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association between neuregulin-1 gene variant (rs2439272) and schizophrenia and its negative symptoms in an iranian population
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نویسنده
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yoosefee sadegh ,shahsavand ananloo esmaeil ,joghataei mohammad-taghi ,karimipour morteza ,hadjighassem mahmoudreza ,mohaghghegh hoorie ,tehrani-doost mehdi ,rahimi amir-abbas ,mostafavi abdolmaleky hamid ,hatami maryam
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منبع
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iranian journal of psychiatry - 2016 - دوره : 11 - شماره : 3 - صفحه:147 -153
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چکیده
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objective: although the etiology of schizophrenia is unknown, it has a significant genetic component. a number of studies have indicated that neuregulin-1 (nrg1) gene may play a role in the pathogenesis of schizophrenia. in this study, we examined whether the rs2439272 of nrg1 is associated with schizophrenia and its negative symptoms in an iranian population. method: rs2439272 was genotyped in 469 participants including 276 unrelated patients with schizophrenia and 193 healthy controls. the association of genetic risk with panss, and negative symptoms was examined in the total, male and female samples. cocaphase and clump22 programs were used to compare the allele and genotype frequencies, and general linear regression was used to analyze the quantitative dependent variables by the selected variant. results: in this study, it was revealed that the g allele of rs2439272 might be an allele with the increased risk of developing schizophrenia, especially in the male participants. in addition, significant differences were found between the g allele and gg genotype frequencies and panss, and negative symptoms in the total and male participants. conclusion: our results supported the association between rs2439272 in nrg1 gene and risk of schizophrenia and its negative symptoms in an iranian population.
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کلیدواژه
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negative symptoms ,neuregulin-1 (nrg1) ,positive and negative syndrome scale (panss) ,schizophrenia ,single nucleotide polymorphism (snp)
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آدرس
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neuroscience and neurology research center, qom university of medical sciences, qom, iran. and department of neuroscience, school of advanced technologies in medicine, iran university of medical sciences (iums), tehran, iran. and health and religion research center, qom university of medical sciences, qom, iran., Iran, Islamic Republic of, department of adult psychiatry, roozbeh hospital, school of medicine, tehran university of medical sciences (tums), tehran, iran.and department of genomic psychiatry and behavioral genomics (dgpbg), roozbeh psychiatry hospital, school of medicine, tehran university of medical sciences (tums), tehran, iran., Iran, Islamic Republic of, department of neuroscience, school of advanced technologies in medicine, iran university of medical sciences (iums), tehran, iran., Iran, Islamic Republic of, molecular medicine group, pasteur institute of iran., Iran, Islamic Republic of, department of neuroscience and addiction studies, school of advanced technologies in medicine, tehran university of medical sciences (tums), tehran, iran., Iran, Islamic Republic of, department of neuroscience and addiction studies, school of advanced technologies in medicine, tehran university of medical sciences (tums), tehran, iran., Iran, Islamic Republic of, department of child and adolescent psychiatry, roozbeh hospital, school of medicine, tehran university of medical sciences (tums), tehran, iran., Iran, Islamic Republic of, molecular medicine group, pasteur institute of iran., Iran, Islamic Republic of, department of genetics & genomics, boston university school of medicine, boston, ma, united states., United States, department of adult psychiatry, roozbeh hospital, school of medicine, tehran university of medical sciences (tums), tehran, iran, Iran, Islamic Republic of
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پست الکترونیکی
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esmaeilshahsavand@gmail.com
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Authors
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