Skip to main content
Erschienen in: Journal of Neural Transmission 1/2019

18.09.2018 | Translational Neurosciences - Original Article

Genetic validation study of protein tyrosine phosphatase receptor type D (PTPRD) gene variants and risk for antipsychotic-induced weight gain

Erschienen in: Journal of Neural Transmission | Ausgabe 1/2019

Einloggen, um Zugang zu erhalten

Abstract

Schizophrenia is a severe, debilitating disorder with a lifetime prevalence of 1% irrespective of gender or ethnicity and is typically treated with antipsychotic drugs. Antipsychotic-induced weight gain (AIWG) is a leading factor of patient non-compliance and has previously been shown to increase the risk of type 2 diabetes, metabolic syndrome, and cardiovascular events. The current study intends to replicate findings from a recent genome-wide association study in Han-Chinese patients implicating two gene variants (rs10977144 and rs10977154) of the protein tyrosine phosphatase receptor type D (PTPRD) in antipsychotic-induced weight gain (AIWG). We investigated a sample of European and African American ancestry (n = 201) and calculated percentage of weight change using linear regression corrected for type of antipsychotics, duration of treatment and principal components from ancestry checks. As secondary goal, we investigated additional gene variants of PTPRD previously not associated with AIWG. We found no association with rs10977144 and rs10977154. However, we found nominally significant results between PTPRD and AIWG with rs73398242 in Europeans (BETA = − 0.267, p = 0.002) and rs13294608 in African Americans (BETA = 0.423, p = 0.003). According to Haploreg, both SNPs are histone marks for enhancers and promoters across various brain regions including the cingulate gyrus and dorsolateral prefrontal cortex. In summary, our results tentatively suggest that PTPRD might be associated with AIWG although different SNPS might be involved in different ethnic groups.
Literatur
Zurück zum Zitat 1000 Genomes Project Consortium, Abecasis GR, Altshuler D et al (2010) A map of human genome variation from population-scale sequencing. Nature 467:1061–1073CrossRef 1000 Genomes Project Consortium, Abecasis GR, Altshuler D et al (2010) A map of human genome variation from population-scale sequencing. Nature 467:1061–1073CrossRef
Zurück zum Zitat Below JE, Gamazon ER, Morrison JV et al (2011) Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia 54:2047–2055CrossRefPubMedPubMedCentral Below JE, Gamazon ER, Morrison JV et al (2011) Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia 54:2047–2055CrossRefPubMedPubMedCentral
Zurück zum Zitat Chang Y-C, Chiu Y-F, Liu P-H et al (2012) Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort. Clin Endocrinol 76:365–372CrossRef Chang Y-C, Chiu Y-F, Liu P-H et al (2012) Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort. Clin Endocrinol 76:365–372CrossRef
Zurück zum Zitat Cheke LG, Bonnici HM, Clayton NS, Simons JS (2017) Obesity and insulin resistance are associated with reduced activity in core memory regions of the brain. Neuropsychologia 96:137–149CrossRefPubMedPubMedCentral Cheke LG, Bonnici HM, Clayton NS, Simons JS (2017) Obesity and insulin resistance are associated with reduced activity in core memory regions of the brain. Neuropsychologia 96:137–149CrossRefPubMedPubMedCentral
Zurück zum Zitat Czerwensky F, Leucht S, Steimer W (2013) MC4R rs489693: a clinical risk factor for second generation antipsychotic-related weight gain? Int J Neuropsychopharmacol 16:2103–2109CrossRefPubMed Czerwensky F, Leucht S, Steimer W (2013) MC4R rs489693: a clinical risk factor for second generation antipsychotic-related weight gain? Int J Neuropsychopharmacol 16:2103–2109CrossRefPubMed
Zurück zum Zitat Delaneau O, Marchini J, Zagury J-F (2011) A linear complexity phasing method for thousands of genomes. Nat Methods 9:179–181CrossRefPubMed Delaneau O, Marchini J, Zagury J-F (2011) A linear complexity phasing method for thousands of genomes. Nat Methods 9:179–181CrossRefPubMed
Zurück zum Zitat Gonçalves VF, Zai CC, Tiwari AK et al (2014) A hypothesis-driven association study of 28 nuclear-encoded mitochondrial genes with antipsychotic-induced weight gain in schizophrenia. Neuropsychopharmacology 39:1347–1354CrossRefPubMedPubMedCentral Gonçalves VF, Zai CC, Tiwari AK et al (2014) A hypothesis-driven association study of 28 nuclear-encoded mitochondrial genes with antipsychotic-induced weight gain in schizophrenia. Neuropsychopharmacology 39:1347–1354CrossRefPubMedPubMedCentral
