossRef
243.
Zurück zum Zitat Iyer L, Ratain MJ. Pharmacogenetics and cancer chemotherapy. Eur J Cancer 1998; 34(10): 1493–9PubMedCrossRef Iyer L, Ratain MJ. Pharmacogenetics and cancer chemotherapy. Eur J Cancer 1998; 34(10): 1493–9PubMedCrossRef
244.
Zurück zum Zitat Iyer L, King CD, Whitington PF, et al. Genetic predisposition to the metabolism of irinotecan (CPT-11): role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes. J Clin Invest 1998; 101(4): 847–54PubMedCrossRef Iyer L, King CD, Whitington PF, et al. Genetic predisposition to the metabolism of irinotecan (CPT-11): role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes. J Clin Invest 1998; 101(4): 847–54PubMedCrossRef
245.
Zurück zum Zitat Strolin BM, Ruty B, Baltes E. Induction of endogenous pathways by antiepileptics and clinical implications. Fundam Clin Pharmacol 2005; 19(5): 511–29CrossRef Strolin BM, Ruty B, Baltes E. Induction of endogenous pathways by antiepileptics and clinical implications. Fundam Clin Pharmacol 2005; 19(5): 511–29CrossRef
246.
Zurück zum Zitat Anderson GD, Yau MK, Gidal BE, et al. Bidirectional interaction of valproate and lamotrigine in healthy subjects. Clin Pharmacol Ther 1996; 60(2): 145–56PubMedCrossRef Anderson GD, Yau MK, Gidal BE, et al. Bidirectional interaction of valproate and lamotrigine in healthy subjects. Clin Pharmacol Ther 1996; 60(2): 145–56PubMedCrossRef
247.
Zurück zum Zitat Page RL, O’Neil MG, Yarbrough DR, et al. Fatal toxic epidermal necrolysis related to lamotrigine administration. Pharmacotherapy 1998; 18(2): 392–8PubMed Page RL, O’Neil MG, Yarbrough DR, et al. Fatal toxic epidermal necrolysis related to lamotrigine administration. Pharmacotherapy 1998; 18(2): 392–8PubMed
248.
Zurück zum Zitat Johns LE, Houlston RS. N-acetyl transferase-2 and bladder cancer risk: a meta-analysis. Environ Mol Mutagen 2000; 36(3): 221–7PubMedCrossRef Johns LE, Houlston RS. N-acetyl transferase-2 and bladder cancer risk: a meta-analysis. Environ Mol Mutagen 2000; 36(3): 221–7PubMedCrossRef
249.
Zurück zum Zitat Green J, Banks E, Berrington A, et al. N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene-environment interaction. Br J Cancer 2000; 83(3): 412–7PubMedCrossRef Green J, Banks E, Berrington A, et al. N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene-environment interaction. Br J Cancer 2000; 83(3): 412–7PubMedCrossRef
250.
Zurück zum Zitat Spielberg SP. N-acetyltransferases: pharmacogenetics and clinical consequences of polymorphic drug metabolism. J Pharmacokinet Biopharm 1996; 24(5): 509–19PubMed Spielberg SP. N-acetyltransferases: pharmacogenetics and clinical consequences of polymorphic drug metabolism. J Pharmacokinet Biopharm 1996; 24(5): 509–19PubMed
251.
Zurück zum Zitat Hughes HB, BiehI JP, Jones A, et al. Metabolism of isoniazid in man as related to the occurrence of peripheral neuritis. Am Rev Tuberc 1954; 70(2): 266–73PubMed Hughes HB, BiehI JP, Jones A, et al. Metabolism of isoniazid in man as related to the occurrence of peripheral neuritis. Am Rev Tuberc 1954; 70(2): 266–73PubMed
252.
Zurück zum Zitat Lee W, Lockhart AC, Kim RB, et al. Cancer pharmacogenomics: powerful tools in cancer chemotherapy and drug development. Oncologist 2005; 10(2): 104–11PubMedCrossRef Lee W, Lockhart AC, Kim RB, et al. Cancer pharmacogenomics: powerful tools in cancer chemotherapy and drug development. Oncologist 2005; 10(2): 104–11PubMedCrossRef
253.
Zurück zum Zitat Al Hadithy AF, de Boer NK, Derijks LJ, et al. Thiopurines in inflammatory bowel disease: pharmacogenetics, therapeutic drug monitoring and clinical recommendations. Dig Liver Dis 2005; 37(4): 282–97PubMedCrossRef Al Hadithy AF, de Boer NK, Derijks LJ, et al. Thiopurines in inflammatory bowel disease: pharmacogenetics, therapeutic drug monitoring and clinical recommendations. Dig Liver Dis 2005; 37(4): 282–97PubMedCrossRef
254.
Zurück zum Zitat Yates CR, Krynetski EY, Loennechen T, et al. Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance. Ann Intern Med 1997; 126(8): 608–14PubMed Yates CR, Krynetski EY, Loennechen T, et al. Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance. Ann Intern Med 1997; 126(8): 608–14PubMed
255.
Zurück zum Zitat Collie-Duguid ES, Pritchard SC, Powrie RH, et al. The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. Pharmacogenetics 1999; 9(1): 37–42PubMedCrossRef Collie-Duguid ES, Pritchard SC, Powrie RH, et al. The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. Pharmacogenetics 1999; 9(1): 37–42PubMedCrossRef
256.
Zurück zum Zitat McLeod HL, Krynetski EY, Relling MV, et al. Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 2000; 14(4): 567–72PubMedCrossRef McLeod HL, Krynetski EY, Relling MV, et al. Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 2000; 14(4): 567–72PubMedCrossRef
257.
Zurück zum Zitat Schutz E, Gummert J, Mohr F, et al. Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient. Lancet 1993; 341(8842): 436PubMedCrossRef Schutz E, Gummert J, Mohr F, et al. Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient. Lancet 1993; 341(8842): 436PubMedCrossRef
258.
