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Erschienen in: Clinical Pharmacokinetics 3/2015

01.03.2015 | Letter to the Editor

Quantitative Methods for Prediction of the Effect of Cytochrome P450 Gene Polymorphisms on Substrate Drug Exposure

verfasst von: Sylvain Goutelle, Michel Tod

Erschienen in: Clinical Pharmacokinetics | Ausgabe 3/2015

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Excerpt

We read with interest the article by Chang and colleagues who studied the influence of cytochrome P450 2C19 (CYP2C19) genetic polymorphism on citalopram and escitalopram exposure by using meta-analysis [1]. The authors state that this is the first study which provides precise estimates of the influence of CYP2C19 genotypes on (es)citalopram drug exposure, especially for heterozygous genotypes with the CYP2C19*17 gain-of-function allele. …
Literatur
1.
Zurück zum Zitat Chang M, Tybring G, Dahl ML, Lindh JD. Impact of cytochrome P450 2C19 polymorphisms on citalopram/escitalopram exposure: a systematic review and meta-analysis. Clin Pharmacokinet. 2014;53(9):801–11.CrossRefPubMed Chang M, Tybring G, Dahl ML, Lindh JD. Impact of cytochrome P450 2C19 polymorphisms on citalopram/escitalopram exposure: a systematic review and meta-analysis. Clin Pharmacokinet. 2014;53(9):801–11.CrossRefPubMed
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Zurück zum Zitat Goutelle S, Bourguignon L, Bleyzac N, Berry J, Clavel-Grabit F, Tod M. In vivo quantitative prediction of the effect of gene polymorphisms and drug interactions on drug exposure for CYP2C19 substrates. AAPS J. 2013;15(2):415–26.CrossRefPubMedCentralPubMed Goutelle S, Bourguignon L, Bleyzac N, Berry J, Clavel-Grabit F, Tod M. In vivo quantitative prediction of the effect of gene polymorphisms and drug interactions on drug exposure for CYP2C19 substrates. AAPS J. 2013;15(2):415–26.CrossRefPubMedCentralPubMed
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Zurück zum Zitat Tod M, Goutelle S, Gagnieu MC. Genotype-based quantitative prediction of drug exposure for drugs metabolized by CYP2D6. Clin Pharmacol Ther. 2011;90(4):582–7.CrossRefPubMed Tod M, Goutelle S, Gagnieu MC. Genotype-based quantitative prediction of drug exposure for drugs metabolized by CYP2D6. Clin Pharmacol Ther. 2011;90(4):582–7.CrossRefPubMed
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Zurück zum Zitat Castellan AC, Tod M, Gueyffier F, Audars M, Cambriels F, Kassai B, et al. Quantitative prediction of the impact of drug interactions and genetic polymorphisms on cytochrome P450 2C9 substrate exposure. Clin Pharmacokinet. 2013;52(3):199–209.CrossRefPubMed Castellan AC, Tod M, Gueyffier F, Audars M, Cambriels F, Kassai B, et al. Quantitative prediction of the impact of drug interactions and genetic polymorphisms on cytochrome P450 2C9 substrate exposure. Clin Pharmacokinet. 2013;52(3):199–209.CrossRefPubMed
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Zurück zum Zitat Weiss J, Ten Hoevel MM, Burhenne J, Walter-Sack I, Hoffmann MM, Rengelshausen J, et al. CYP2C19 genotype is a major factor contributing to the highly variable pharmacokinetics of voriconazole. J Clin Pharmacol. 2009;49(2):196–204.CrossRefPubMed Weiss J, Ten Hoevel MM, Burhenne J, Walter-Sack I, Hoffmann MM, Rengelshausen J, et al. CYP2C19 genotype is a major factor contributing to the highly variable pharmacokinetics of voriconazole. J Clin Pharmacol. 2009;49(2):196–204.CrossRefPubMed
6.
Zurück zum Zitat Tod M, Nkoud-Mongo C, Gueyffier F. Impact of genetic polymorphism on drug–drug interactions mediated by cytochromes: a general approach. AAPS J. 2013;15(4):1242–52.CrossRefPubMedCentralPubMed Tod M, Nkoud-Mongo C, Gueyffier F. Impact of genetic polymorphism on drug–drug interactions mediated by cytochromes: a general approach. AAPS J. 2013;15(4):1242–52.CrossRefPubMedCentralPubMed
Metadaten
Titel
Quantitative Methods for Prediction of the Effect of Cytochrome P450 Gene Polymorphisms on Substrate Drug Exposure
verfasst von
Sylvain Goutelle
Michel Tod
Publikationsdatum
01.03.2015
Verlag
Springer International Publishing
Erschienen in
Clinical Pharmacokinetics / Ausgabe 3/2015
Print ISSN: 0312-5963
Elektronische ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-014-0217-3

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