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儿茶酚-O-甲基转移酶(COMT)基因Val158Met与精神疾病的关联:一项综合荟萃分析。

Association between COMT Val158Met and psychiatric disorders: A comprehensive meta-analysis.

作者信息

Taylor Steven

机构信息

University of British Columbia, British Columbia, Canada.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2018 Mar;177(2):199-210. doi: 10.1002/ajmg.b.32556. Epub 2017 Jun 13.

Abstract

Catechol-O-methyltransferase (COMT) Val158Met is widely regarded as potentially important for understanding the genetic etiology of many different psychiatric disorders. The present study appears to be the first comprehensive meta-analysis of COMT genetic association studies to cover all psychiatric disorders for which there were available data, published in any language, and with an emphasis on investigating disorder subtypes (defined clinically or by demographic or other variables). Studies were included if they reported one or more datasets (i.e., some studies examined more than one clinical group) in which there were sufficient information to compute effect sizes. A total of 363 datasets were included, consisting of 56,998 cases and 74,668 healthy controls from case control studies, and 2,547 trios from family based studies. Fifteen disorders were included. Attention-deficit hyperactivity disorder and panic disorder were associated with the Val allele for Caucasian samples. Substance-use disorder, defined by DSM-IV criteria, was associated with the Val allele for Asian samples. Bipolar disorder was associated with the Met allele in Asian samples. Obsessive-compulsive disorder tended to be associated with the Met allele only for males. There was suggestive evidence that the Met allele is associated with an earlier age of onset of schizophrenia. Results suggest pleiotropy and underscore the importance of examining subgroups-defined by variables such as age of onset, sex, ethnicity, and diagnostic system-rather than examining disorders as monolithic constructs.

摘要

儿茶酚-O-甲基转移酶(COMT)基因Val158Met多态性被广泛认为对于理解多种不同精神疾病的遗传病因具有潜在重要性。本研究似乎是对COMT基因关联研究的首次全面荟萃分析,涵盖了所有有可用数据的精神疾病,无论数据以何种语言发表,并着重于研究疾病亚型(根据临床定义或人口统计学或其他变量定义)。如果研究报告了一个或多个数据集(即一些研究检查了不止一个临床组),且其中有足够信息来计算效应量,则纳入该研究。总共纳入了363个数据集,包括来自病例对照研究的56,998例病例和74,668例健康对照,以及来自家系研究的2,547个三联体。纳入了15种疾病。注意力缺陷多动障碍和惊恐障碍在白种人样本中与Val等位基因相关。根据《精神疾病诊断与统计手册》第四版(DSM-IV)标准定义的物质使用障碍在亚洲样本中与Val等位基因相关。双相情感障碍在亚洲样本中与Met等位基因相关。强迫症仅在男性中倾向于与Met等位基因相关。有提示性证据表明Met等位基因与精神分裂症的发病年龄较早有关。结果表明存在基因多效性,并强调了检查由发病年龄、性别、种族和诊断系统等变量定义的亚组的重要性,而不是将疾病作为单一整体结构来研究。

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