Zurück zum Zitat Coulthard SA, Matheson EC, Hall AG, et al. The clinical impact of thiopurine methyltransferase polymorphisms on thiopurine treatment. Nucleosides Nucleotides Nucleic Acids 2004; 23 (8-9): 1385–91CrossRef Coulthard SA, Matheson EC, Hall AG, et al. The clinical impact of thiopurine methyltransferase polymorphisms on thiopurine treatment. Nucleosides Nucleotides Nucleic Acids 2004; 23 (8-9): 1385–91CrossRef
259.
Zurück zum Zitat Evans WE. Pharmacogenetics of thiopurine S-methyltransferase and thiopurine therapy. Ther Drug Monit 2004; 26(2): 186–91PubMedCrossRef Evans WE. Pharmacogenetics of thiopurine S-methyltransferase and thiopurine therapy. Ther Drug Monit 2004; 26(2): 186–91PubMedCrossRef
260.
Zurück zum Zitat Krynetski E, Evans WE. Drug methylation in cancer therapy: lessons from the TPMT polymorphism. Oncogene 2003; 22(47): 7403–13PubMedCrossRef Krynetski E, Evans WE. Drug methylation in cancer therapy: lessons from the TPMT polymorphism. Oncogene 2003; 22(47): 7403–13PubMedCrossRef
261.
Zurück zum Zitat Spector R. Drug transport in the mammalian central nervous system: multiple complex systems: a critical analysis and commentary. Pharmacology 2000; 60(2): 58–73PubMedCrossRef Spector R. Drug transport in the mammalian central nervous system: multiple complex systems: a critical analysis and commentary. Pharmacology 2000; 60(2): 58–73PubMedCrossRef
262.
Zurück zum Zitat Doherty MM, Charman WN. The mucosa of the small intestine: how clinically relevant as an organ of drug metabolism? Clin Pharmacokinet 2002; 41(4): 235–53PubMedCrossRef Doherty MM, Charman WN. The mucosa of the small intestine: how clinically relevant as an organ of drug metabolism? Clin Pharmacokinet 2002; 41(4): 235–53PubMedCrossRef
263.
Zurück zum Zitat Uhr M, Steckler T, Yassouridis A, et al. Penetration of amitriptyline, but not of fluoxetine, into brain is enhanced in mice with blood-brain barrier deficiency due to mdr1a P-glycoprotein gene disruption. Neuropsychopharmacology 2000; 22(4): 380–7PubMedCrossRef Uhr M, Steckler T, Yassouridis A, et al. Penetration of amitriptyline, but not of fluoxetine, into brain is enhanced in mice with blood-brain barrier deficiency due to mdr1a P-glycoprotein gene disruption. Neuropsychopharmacology 2000; 22(4): 380–7PubMedCrossRef
264.
Zurück zum Zitat Roberts RL, Joyce PR, Mulder RT, et al. A common P-glycoprotein polymorphism is associated with nortriptyline-induced postural hypotension in patients treated for major depression. Pharmacogenomics J 2002; 2(3): 191–6PubMedCrossRef Roberts RL, Joyce PR, Mulder RT, et al. A common P-glycoprotein polymorphism is associated with nortriptyline-induced postural hypotension in patients treated for major depression. Pharmacogenomics J 2002; 2(3): 191–6PubMedCrossRef
265.
Zurück zum Zitat Sun J, He ZG, Cheng G, et al. Multidrug resistance P-glycoprotein: crucial significance in drug disposition and interaction. Med Sci Monit 2004; 10(1): RA5–14PubMed Sun J, He ZG, Cheng G, et al. Multidrug resistance P-glycoprotein: crucial significance in drug disposition and interaction. Med Sci Monit 2004; 10(1): RA5–14PubMed
266.
Zurück zum Zitat DuBuske LM. The role of P-glycoprotein and organic anion-transporting polypeptides in drug interactions. Drug Saf 2005; 28(9): 789–801PubMedCrossRef DuBuske LM. The role of P-glycoprotein and organic anion-transporting polypeptides in drug interactions. Drug Saf 2005; 28(9): 789–801PubMedCrossRef
267.
Zurück zum Zitat Brinkmann U, Eichelbaum M. Polymorphisms in the ABC drug transporter gene MDR1. Pharmacogenomics J 2001; 1(1): 59–64PubMedCrossRef Brinkmann U, Eichelbaum M. Polymorphisms in the ABC drug transporter gene MDR1. Pharmacogenomics J 2001; 1(1): 59–64PubMedCrossRef
268.
Zurück zum Zitat Brinkmann U, Roots I, Eichelbaum M. Pharmacogenetics of the human drug-transporter gene MDR1: impact of polymorphisms on pharmacotherapy. Drug Discov Today 2001; 6(16): 835–9PubMedCrossRef Brinkmann U, Roots I, Eichelbaum M. Pharmacogenetics of the human drug-transporter gene MDR1: impact of polymorphisms on pharmacotherapy. Drug Discov Today 2001; 6(16): 835–9PubMedCrossRef
269.
Zurück zum Zitat Kerb R, Hoffmeyer S, Brinkmann U. ABC drug transporters: hereditary polymorphisms and pharmacological impact in MDR1, MRP1 and MRP2. Pharmacogenomics 2001; 2(1): 51–64PubMedCrossRef Kerb R, Hoffmeyer S, Brinkmann U. ABC drug transporters: hereditary polymorphisms and pharmacological impact in MDR1, MRP1 and MRP2. Pharmacogenomics 2001; 2(1): 51–64PubMedCrossRef
270.
Zurück zum Zitat Sakaeda T, Nakamura T, Okumura K. MDR1 genotype-related pharmacokinetics and pharmacodynamics. Biol Pharm Bull 2002; 25(11): 1391–400PubMedCrossRef Sakaeda T, Nakamura T, Okumura K. MDR1 genotype-related pharmacokinetics and pharmacodynamics. Biol Pharm Bull 2002; 25(11): 1391–400PubMedCrossRef
271.
Zurück zum Zitat Hoffmeyer S, Burk O, von Richter O, et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci U S A 2000; 97(7): 3473–8PubMedCrossRef Hoffmeyer S, Burk O, von Richter O, et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci U S A 2000; 97(7): 3473–8PubMedCrossRef
272.
