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Genetic validation study of protein tyrosine phosphatase receptor type D (PTPRD) gene variants and risk for antipsychotic-induced weight gain.
Maciukiewicz, Malgorzata; Gorbovskaya, Ilona; Tiwari, Arun K; Zai, Clement C; Freeman, Natalie; Meltzer, Herbert Y; Kennedy, James L; Müller, Daniel J.
Afiliação
  • Maciukiewicz M; Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, 250 College Street, R-132, Toronto, ON, M5T1R8, Canada.
  • Gorbovskaya I; Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, 250 College Street, R-132, Toronto, ON, M5T1R8, Canada.
  • Tiwari AK; Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, 250 College Street, R-132, Toronto, ON, M5T1R8, Canada.
  • Zai CC; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
  • Freeman N; Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, 250 College Street, R-132, Toronto, ON, M5T1R8, Canada.
  • Meltzer HY; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
  • Kennedy JL; Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, 250 College Street, R-132, Toronto, ON, M5T1R8, Canada.
  • Müller DJ; Department of Psychiatry and Behavioral Sciences, Northwestern University, Chicago, IL, USA.
J Neural Transm (Vienna) ; 126(1): 27-33, 2019 01.
Article em En | MEDLINE | ID: mdl-30229349
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Antipsicóticos / Negro ou Afro-Americano / Aumento de Peso / População Branca / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Proteínas Tirosina Fosfatases Classe 2 Semelhantes a Receptores / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Antipsicóticos / Negro ou Afro-Americano / Aumento de Peso / População Branca / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Proteínas Tirosina Fosfatases Classe 2 Semelhantes a Receptores / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article