کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4185872 1608131 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Polymorphisms in NRGN are associated with schizophrenia, major depressive disorder and bipolar disorder in the Han Chinese population
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی روانپزشکی و بهداشت روانی
پیش نمایش صفحه اول مقاله
Polymorphisms in NRGN are associated with schizophrenia, major depressive disorder and bipolar disorder in the Han Chinese population
چکیده انگلیسی


• Two SNPs of NRGN were associated with major depression and bipolar disorder.
• A risk haplotype was shared by schizophrenia, major depression, bipolar disorder.
• Rs12807809 was not a risk locus in Han Chinese population.
• NRGN was a common susceptibility gene for major psychiatric disorders.

BackgroundThe NRGN gene locates on 11q24 and encodes a postsynaptic protein kinase substrate that binds calmodulin in the absence of calcium. In a previous genome-wide association study of schizophrenia in the Caucasian population, rs12807809 of NRGN was found to be significantly associated with schizophrenia, moreover, it was further found to be associated with bipolar disorder.MethodsWe recruited 1248 schizophrenia cases, 1344 bipolar disorder cases, 1056 major depressive disorder cases, and 1248 healthy controls from Han Chinese population. Rs12807809 and another two tag SNPs of NRGN were genotyped and analyzed in three diseases respectively. A meta-analysis of rs12807809 was also conducted to verify its association with schizophrenia in Han Chinese population.ResultsRs7113041 was associated with bipolar disorder (odds ratio, 95% confidence interval (OR, 95% CI)=1.194, 1.032–1.383; Pgenotype=0.0126), and rs12278912 was associated with major depressive disorder (OR, 95% CI=0.789, 0.673–0.924; Pallele=0.0102, Pgenotype=0.0399) after Bonferroni correction. The “GA” haplotype of rs7113041–rs12278912 was significantly associated with schizophrenia, major depressive disorder and bipolar disorder (corresponding P values were 2.85E−04, 3.00E−03, and 5.40E−04 after Bonferroni correction).LimitationsDespite the association between NRGN and psychoses we have found, we failed to validate the positive variant rs12807809, which was reported in the Caucasian genome-wide association study both in our single site association test and the meta-analysis. Functional studies are needed to illuminate the role of NRGN in the pathogenesis of these mental disorders.ConclusionsOur findings prove that NRGN is a shared susceptibility gene of schizophrenia, major depression and bipolar disorder in Han Chinese, and this might provide a new target for the diagnosis and treatment of these mental disorders.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Affective Disorders - Volume 194, April 2016, Pages 180–187
نویسندگان
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