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Specific and common genes implicated across major mental disorders: A review of meta-analysis studies

机译:涉及主要精神障碍的具体和常见基因:荟萃分析研究综述

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Major efforts have been directed at family-based association and case control studies to identify the involvement of candidate genes in the major disorders of mental health. What remains unknown is whether candidate genes are associated with multiple disorders via pleiotropic mechanisms, and/or if other genes are specific to susceptibility for individual disorders. Here we undertook a review of genes that have been identified in prior meta-analyses examining specific genes and specific mental disorders that have core disruptions to emotional and cognitive function and contribute most to burden of illness major depressive disorder (MDD), anxiety disorders (AD, including panic disorder and obsessive compulsive disorder), schizophrenia (SZ) and bipolar disorder (BD) and attention deficit hyperactivity disorder (ADHD). A literature review was conducted up to end-March 2013 which included a total of 1519 meta-analyses across 157 studies reporting multiple genes implicated in one or more of the five disorders studied. A total of 134 genes (206 variants) were identified as significantly associated risk variants for MDD, AD, ADHD, SZ or BD. Null genetic effects were also reported for 195 genes (426 variants). 13 genetic variants were shared in common between two or more disorders (APOE e4, ACE Ins/Del, BDNF Val66Met, COMT Val158Mer, DAOA G72/G30 rs3918342, DAT1 40-bp, DRD4 48-bp, SLC6A4 5-HTTLPR, HTR1A C1019G, MTHR C677T, MTHR A1298C, SLC6A4 VNTR and TPH1 218A/C) demonstrating evidence for pleiotrophy. Another 12 meta-analyses of GWAS studies of the same disorders were identified, with no overlap in genetic variants reported. This review highlights the progress that is being made in identifying shared and unique genetic mechanisms that contribute to the risk of developing several major psychiatric disorders, and identifies further steps for progress. (C) 2014 Elsevier Ltd. All rights reserved.
机译:主要的努力是针对基于家庭的协会和案例控制研究,以确定候选基因参与心理健康的主要障碍。仍然未知的是候选基因是否通过磷酸化机制与多种疾病相关,和/或其他基因对个体疾病的易感性特异。在这里,我们对先前的Meta分析中鉴定的基因进行了审查,检查了对情绪和认知功能的核心中断的特定基因和特异性精神障碍,并为疾病重症抑郁症(MDD),焦虑症(广告)有助于最多,包括恐慌障碍和强迫症),精神分裂症(SZ)和双相障碍(BD)和注意力缺陷多动障碍(ADHD)。文献综述是在2013年底末期进行的,其中包括跨157项研究总共1519分析,报告了在研究中的五种疾病中的一种或多种中涉及的多种基因。共有134个基因(206个变体)被鉴定为MDD,AD,ADHD,SZ或BD的显着相关的风险变量。还报告了NULL遗传效应195个基因(426个变体)。 13种遗传变异在两种或更多次疾病之间共用(Apoe E4,Ace Ins / Del,BDNF Val66met,Comt Val158mer,Daoa G72 / G30 RS3918342,DAT1 40-BP,DRD4 48-BP,SLC6A4 5-HTTLPR,HTR1A C1019G ,MTHR C677T,MTHR A1298C,SLC6A4 VNTR和TPH1 218A / c)展示了肺炎的证据。鉴定了另外12个荟萃分析的GWAS研究,同一疾病的研究,报告的遗传变异中没有重叠。本综述强调了识别共享和独特遗传机制的进展,这有助于开发几个主要精神疾病的风险,并确定进展的进一步措施。 (c)2014年elestvier有限公司保留所有权利。

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