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多巴胺转运体基因启动子多态性与注意力缺陷多动障碍关联的重复验证。

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

作者信息

Doyle Christopher, Brookes Keeley, Simpson Jennifer, Park Joanne, Scott Sarah, Coghill David R, Hawi Ziarah, Kirley Aiveen, Gill Michael, Kent Lindsey

机构信息

Bute Medical School, University of St Andrews, Westburn Lane, St Andrews, Scotland KY16 9TS, United Kingdom.

出版信息

Neurosci Lett. 2009 Sep 22;462(2):179-81. doi: 10.1016/j.neulet.2009.06.084. Epub 2009 Jul 2.

Abstract

Genetic associations for Attention Deficit Hyperactivity Disorder (ADHD), a common highly heritable childhood behavioural disorder, require replication in order to establish whether they are true positive findings. The current study aims to replicate recent association findings from the International Multi-centre ADHD Genetics (IMAGE) project in one of the most studied genes related to ADHD, the dopamine transporter (DAT1) gene. In a family-based sample of 450 ADHD probands, three Single Nucleotide Polymorphism (SNP) markers have been genotyped using TaqMan assays. Transmission Disequilibrium Test analysis demonstrates that one of three SNP markers (rs11564750) in the 5' promoter region of the gene is significantly associated with ADHD (P=0.02). This provides further evidence that in addition to the well-known and investigated 3'UTR polymorphism associated with ADHD, there is potentially a further association signal emanating from the 5' promoter region of the gene. Further replication and functional studies are now required to fully understand the consequence of polymorphisms present at both the 5' and 3' ends of the DAT1 gene and their role in ADHD pathophysiology.

摘要

注意缺陷多动障碍(ADHD)是一种常见的、具有高度遗传性的儿童行为障碍,其基因关联需要进行重复验证,以确定它们是否为真正的阳性发现。当前研究旨在对国际多中心ADHD遗传学(IMAGE)项目最近的关联研究结果进行重复验证,该研究涉及与ADHD相关的研究最多的基因之一——多巴胺转运体(DAT1)基因。在一个包含450名ADHD先证者的家系样本中,使用TaqMan分析对三个单核苷酸多态性(SNP)标记进行了基因分型。传递不平衡检验分析表明,该基因5'启动子区域的三个SNP标记之一(rs11564750)与ADHD显著相关(P = 0.02)。这进一步证明,除了与ADHD相关的、已广为人知且经过研究的3'非翻译区多态性外,该基因的5'启动子区域可能还存在另一个关联信号。现在需要进一步的重复验证和功能研究,以全面了解DAT1基因5'和3'末端存在的多态性的后果及其在ADHD病理生理学中的作用。

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