No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.

San-Duo Jiang, Xiao-Dong Wu, Ye Zhang, Guo-Mei Tang, Yi-Ping Qian, Dong-Xiang Wang
{"title":"No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.","authors":"San-Duo Jiang,&nbsp;Xiao-Dong Wu,&nbsp;Ye Zhang,&nbsp;Guo-Mei Tang,&nbsp;Yi-Ping Qian,&nbsp;Dong-Xiang Wang","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":23770,"journal":{"name":"Yi chuan xue bao = Acta genetica Sinica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2005-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Yi chuan xue bao = Acta genetica Sinica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Influence of B mating-type factor on recovery of nuclear types from dikaryons in Lentinula edodes]. [Expression and immunization testing of fusion protein of Newcastle disease virus in leaf tissue of transgenic rice]. Nuclear matrices and matrix attachment regions from Green alga: Dunaliella salina. [Molecular basic of interaction between disease resistance gene and avirulence gene]. [Progress in the study on diacylgycerol acyltransferase (DGAT)-related genes].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1