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儿茶酚-O-甲基转移酶在注意缺陷多动障碍中的作用:一项系统的荟萃分析。

Role of COMT in ADHD: a systematic meta-analysis.

作者信息

Sun Hongjuan, Yuan Fangfen, Shen Xuemei, Xiong Guanglian, Wu Jing

机构信息

Key Laboratory of Environment and Health, Ministry of Education & Department of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.

出版信息

Mol Neurobiol. 2014 Feb;49(1):251-61. doi: 10.1007/s12035-013-8516-5. Epub 2013 Aug 2.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a common and highly heritable childhood-onset psychiatric disorder with significant genetic contribution. Considerable evidence has implicated involvement of dopaminergic system and the prefrontal cortex (PFC) in the pathomechanism of ADHD. The catechol-O-methyltransferase (COMT) gene is of particular interest for ADHD as its crucial role in the degradation of dopamine in the PFC. We summarized the reported findings investigating associations between COMT gene and ADHD and performed a meta-analysis of previous studies to assess the overall magnitude and significance of the association.

摘要

注意力缺陷多动障碍(ADHD)是一种常见且具有高度遗传性的儿童期起病的精神障碍,有显著的遗传因素。大量证据表明多巴胺能系统和前额叶皮质(PFC)参与了ADHD的发病机制。儿茶酚-O-甲基转移酶(COMT)基因对ADHD特别重要,因为它在PFC中多巴胺的降解过程中起关键作用。我们总结了已报道的关于COMT基因与ADHD关联的研究结果,并对先前的研究进行了荟萃分析,以评估该关联的总体强度和显著性。

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