Zurück zum Zitat Sadeque AJ, Wandel C, He H, et al. Increased drug delivery to the brain by P-glycoprotein inhibition. Clin Pharmacol Ther 2000; 68(3): 231–7PubMedCrossRef Sadeque AJ, Wandel C, He H, et al. Increased drug delivery to the brain by P-glycoprotein inhibition. Clin Pharmacol Ther 2000; 68(3): 231–7PubMedCrossRef
273.
Zurück zum Zitat Perry PJ, Pfohl BM, Holstad SG. The relationship between antidepressant response and tricyclic antidepressant plasma concentrations: a retrospective analysis of the literature using logistic regression analysis. Clin Pharmacokinet 1987; 13(6): 381–92PubMedCrossRef Perry PJ, Pfohl BM, Holstad SG. The relationship between antidepressant response and tricyclic antidepressant plasma concentrations: a retrospective analysis of the literature using logistic regression analysis. Clin Pharmacokinet 1987; 13(6): 381–92PubMedCrossRef
274.
Zurück zum Zitat Perry PJ, Zeilmann C, Arndt S. Tricyclic antidepressant concentrations in plasma: an estimate of their sensitivity and specificity as a predictor of response. J Clin Psychopharmacol 1994; 14(4): 230–40PubMedCrossRef Perry PJ, Zeilmann C, Arndt S. Tricyclic antidepressant concentrations in plasma: an estimate of their sensitivity and specificity as a predictor of response. J Clin Psychopharmacol 1994; 14(4): 230–40PubMedCrossRef
275.
Zurück zum Zitat Ulrich S, Neuhof S, Braun V, et al. Therapeutic window of serum haloperidol concentration in acute schizophrenia and schizoaffective disorder. Pharmacopsychiatry 1998; 31(5): 163–9PubMedCrossRef Ulrich S, Neuhof S, Braun V, et al. Therapeutic window of serum haloperidol concentration in acute schizophrenia and schizoaffective disorder. Pharmacopsychiatry 1998; 31(5): 163–9PubMedCrossRef
276.
Zurück zum Zitat Ulrich S, Lauter J. Comprehensive survey of the relationship between serum concentration and therapeutic effect of amitriptyline in depression. Clin Pharmacokinet 2002; 41(11): 853–76PubMedCrossRef Ulrich S, Lauter J. Comprehensive survey of the relationship between serum concentration and therapeutic effect of amitriptyline in depression. Clin Pharmacokinet 2002; 41(11): 853–76PubMedCrossRef
277.
Zurück zum Zitat Ulrich S, Wurthmann C, Brosz M, et al. The relationship between serum concentration and therapeutic effect of haloperidol in patients with acute schizophrenia. Clin Pharmacokinet 1998; 34(3): 227–63PubMedCrossRef Ulrich S, Wurthmann C, Brosz M, et al. The relationship between serum concentration and therapeutic effect of haloperidol in patients with acute schizophrenia. Clin Pharmacokinet 1998; 34(3): 227–63PubMedCrossRef
278.
Zurück zum Zitat Gex-Fabry M, Balant-Gorgia AE, Balant LP. Clomipramine concentration as a predictor of delayed response: a naturalistic study. Eur J Clin Pharmacol 1999; 54(12): 895–902PubMedCrossRef Gex-Fabry M, Balant-Gorgia AE, Balant LP. Clomipramine concentration as a predictor of delayed response: a naturalistic study. Eur J Clin Pharmacol 1999; 54(12): 895–902PubMedCrossRef
279.
Zurück zum Zitat Eilers R. Therapeutic drug monitoring for the treatment of psychiatric disorders: clinical use and cost effectiveness. Clin Pharmacokinet 1995; 29(6): 442–50PubMedCrossRef Eilers R. Therapeutic drug monitoring for the treatment of psychiatric disorders: clinical use and cost effectiveness. Clin Pharmacokinet 1995; 29(6): 442–50PubMedCrossRef
280.
Zurück zum Zitat Balant-Gorgia AE, Gex-Fabry M, Balant LP. Clinical pharmacokinetics of clomipramine. Clin Pharmacokinet 1991; 20(6): 447–62PubMedCrossRef Balant-Gorgia AE, Gex-Fabry M, Balant LP. Clinical pharmacokinetics of clomipramine. Clin Pharmacokinet 1991; 20(6): 447–62PubMedCrossRef
281.
Zurück zum Zitat Baldessarini RJ, Cohen BM, Teicher MH. Significance of neuroleptic dose and plasma level in the pharmacological treatment of psychoses. Arch Gen Psychiatry 1988; 45(1): 79–91PubMedCrossRef Baldessarini RJ, Cohen BM, Teicher MH. Significance of neuroleptic dose and plasma level in the pharmacological treatment of psychoses. Arch Gen Psychiatry 1988; 45(1): 79–91PubMedCrossRef
282.
Zurück zum Zitat Rao ML, Hiemke C, Grasmader K, et al. [Olanzapine: pharmacology, pharmacokinetics and therapeutic drug monitoring]. Fortschr Neurol Psychiatr 2001; 69(11): 510–7PubMedCrossRef Rao ML, Hiemke C, Grasmader K, et al. [Olanzapine: pharmacology, pharmacokinetics and therapeutic drug monitoring]. Fortschr Neurol Psychiatr 2001; 69(11): 510–7PubMedCrossRef
283.
Zurück zum Zitat Hiemke C, Dragicevic A, Grander G. Therapeutic monitoring of new antipsychotic drugs. Ther Drug Monit 2004; 26(2): 156–60PubMedCrossRef Hiemke C, Dragicevic A, Grander G. Therapeutic monitoring of new antipsychotic drugs. Ther Drug Monit 2004; 26(2): 156–60PubMedCrossRef
284.
Zurück zum Zitat Asberg M, Sjoqvist F. On the role of plasma level monitoring of tricyclic antidepressants in clinical practice. Commun Psychopharmacol 1978; 2(5): 381–91PubMed Asberg M, Sjoqvist F. On the role of plasma level monitoring of tricyclic antidepressants in clinical practice. Commun Psychopharmacol 1978; 2(5): 381–91PubMed
285.
