中国人注意缺陷多动障碍与儿茶酚- o -甲基转移酶基因无相关性。

San-Duo Jiang, Xiao-Dong Wu, Ye Zhang, Guo-Mei Tang, Yi-Ping Qian, Dong-Xiang Wang
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引用次数: 0

摘要

以往的研究表明,儿茶酚胺能系统可能参与了注意力缺陷多动障碍(ADHD)的发病机制。由于catecheler - o -methyltransferase (COMT)是一种参与多巴胺能和去甲肾上腺素能系统中儿茶酚胺能神经递质的降解的酶,因此COMT可能在ADHD中发挥作用。为了验证这一假设,我们使用了两种基于家庭的分析,即传播不平衡检验(TDT)和基于单倍型的单倍型相对风险(HHRR),以检验由79名ADHD先证者及其父母组成的中国样本中COMT基因与dsm - iv诊断的ADHD之间可能的关联。TDT (chi2 = 1.03, df=1, P > 0.05)和HHRR (chi2 = 1.08, df=1, P > 0.05)分析均未发现COMT等位基因优先传播给ADHD儿童。我们的数据表明,在中国人群中,ADHD和COMT基因之间没有关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.

Previous studies suggested that the catecholaminergic systems may be involved in the pathogenesis of attention-deficit hyperactivity disorder(ADHD). Since catechel-O-methyltransferase (COMT) is an enzyme involved in the degradation of catecholaminergic neurotransmitters of the dopaminergic and noradrenergic systems,it is possible that COMT may play a role in ADHD. To test this hypothesis, we used two family-based analyses,the transmission disequilibrium test (TDT) and the haplotype-based haplotype relative risk (HHRR), to examine the possible association between COMT gene and DSM-IV-diagnosed ADHD in a Chinese sample consisting of 79 ADHD probands and their parents. Both TDT (chi2 = 1.03, df=1, P > 0.05) and HHRR (chi2 = 1.08, df = 1, P > 0.05) analyses failed to detect preferential transmission of a COMT allele to the ADHD children. Our data suggested that there was no association between ADHD and the COMT gene in the Chinese population.

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