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候选基因多态性对注意缺陷多动障碍病程的影响。

Effect of candidate gene polymorphisms on the course of attention deficit hyperactivity disorder.

机构信息

Pediatric Psychopharmacology Department, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Psychiatry Res. 2009 Dec 30;170(2-3):199-203. doi: 10.1016/j.psychres.2008.12.016. Epub 2009 Nov 10.

Abstract

The main aim of this study was to examine the association between attention-deficit hyperactivity disorder (ADHD)-associated genes and the course of ADHD. Subjects were derived from identically designed case-control family studies of boys and girls with ADHD and a genetic linkage study of families with children with ADHD. Caucasian probands and family members with ADHD and with available genetic data were included in this analysis (N=563). The course of ADHD was compared in subjects with and without putative risk alleles (DRD4 7-repeat allele, DAT1 10-repeat allele, and 5HTTLPR long allele). The persistence of ADHD (full or subthreshold diagnosis in the last month) was plotted using Kaplan-Meier survival functions and tested with Cox proportional hazard models. Survival analyses revealed that by 25 years of age 76% of subjects with a DRD4 7-repeat allele were estimated to have significantly more persistent ADHD compared with 66% of subjects without the risk allele. In contrast, there were no significant associations between the course of ADHD and the DAT1 10-repeat allele (P=0.94) and 5HTTLPR long allele. Our findings suggest that the DRD4 7-repeat allele is associated with a more persistent course of ADHD.

摘要

本研究的主要目的是检验注意力缺陷多动障碍(ADHD)相关基因与 ADHD 病程之间的关联。研究对象来源于男孩和女孩 ADHD 的同设计病例对照家族研究,以及 ADHD 患儿家系的遗传连锁研究。本分析纳入了白种先证者及其 ADHD 家族成员,以及具有可用遗传数据的个体(N=563)。比较了具有和不具有假定风险等位基因(DRD4 7 重复等位基因、DAT1 10 重复等位基因和 5HTTLPR 长等位基因)的个体中 ADHD 的病程。使用 Kaplan-Meier 生存函数绘制 ADHD 的持续存在(上个月完全或亚阈值诊断),并使用 Cox 比例风险模型进行检验。生存分析显示,到 25 岁时,76%的 DRD4 7 重复等位基因携带者被估计患有更持续的 ADHD,而无风险等位基因携带者的比例为 66%。相比之下,DAT1 10 重复等位基因(P=0.94)和 5HTTLPR 长等位基因与 ADHD 病程之间无显著关联。我们的研究结果表明,DRD4 7 重复等位基因与 ADHD 病程更持久相关。

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