Zurück zum Zitat de Oliveira IR, Dardennes RM, Amorim ES, et al. Is there a relationship between antipsychotic blood levels and their clinical efficacy? An analysis of studies design and methodology. Fundam Clin Pharmacol 1995; 9(5): 488–502PubMedCrossRef de Oliveira IR, Dardennes RM, Amorim ES, et al. Is there a relationship between antipsychotic blood levels and their clinical efficacy? An analysis of studies design and methodology. Fundam Clin Pharmacol 1995; 9(5): 488–502PubMedCrossRef
286.
Zurück zum Zitat Gram LF. Plasma level monitoring of tricyclic antidepressants: methodological and pharmacokinetic considerations. Commun Psychopharmacol 1978; 2(5): 373–80PubMed Gram LF. Plasma level monitoring of tricyclic antidepressants: methodological and pharmacokinetic considerations. Commun Psychopharmacol 1978; 2(5): 373–80PubMed
287.
Zurück zum Zitat Preskorn SH, Burke MJ, Fast GA. Therapeutic drug monitoring: principles and practice. Psychiatr Clin North Am 1993; 16(3): 611–45PubMed Preskorn SH, Burke MJ, Fast GA. Therapeutic drug monitoring: principles and practice. Psychiatr Clin North Am 1993; 16(3): 611–45PubMed
288.
Zurück zum Zitat Van Putten T, Marder SR. Variable dose studies provide misleading therapeutic windows. J Clin Psychopharmacol 1986; 6(4): 249–50PubMed Van Putten T, Marder SR. Variable dose studies provide misleading therapeutic windows. J Clin Psychopharmacol 1986; 6(4): 249–50PubMed
289.
Zurück zum Zitat Task Force on the Use of Laboratory Tests in Psychiatry. Tricyclic antidepressants: blood level measurements and clinical outcome: an APA Task Force report. Am J Psychiatry 1985; 142 (2): 155–62 Task Force on the Use of Laboratory Tests in Psychiatry. Tricyclic antidepressants: blood level measurements and clinical outcome: an APA Task Force report. Am J Psychiatry 1985; 142 (2): 155–62
290.
Zurück zum Zitat Nyberg S, Nordstrom AL, Halldin C, et al. Positron emission tomography studies on D2 dopamine receptor occupancy and plasma antipsychotic drug levels in man. Int Clin Psychopharmacol 1995; 10Suppl. 3: 81–5PubMed Nyberg S, Nordstrom AL, Halldin C, et al. Positron emission tomography studies on D2 dopamine receptor occupancy and plasma antipsychotic drug levels in man. Int Clin Psychopharmacol 1995; 10Suppl. 3: 81–5PubMed
291.
Zurück zum Zitat Sedvall G, Farde L, Hall H, et al. Utilization of radioligands in schizophrenia research. Clin Neurosci 1995; 3(2): 112–21PubMed Sedvall G, Farde L, Hall H, et al. Utilization of radioligands in schizophrenia research. Clin Neurosci 1995; 3(2): 112–21PubMed
292.
Zurück zum Zitat Rasmussen BB, Brosen K. Is therapeutic drug monitoring a case for optimizing clinical outcome and avoiding interactions of the selective serotonin reuptake inhibitors? Ther Drug Monit 2000; 22(2): 143–54PubMedCrossRef Rasmussen BB, Brosen K. Is therapeutic drug monitoring a case for optimizing clinical outcome and avoiding interactions of the selective serotonin reuptake inhibitors? Ther Drug Monit 2000; 22(2): 143–54PubMedCrossRef
293.
Zurück zum Zitat Hammer WM, Brodiet BB. Application of isotope derivative technique to assay of secondary amines: estimation of desipramine by acetylation with H3-acetic anhydride. J Pharmacol Exp Ther 1967; 157(3): 503–8PubMed Hammer WM, Brodiet BB. Application of isotope derivative technique to assay of secondary amines: estimation of desipramine by acetylation with H3-acetic anhydride. J Pharmacol Exp Ther 1967; 157(3): 503–8PubMed
294.
Zurück zum Zitat Asberg M, Cronholm B, Sjoqvist F, et al. Relationship between plasma level and therapeutic effect of nortriptyline. BMJ 1971; 3(770): 331–4PubMedCrossRef Asberg M, Cronholm B, Sjoqvist F, et al. Relationship between plasma level and therapeutic effect of nortriptyline. BMJ 1971; 3(770): 331–4PubMedCrossRef
295.
Zurück zum Zitat Mitchell PB. Therapeutic drug monitoring of psychotropic medications. Br J Clin Pharmacol 2001; 52: 45S–54SPubMedCrossRef Mitchell PB. Therapeutic drug monitoring of psychotropic medications. Br J Clin Pharmacol 2001; 52: 45S–54SPubMedCrossRef
296.
Zurück zum Zitat Bengtsson F. Therapeutic drug monitoring of psychotropic drugs. TDM “nouveau”. Ther Drug Monit 2004; 26(2): 145–51PubMedCrossRef Bengtsson F. Therapeutic drug monitoring of psychotropic drugs. TDM “nouveau”. Ther Drug Monit 2004; 26(2): 145–51PubMedCrossRef
297.
Zurück zum Zitat Vuille F, Amey M, Baumann P. Use of plasma level monitoring of antidepressants in clinical practice: towards an analysis of clinical utility. Pharmacopsychiatry 1991; 24(6): 190–5PubMedCrossRef Vuille F, Amey M, Baumann P. Use of plasma level monitoring of antidepressants in clinical practice: towards an analysis of clinical utility. Pharmacopsychiatry 1991; 24(6): 190–5PubMedCrossRef
298.
Zurück zum Zitat Gefvert O, Eriksson B, Persson P, et al. Pharmacokinetics and D2 receptor occupancy of long-acting injectable risperidone (risperdal consta) in patients with schizophrenia. Int J Neuropsychopharmacol 2005; 8(1): 27–36PubMedCrossRef Gefvert O, Eriksson B, Persson P, et al. Pharmacokinetics and D2 receptor occupancy of long-acting injectable risperidone (risperdal consta) in patients with schizophrenia. Int J Neuropsychopharmacol 2005; 8(1): 27–36PubMedCrossRef
299.