Zurück zum Zitat Ikeda M, Tanaka S, Saito T et al (2018) Re-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index. Psychol Med 48:1745–1748CrossRefPubMedPubMedCentral Ikeda M, Tanaka S, Saito T et al (2018) Re-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index. Psychol Med 48:1745–1748CrossRefPubMedPubMedCentral
Zurück zum Zitat Imamura M, Iwata M, Maegawa H et al (2013) Replication study for the association of rs391300 in SRR and rs17584499 in PTPRD with susceptibility to type 2 diabetes in a Japanese population. J Diabetes Investig 4:168–173CrossRefPubMed Imamura M, Iwata M, Maegawa H et al (2013) Replication study for the association of rs391300 in SRR and rs17584499 in PTPRD with susceptibility to type 2 diabetes in a Japanese population. J Diabetes Investig 4:168–173CrossRefPubMed
Zurück zum Zitat Kang SH, Lee J-I, Han HR et al (2014) Polymorphisms of the leptin and HTR2C genes and clozapine-induced weight change and baseline BMI in patients with chronic schizophrenia. Psychiatr Genet 24:249–256CrossRefPubMed Kang SH, Lee J-I, Han HR et al (2014) Polymorphisms of the leptin and HTR2C genes and clozapine-induced weight change and baseline BMI in patients with chronic schizophrenia. Psychiatr Genet 24:249–256CrossRefPubMed
Zurück zum Zitat Kircher M, Witten DM, Jain P et al (2014) A general framework for estimating the relative pathogenicity of human genetic variants. Nat Genet 46:310–315CrossRefPubMedPubMedCentral Kircher M, Witten DM, Jain P et al (2014) A general framework for estimating the relative pathogenicity of human genetic variants. Nat Genet 46:310–315CrossRefPubMedPubMedCentral
Zurück zum Zitat Lett TAP, Wallace TJM, Chowdhury NI et al (2012) Pharmacogenetics of antipsychotic-induced weight gain: review and clinical implications. Mol Psychiatry 17:242–266CrossRefPubMed Lett TAP, Wallace TJM, Chowdhury NI et al (2012) Pharmacogenetics of antipsychotic-induced weight gain: review and clinical implications. Mol Psychiatry 17:242–266CrossRefPubMed
Zurück zum Zitat Lieberman JA, Stroup TS, McEvoy JP et al (2005) Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. N Engl J Med 353:1209–1223CrossRefPubMed Lieberman JA, Stroup TS, McEvoy JP et al (2005) Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. N Engl J Med 353:1209–1223CrossRefPubMed
Zurück zum Zitat Liu L, Chen L, Li Z et al (2014) Association between gene polymorphisms of seven newly identified loci and type 2 diabetes and the correlate quantitative traits in Chinese Dong populations. Iran J Public Health 43:1345–1355PubMedPubMedCentral Liu L, Chen L, Li Z et al (2014) Association between gene polymorphisms of seven newly identified loci and type 2 diabetes and the correlate quantitative traits in Chinese Dong populations. Iran J Public Health 43:1345–1355PubMedPubMedCentral
Zurück zum Zitat Machiela MJ, Chanock SJ (2015) LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants. Bioinformatics 31:3555–3557CrossRefPubMedPubMedCentral Machiela MJ, Chanock SJ (2015) LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants. Bioinformatics 31:3555–3557CrossRefPubMedPubMedCentral
Zurück zum Zitat Malhotra AK, Correll CU, Chowdhury NI et al (2012) Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug—induced weight gain. Arch Gen Psychiatry 69:904–912CrossRefPubMedPubMedCentral Malhotra AK, Correll CU, Chowdhury NI et al (2012) Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug—induced weight gain. Arch Gen Psychiatry 69:904–912CrossRefPubMedPubMedCentral
Zurück zum Zitat Marchini J, Howie B (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499–511CrossRefPubMed Marchini J, Howie B (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499–511CrossRefPubMed
Zurück zum Zitat Nurmi EL, Spilman SL, Whelan F et al (2013) Moderation of antipsychotic-induced weight gain by energy balance gene variants in the RUPP autism network risperidone studies. Transl Psychiatry 3:e274CrossRefPubMedPubMedCentral Nurmi EL, Spilman SL, Whelan F et al (2013) Moderation of antipsychotic-induced weight gain by energy balance gene variants in the RUPP autism network risperidone studies. Transl Psychiatry 3:e274CrossRefPubMedPubMedCentral
Zurück zum Zitat Nyholt DR (2004) A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet 74:765–769CrossRefPubMedPubMedCentral Nyholt DR (2004) A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet 74:765–769CrossRefPubMedPubMedCentral
Zurück zum Zitat Opgen-Rhein C, Brandl EJ, Müller DJ et al (2010) Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample. Pharmacogenomics 11:773–780CrossRefPubMed Opgen-Rhein C, Brandl EJ, Müller DJ et al (2010) Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample. Pharmacogenomics 11:773–780CrossRefPubMed
