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ITIH3基因多态性可能通过改变GLT8D1的表达水平而使人易患精神疾病。

ITIH3 polymorphism may confer susceptibility to psychiatric disorders by altering the expression levels of GLT8D1.

作者信息

Sasayama Daimei, Hori Hiroaki, Yamamoto Noriko, Nakamura Seiji, Teraishi Toshiya, Tatsumi Masahiko, Hattori Kotaro, Ota Miho, Higuchi Teruhiko, Kunugi Hiroshi

机构信息

Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8502, Japan; Department of Psychiatry, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.

Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8502, Japan.

出版信息

J Psychiatr Res. 2014 Mar;50:79-83. doi: 10.1016/j.jpsychires.2013.12.002. Epub 2013 Dec 15.

Abstract

A recent genome-wide analysis indicated that a polymorphism (rs2535629) of ITIH3 showed the strongest association signal with susceptibility to psychiatric disorders in Caucasian populations. The aim of the study was to replicate the association of rs2535629 with schizophrenia and major depressive disorder (MDD) in Japanese subjects. A total of 611 patients with schizophrenia, 868 with MDD, and 1193 healthy controls were successfully genotyped for rs2535629. A significant difference in allele distribution was found between patients with schizophrenia and controls (odds ratio [OR] = 1.21, 95% confidence interval [CI]: 1.05-1.39, P = 0.0077). A similar trend was found for patients with MDD (OR = 1.11, 95% CI: 0.98-1.26, P = 0.092). The allele distribution in the combined patient group (schizophrenia and MDD) was significantly different from that of the control group (OR = 1.15, 95% CI: 1.03-1.28, P = 0.011). Gene expression microarray analysis of whole blood samples in 39 MDD patients and 40 healthy controls showed that rs2535629 has a strong influence on the expression levels of ITIH4 and GLT8D1. The expression levels of GLT8D1 were significantly higher in patients with MDD than in controls (P = 0.021). To our knowledge, the present study showed for the first time the association of rs2535629 with psychiatric disorders in an Asian population. Our findings suggest that rs2535629 influences the susceptibility to psychiatric disorders by affecting the expression level of GLT8D1.

摘要

最近的全基因组分析表明,ITIH3基因的一个多态性位点(rs2535629)在白种人群中与精神疾病易感性显示出最强的关联信号。本研究的目的是在日本受试者中重复验证rs2535629与精神分裂症和重度抑郁症(MDD)的关联。对总共611例精神分裂症患者、868例MDD患者和1193例健康对照成功进行了rs2535629基因分型。在精神分裂症患者与对照之间发现等位基因分布存在显著差异(优势比[OR]=1.21,95%置信区间[CI]:1.05 - 1.39,P = 0.0077)。MDD患者中也发现了类似趋势(OR = 1.11,95% CI:0.98 - 1.26,P = 0.092)。合并患者组(精神分裂症和MDD)的等位基因分布与对照组显著不同(OR = 1.15,95% CI:1.03 - 1.28,P = 0.011)。对39例MDD患者和40例健康对照的全血样本进行基因表达微阵列分析显示,rs2535629对ITIH4和GLT8D1的表达水平有强烈影响。MDD患者中GLT8D1的表达水平显著高于对照组(P = 0.021)。据我们所知,本研究首次在亚洲人群中显示了rs2535629与精神疾病的关联。我们的研究结果表明,rs2535629通过影响GLT8D1的表达水平影响精神疾病易感性。

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