Zurück zum Zitat Peloquin CA. Therapeutic drug monitoring in the treatment of tuberculosis. Drugs 2002; 62(15): 2169–83PubMedCrossRef Peloquin CA. Therapeutic drug monitoring in the treatment of tuberculosis. Drugs 2002; 62(15): 2169–83PubMedCrossRef
300.
Zurück zum Zitat Heller S, Hiemke C, Stroba G, et al. Assessment of storage and transport stability of new antidepressant and antipsychotic drugs for a nationwide TDM service. Ther Drug Monit 2004; 26(4): 459–61PubMedCrossRef Heller S, Hiemke C, Stroba G, et al. Assessment of storage and transport stability of new antidepressant and antipsychotic drugs for a nationwide TDM service. Ther Drug Monit 2004; 26(4): 459–61PubMedCrossRef
301.
Zurück zum Zitat Morris RG, Holt DW, Armstrong VW, et al. Analytic aspects of cyclosporine monitoring, on behalf of the IFCC/IATDMCT Joint Working Group. Ther Drug Monit 2004; 26(2): 227–30PubMedCrossRef Morris RG, Holt DW, Armstrong VW, et al. Analytic aspects of cyclosporine monitoring, on behalf of the IFCC/IATDMCT Joint Working Group. Ther Drug Monit 2004; 26(2): 227–30PubMedCrossRef
302.
Zurück zum Zitat Jusko WJ, Thomson AW, Fung J, et al. Consensus document: therapeutic monitoring of tacrolimus (FK-506). Ther Drug Monit 1995; 17(6): 606–14PubMedCrossRef Jusko WJ, Thomson AW, Fung J, et al. Consensus document: therapeutic monitoring of tacrolimus (FK-506). Ther Drug Monit 1995; 17(6): 606–14PubMedCrossRef
303.
Zurück zum Zitat Shaw LM, Sollinger HW, Halloran P, et al. Mycophenolate mofetil: a report of the consensus panel. Ther Drug Monit 1995; 17(6): 690–9PubMedCrossRef Shaw LM, Sollinger HW, Halloran P, et al. Mycophenolate mofetil: a report of the consensus panel. Ther Drug Monit 1995; 17(6): 690–9PubMedCrossRef
304.
Zurück zum Zitat Yatscoff RW, Boeckx R, Holt DW, et al. Consensus guidelines for therapeutic drug monitoring of rapamycin: report of the consensus panel. Ther Drug Monit 1995; 17(6): 676–80PubMedCrossRef Yatscoff RW, Boeckx R, Holt DW, et al. Consensus guidelines for therapeutic drug monitoring of rapamycin: report of the consensus panel. Ther Drug Monit 1995; 17(6): 676–80PubMedCrossRef
305.
Zurück zum Zitat Kappelhoff BS, Crommentuyn KM, de Maat MM, et al. Practical guidelines to interpret plasma concentrations of antiretroviral drugs. Clin Pharmacokinet 2004; 43(13): 845–53PubMedCrossRef Kappelhoff BS, Crommentuyn KM, de Maat MM, et al. Practical guidelines to interpret plasma concentrations of antiretroviral drugs. Clin Pharmacokinet 2004; 43(13): 845–53PubMedCrossRef
306.
Zurück zum Zitat Acosta EP, Gerber JG. Position paper on therapeutic drug monitoring of antiretroviral agents. AIDS Res Hum Retroviruses 2002; 18(12): 825–34PubMedCrossRef Acosta EP, Gerber JG. Position paper on therapeutic drug monitoring of antiretroviral agents. AIDS Res Hum Retroviruses 2002; 18(12): 825–34PubMedCrossRef
307.
308.
Zurück zum Zitat Regenthal R, Krueger M, Koeppel C, et al. Drug levels: therapeutic and toxic serum/plasma concentrations of common drugs. J Clin Monit Comput 1999; 15(7-8): 529–44PubMedCrossRef Regenthal R, Krueger M, Koeppel C, et al. Drug levels: therapeutic and toxic serum/plasma concentrations of common drugs. J Clin Monit Comput 1999; 15(7-8): 529–44PubMedCrossRef
309.
Zurück zum Zitat Schulz M, Schmoldt A. Therapeutic and toxic blood concentrations of more than 800 drugs and other xenobiotics. Pharmazie 2003; 58(7): 447–74PubMed Schulz M, Schmoldt A. Therapeutic and toxic blood concentrations of more than 800 drugs and other xenobiotics. Pharmazie 2003; 58(7): 447–74PubMed
310.
Zurück zum Zitat Ensom MH, Chang TK, Patel P. Pharmacogenetics: the therapeutic drug monitoring of the future? Clin Pharmacokinet 2001; 40(11): 783–802PubMedCrossRef Ensom MH, Chang TK, Patel P. Pharmacogenetics: the therapeutic drug monitoring of the future? Clin Pharmacokinet 2001; 40(11): 783–802PubMedCrossRef
311.
Zurück zum Zitat Chainuvati S, Nafziger AN, Leeder JS, et al. Combined phenotypic assessment of cytochrome p450 1A2, 2C9, 2C19, 2D6, and 3A, N-acetyltransferase-2, and xanthine oxidase activities with the “Cooperstown 5+1 cocktail”. Clin Pharmacol Ther 2003; 74(5): 437–47PubMedCrossRef Chainuvati S, Nafziger AN, Leeder JS, et al. Combined phenotypic assessment of cytochrome p450 1A2, 2C9, 2C19, 2D6, and 3A, N-acetyltransferase-2, and xanthine oxidase activities with the “Cooperstown 5+1 cocktail”. Clin Pharmacol Ther 2003; 74(5): 437–47PubMedCrossRef
312.