Zurück zum Zitat Price AL, Patterson NJ, Plenge RM et al (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38:904–909CrossRefPubMed Price AL, Patterson NJ, Plenge RM et al (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38:904–909CrossRefPubMed
Zurück zum Zitat Purcell S, Neale B, Todd-Brown K et al (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81:559–575CrossRefPubMedPubMedCentral Purcell S, Neale B, Todd-Brown K et al (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81:559–575CrossRefPubMedPubMedCentral
Zurück zum Zitat Tiwari AK, Brandl EJ, Weber C et al (2013) Association of a functional polymorphism in neuropeptide Y with antipsychotic-induced weight gain in schizophrenia patients. J Clin Psychopharmacol 33:11–17CrossRefPubMed Tiwari AK, Brandl EJ, Weber C et al (2013) Association of a functional polymorphism in neuropeptide Y with antipsychotic-induced weight gain in schizophrenia patients. J Clin Psychopharmacol 33:11–17CrossRefPubMed
Zurück zum Zitat Tiwari AK, Brandl EJ, Zai CC et al (2016) Association of orexin receptor polymorphisms with antipsychotic-induced weight gain. World J Biol Psychiatry 17:221–229CrossRefPubMed Tiwari AK, Brandl EJ, Zai CC et al (2016) Association of orexin receptor polymorphisms with antipsychotic-induced weight gain. World J Biol Psychiatry 17:221–229CrossRefPubMed
Zurück zum Zitat Tsai F-J, Yang C-F, Chen C-C et al (2010) A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. PLoS Genet 6:e1000847CrossRefPubMedPubMedCentral Tsai F-J, Yang C-F, Chen C-C et al (2010) A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. PLoS Genet 6:e1000847CrossRefPubMedPubMedCentral
Zurück zum Zitat Wallace TJ, Zai CC, Brandl EJ, Müller DJ (2011) Role of 5-HT(2C) receptor gene variants in antipsychotic-induced weight gain. Pharmacogenom Pers Med 4:83–93 Wallace TJ, Zai CC, Brandl EJ, Müller DJ (2011) Role of 5-HT(2C) receptor gene variants in antipsychotic-induced weight gain. Pharmacogenom Pers Med 4:83–93
Zurück zum Zitat Ward LD, Kellis M (2012) HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 40:D930–D934CrossRefPubMed Ward LD, Kellis M (2012) HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 40:D930–D934CrossRefPubMed
Zurück zum Zitat Ward J, Strawbridge RJ, Bailey MES et al (2017) Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia. Transl Psychiatry 7:1264CrossRefPubMedPubMedCentral Ward J, Strawbridge RJ, Bailey MES et al (2017) Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia. Transl Psychiatry 7:1264CrossRefPubMedPubMedCentral
Zurück zum Zitat Winter SR, Yokum S, Stice E et al (2017) Elevated reward response to receipt of palatable food predicts future weight variability in healthy-weight adolescents. Am J Clin Nutr 105:781–789CrossRefPubMedPubMedCentral Winter SR, Yokum S, Stice E et al (2017) Elevated reward response to receipt of palatable food predicts future weight variability in healthy-weight adolescents. Am J Clin Nutr 105:781–789CrossRefPubMedPubMedCentral
Zurück zum Zitat Yu H, Wang L, Lv L et al (2016) Genome-Wide Association Study suggested the PTPRD polymorphisms were associated with weight gain effects of atypical antipsychotic medications. Schizophr Bull 42:814–823CrossRefPubMed Yu H, Wang L, Lv L et al (2016) Genome-Wide Association Study suggested the PTPRD polymorphisms were associated with weight gain effects of atypical antipsychotic medications. Schizophr Bull 42:814–823CrossRefPubMed
Zurück zum Zitat Zhang J-P, Lencz T, Zhang RX et al (2016) Pharmacogenetic associations of antipsychotic drug-related weight gain: a systematic review and meta-analysis. Schizophr Bull 42:1418–1437CrossRefPubMedPubMedCentral Zhang J-P, Lencz T, Zhang RX et al (2016) Pharmacogenetic associations of antipsychotic drug-related weight gain: a systematic review and meta-analysis. Schizophr Bull 42:1418–1437CrossRefPubMedPubMedCentral
Metadaten
Titel
Genetic validation study of protein tyrosine phosphatase receptor type D (PTPRD) gene variants and risk for antipsychotic-induced weight gain
Publikationsdatum
18.09.2018
Erschienen in
Journal of Neural Transmission / Ausgabe 1/2019
Print ISSN: 0300-9564
Elektronische ISSN: 1435-1463
DOI
https://doi.org/10.1007/s00702-018-1921-1

Weitere Artikel der Ausgabe 1/2019

Journal of Neural Transmission 1/2019 Zur Ausgabe

Psychiatry and Preclinical Psychiatric Studies - Review Article

Application of pharmacogenetics in clinical practice: problems and solutions

Psychiatry and Preclinical Psychiatric Studies - Short communication

The role of depression pharmacogenetic decision support tools in shared decision making

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.