Zurück zum Zitat Jerdi MC, Daali Y, Oestreicher MK, et al. A simplified analytical method for a phenotyping cocktail of major CYP450 biotransformation routes. J Pharm Biomed Anal 2004; 35(5): 1203–12PubMedCrossRef Jerdi MC, Daali Y, Oestreicher MK, et al. A simplified analytical method for a phenotyping cocktail of major CYP450 biotransformation routes. J Pharm Biomed Anal 2004; 35(5): 1203–12PubMedCrossRef
313.
Zurück zum Zitat Streetman DS, Bleakley JF, Kim JS, et al. Combined phenotypic assessment of CYP1A2, CYP2C19, CYP2D6, CYP3A, Nacetyltransferase-2, and xanthine oxidase with the “Cooperstown cocktail”. Clin Pharmacol Ther 2000; 68(4): 375–83PubMedCrossRef Streetman DS, Bleakley JF, Kim JS, et al. Combined phenotypic assessment of CYP1A2, CYP2C19, CYP2D6, CYP3A, Nacetyltransferase-2, and xanthine oxidase with the “Cooperstown cocktail”. Clin Pharmacol Ther 2000; 68(4): 375–83PubMedCrossRef
314.
Zurück zum Zitat Dahl ML. Cytochrome p450 phenotyping/genotyping in patients receiving antipsychotics: useful aid to prescribing? Clin Pharmacokinet 2002; 41(7): 453–70PubMedCrossRef Dahl ML. Cytochrome p450 phenotyping/genotyping in patients receiving antipsychotics: useful aid to prescribing? Clin Pharmacokinet 2002; 41(7): 453–70PubMedCrossRef
315.
Zurück zum Zitat Schubert L. Ethical implications of pharmacogenetics - do slippery slope arguments matter? Bioethics 2004; 18(4): 361–78PubMedCrossRef Schubert L. Ethical implications of pharmacogenetics - do slippery slope arguments matter? Bioethics 2004; 18(4): 361–78PubMedCrossRef
316.
Zurück zum Zitat Netzer C, Biller-Andorno N. Pharmacogenetic testing, informed consent and the problem of secondary information. Bioethics 2004; 18(4): 344–60PubMedCrossRef Netzer C, Biller-Andorno N. Pharmacogenetic testing, informed consent and the problem of secondary information. Bioethics 2004; 18(4): 344–60PubMedCrossRef
317.
Zurück zum Zitat Smart A, Martin P, Parker M. Tailored medicine: whom will it fit? The ethics of patient and disease stratification. Bioethics 2004; 18(4): 322–42PubMedCrossRef Smart A, Martin P, Parker M. Tailored medicine: whom will it fit? The ethics of patient and disease stratification. Bioethics 2004; 18(4): 322–42PubMedCrossRef
318.
Zurück zum Zitat van Delden J, Bolt I, Kalis A, et al. Tailor-made pharmacotherapy: future developments and ethical challenges in the field of pharmacogenomics. Bioethics 2004; 18(4): 303–21PubMedCrossRef van Delden J, Bolt I, Kalis A, et al. Tailor-made pharmacotherapy: future developments and ethical challenges in the field of pharmacogenomics. Bioethics 2004; 18(4): 303–21PubMedCrossRef
319.
Zurück zum Zitat Paul NW, Roses AD. Pharmacogenetics and pharmacogenomics: recent developments, their clinical relevance and some ethical, social, and legal implications. J Mol Med 2003; 81(3): 135–40 Paul NW, Roses AD. Pharmacogenetics and pharmacogenomics: recent developments, their clinical relevance and some ethical, social, and legal implications. J Mol Med 2003; 81(3): 135–40
320.
Zurück zum Zitat de Leon J, Barnhill J, Rogers T, et al. Pilot study of the cytochrome P450-2D6 genotype in a psychiatric state hospital. Am J Psychiatry 1998; 155(9): 1278–80PubMed de Leon J, Barnhill J, Rogers T, et al. Pilot study of the cytochrome P450-2D6 genotype in a psychiatric state hospital. Am J Psychiatry 1998; 155(9): 1278–80PubMed
321.
Zurück zum Zitat Chou WH, Yan FX, de Leon J, et al. Extension of a pilot study: impact from the cytochrome P450 2D6 polymorphism on outcome and costs associated with severe mental illness. J Clin Psychopharmacol 2000; 20(2): 246–51PubMedCrossRef Chou WH, Yan FX, de Leon J, et al. Extension of a pilot study: impact from the cytochrome P450 2D6 polymorphism on outcome and costs associated with severe mental illness. J Clin Psychopharmacol 2000; 20(2): 246–51PubMedCrossRef
322.
Zurück zum Zitat Rau T, Wohlleben G, Wuttke H, et al. CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study. Clin Pharmacol Ther 2004; 75(5): 386–93PubMedCrossRef Rau T, Wohlleben G, Wuttke H, et al. CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study. Clin Pharmacol Ther 2004; 75(5): 386–93PubMedCrossRef
323.
Zurück zum Zitat Tamminga WJ, Wemer J, Oosterhuis B, et al. Polymorphic drug metabolism (CYP2D6) and utilisation of psychotropic drugs in hospitalised psychiatric patients: a retrospective study. Eur J Clin Pharmacol 2003; 59(1): 57–64PubMed Tamminga WJ, Wemer J, Oosterhuis B, et al. Polymorphic drug metabolism (CYP2D6) and utilisation of psychotropic drugs in hospitalised psychiatric patients: a retrospective study. Eur J Clin Pharmacol 2003; 59(1): 57–64PubMed
324.
Zurück zum Zitat Mulder H, Wilmink FW, Beumer TL, et al. The association between cytochrome P450 2D6 genotype and prescription patterns of antipsychotic and antidepressant drugs in hospitalized psychiatric patients: a retrospective follow-up study. J Clin Psychopharmacol 2005; 25(2): 188–91PubMedCrossRef Mulder H, Wilmink FW, Beumer TL, et al. The association between cytochrome P450 2D6 genotype and prescription patterns of antipsychotic and antidepressant drugs in hospitalized psychiatric patients: a retrospective follow-up study. J Clin Psychopharmacol 2005; 25(2): 188–91PubMedCrossRef
325.
Zurück zum Zitat de Leon J, Susce MT, Pan RM, et al. The CYP2D6 poor metabolizer phenotype may be associated with risperidone adverse drug reactions and discontinuation. J Clin Psychiatry 2005; 66(1): 15–27PubMedCrossRef de Leon J, Susce MT, Pan RM, et al. The CYP2D6 poor metabolizer phenotype may be associated with risperidone adverse drug reactions and discontinuation. J Clin Psychiatry 2005; 66(1): 15–27PubMedCrossRef
326.
Zurück zum Zitat Brockmöller J, Kirchheiner J, Schmider J, et al. The impact of the CYP2D6 polymorphism on haloperidol pharmacokinetics and on the outcome of haloperidol treatment. Clin Pharmacol Ther 2002; 72(4): 438–52PubMedCrossRef Brockmöller J, Kirchheiner J, Schmider J, et al. The impact of the CYP2D6 polymorphism on haloperidol pharmacokinetics and on the outcome of haloperidol treatment. Clin Pharmacol Ther 2002; 72(4): 438–52PubMedCrossRef
327.
Zurück zum Zitat de Leon J, Susce MT, Pan RM, et al. Polymorphic variations in GSTM1, GSTT1, PgP, CYP2D6, CYP3A5, and dopamine D2 and D3 receptors and their association with tardive dyskinesia in severe mental illness. J Clin Psychopharmacol 2005; 25 (5): 448–56CrossRef de Leon J, Susce MT, Pan RM, et al. Polymorphic variations in GSTM1, GSTT1, PgP, CYP2D6, CYP3A5, and dopamine D2 and D3 receptors and their association with tardive dyskinesia in severe mental illness. J Clin Psychopharmacol 2005; 25 (5): 448–56CrossRef
328.
Zurück zum Zitat Armstrong M, Daly AK, Blennerhassett R, et al. Antipsychotic drug-induced movement disorders in schizophrenics in relation to CYP2D6 genotype. Br J Psychiatry 1997; 170: 23–6PubMedCrossRef Armstrong M, Daly AK, Blennerhassett R, et al. Antipsychotic drug-induced movement disorders in schizophrenics in relation to CYP2D6 genotype. Br J Psychiatry 1997; 170: 23–6PubMedCrossRef
329.
Zurück zum Zitat Reggiani K, Vandel P, Haffen E, et al. Effets indesirables extrapyramidaux des neuroleptiques et antidepresseurs: recherche de facteurs de risque: role du polymorphisme genetique du CYP2D6. L’Encephale 2000; 26(1): 62–7PubMed Reggiani K, Vandel P, Haffen E, et al. Effets indesirables extrapyramidaux des neuroleptiques et antidepresseurs: recherche de facteurs de risque: role du polymorphisme genetique du CYP2D6. L’Encephale 2000; 26(1): 62–7PubMed
330.
Zurück zum Zitat Steimer W, Zopf K, von Amelunxen S, et al. Amitriptyline or not, that is the question: pharmacogenetic testing of CYP2D6 and CYP2C19 identifies patients with low or high risk for side effects in amitriptyline therapy. Clin Chem 2005; 51(2): 376–85PubMedCrossRef Steimer W, Zopf K, von Amelunxen S, et al. Amitriptyline or not, that is the question: pharmacogenetic testing of CYP2D6 and CYP2C19 identifies patients with low or high risk for side effects in amitriptyline therapy. Clin Chem 2005; 51(2): 376–85PubMedCrossRef
331.
Zurück zum Zitat Grasmader K, Verwohlt PL, Rietschel M, et al. Impact of polymorphisms of cytochrome-P450 isoenzymes 2C9, 2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting. Eur J Clin Pharmacol 2004; 60(5): 329–36PubMedCrossRef Grasmader K, Verwohlt PL, Rietschel M, et al. Impact of polymorphisms of cytochrome-P450 isoenzymes 2C9, 2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting. Eur J Clin Pharmacol 2004; 60(5): 329–36PubMedCrossRef
332.
Zurück zum Zitat Rau T, Heide R, Bergmann K, et al. Effect of the CYP2D6 genotype on metoprolol metabolism persists during long-term treatment. Pharmacogenetics 2002; 12(6): 465–72PubMedCrossRef Rau T, Heide R, Bergmann K, et al. Effect of the CYP2D6 genotype on metoprolol metabolism persists during long-term treatment. Pharmacogenetics 2002; 12(6): 465–72PubMedCrossRef
333.
Zurück zum Zitat Wuttke H, Rau T, Heide R, et al. Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects. Clin Pharmacol Ther 2002; 72(4): 429–37PubMedCrossRef Wuttke H, Rau T, Heide R, et al. Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects. Clin Pharmacol Ther 2002; 72(4): 429–37PubMedCrossRef
334.
Zurück zum Zitat Basile VS, Ozdemir V, Masellis M, et al. A functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene: association with tardive dyskinesia in schizophrenia. Mol Psychiatry 2000; 5(4): 410–7PubMedCrossRef Basile VS, Ozdemir V, Masellis M, et al. A functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene: association with tardive dyskinesia in schizophrenia. Mol Psychiatry 2000; 5(4): 410–7PubMedCrossRef
335.
Zurück zum Zitat Tiwari AK, Deshpande SN, Rao AR, et al. Genetic susceptibility to tardive dyskinesia in chronic schizophrenia subjects: I. Association of CYP1A2 gene polymorphism. Pharmacogenomics J 2005; 5(1): 60–9PubMedCrossRef Tiwari AK, Deshpande SN, Rao AR, et al. Genetic susceptibility to tardive dyskinesia in chronic schizophrenia subjects: I. Association of CYP1A2 gene polymorphism. Pharmacogenomics J 2005; 5(1): 60–9PubMedCrossRef
336.
Zurück zum Zitat Lerer B, Segman RH, Fangerau H, et al. Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism. Neuropsychopharmacology 2002; 27(1): 105–19PubMedCrossRef Lerer B, Segman RH, Fangerau H, et al. Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism. Neuropsychopharmacology 2002; 27(1): 105–19PubMedCrossRef
337.
Zurück zum Zitat Ozdemir V, Basile VS, Masellis M, et al. Pharmacogenetic assessment of antipsychotic-induced movement disorders: contribution of the dopamine D3 receptor and cytochrome P450 1A2 genes. J Biochem Biophys Methods 2001; 47(1-2): 151–7PubMedCrossRef Ozdemir V, Basile VS, Masellis M, et al. Pharmacogenetic assessment of antipsychotic-induced movement disorders: contribution of the dopamine D3 receptor and cytochrome P450 1A2 genes. J Biochem Biophys Methods 2001; 47(1-2): 151–7PubMedCrossRef
338.
Zurück zum Zitat Taube J, Halsall D, Baglin T. Influence of cytochrome P450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment. Blood 2000; 96(5): 1816–9PubMed Taube J, Halsall D, Baglin T. Influence of cytochrome P450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment. Blood 2000; 96(5): 1816–9PubMed
339.
Zurück zum Zitat Wilke RA, Carrillo MW, Ritchie MD. Pacific symposium on biocomputing: computational approaches for pharmacogenomics. Pharmacogenomics 2005; 6(2): 111–3PubMedCrossRef Wilke RA, Carrillo MW, Ritchie MD. Pacific symposium on biocomputing: computational approaches for pharmacogenomics. Pharmacogenomics 2005; 6(2): 111–3PubMedCrossRef
340.
Zurück zum Zitat Ingelman-Sundberg M. Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity. Pharmacogenomics J 2005; 5(1): 6–13PubMedCrossRef Ingelman-Sundberg M. Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity. Pharmacogenomics J 2005; 5(1): 6–13PubMedCrossRef
341.
Zurück zum Zitat Veenstra DL, Higashi MK, Phillips KA. Assessing the cost-effectiveness of pharmacogenomics. AAPS PharmSci 2000; 2(3): E29PubMedCrossRef Veenstra DL, Higashi MK, Phillips KA. Assessing the cost-effectiveness of pharmacogenomics. AAPS PharmSci 2000; 2(3): E29PubMedCrossRef
342.
Zurück zum Zitat Simmons SA, Perry PJ, Rickert ED, et al. Cost-benefit analysis of prospective pharmacokinetic dosing of nortriptyline in depressed inpatients. J Affect Disord 1985; 8(1): 47–53PubMedCrossRef Simmons SA, Perry PJ, Rickert ED, et al. Cost-benefit analysis of prospective pharmacokinetic dosing of nortriptyline in depressed inpatients. J Affect Disord 1985; 8(1): 47–53PubMedCrossRef
343.
Zurück zum Zitat Preskorn SH, Fast GA. Therapeutic drug monitoring for antidepressants: efficacy, safety, and cost effectiveness. J Clin Psychiatry 1991; 52Suppl.: 23–33PubMed Preskorn SH, Fast GA. Therapeutic drug monitoring for antidepressants: efficacy, safety, and cost effectiveness. J Clin Psychiatry 1991; 52Suppl.: 23–33PubMed
344.
Zurück zum Zitat Lundmark J, Bengtsson F, Nordin C, et al. Therapeutic drug monitoring of selective serotonin reuptake inhibitors influences clinical dosing strategies and reduces drug costs in depressed elderly patients. Acta Psychiatr Scand 2000; 101 (5): 354–9CrossRef Lundmark J, Bengtsson F, Nordin C, et al. Therapeutic drug monitoring of selective serotonin reuptake inhibitors influences clinical dosing strategies and reduces drug costs in depressed elderly patients. Acta Psychiatr Scand 2000; 101 (5): 354–9CrossRef
345.
Zurück zum Zitat Muller MJ, Dragicevic A, Fric M, et al. Therapeutic drug monitoring of tricyclic antidepressants: how does it work under clinical conditions? Pharmacopsychiatry 2003; 36(3): 98–104PubMedCrossRef Muller MJ, Dragicevic A, Fric M, et al. Therapeutic drug monitoring of tricyclic antidepressants: how does it work under clinical conditions? Pharmacopsychiatry 2003; 36(3): 98–104PubMedCrossRef
346.
Zurück zum Zitat Chen S, Chou WH, Blouin RA, et al. The cytochrome P450 2D6 (CYP2D6) enzyme polymorphism: screening costs and influence on clinical outcomes in psychiatry. Clin Pharmacol Ther 1996; 60(5): 522–34PubMedCrossRef Chen S, Chou WH, Blouin RA, et al. The cytochrome P450 2D6 (CYP2D6) enzyme polymorphism: screening costs and influence on clinical outcomes in psychiatry. Clin Pharmacol Ther 1996; 60(5): 522–34PubMedCrossRef
347.
Zurück zum Zitat Frueh FW, Gurwitz D. From pharmacogenetics to personalized medicine: a vital need for educating health professionals and the community. Pharmacogenomics 2004; 5(5): 571–9PubMedCrossRef Frueh FW, Gurwitz D. From pharmacogenetics to personalized medicine: a vital need for educating health professionals and the community. Pharmacogenomics 2004; 5(5): 571–9PubMedCrossRef
348.
Zurück zum Zitat Hug H, Bagatto D, Dannecker R, et al. ADRIS: the adverse drug reactions information scheme. Pharmacogenetics 2003; 13(12): 767–72PubMedCrossRef Hug H, Bagatto D, Dannecker R, et al. ADRIS: the adverse drug reactions information scheme. Pharmacogenetics 2003; 13(12): 767–72PubMedCrossRef
Metadaten
Titel
Therapeutic Drug Monitoring and Pharmacogenetic Tests as Tools in Pharmacovigilance
verfasst von
Eveline Jaquenoud Sirot
Jan Willem van der Velden
Katharina Rentsch
Chin B. Eap
Pierre Baumann
Publikationsdatum
01.09.2006
Verlag
Springer International Publishing
Erschienen in
Drug Safety / Ausgabe 9/2006
Print ISSN: 0114-5916
Elektronische ISSN: 1179-1942
DOI
https://doi.org/10.2165/00002018-200629090-00001

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