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哌甲酯反应型注意力缺陷/多动障碍中DRD4基因的家系关联研究。

Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder.

作者信息

Leung Patrick Wing-Leung, Chan Janice Ka Yan, Chen Lu Hua, Lee Chi Chiu, Hung Se Fong, Ho Ting Pong, Tang Chun Pan, Moyzis Robert K, Swanson James M

机构信息

Department of Psychology, The Chinese University of Hong Kong, Hong Kong, PRC.

The Duchess of Kent Children's Hospital at Sandy Bay, Hospital Authority, Hong Kong, PRC.

出版信息

PLoS One. 2017 Mar 10;12(3):e0173748. doi: 10.1371/journal.pone.0173748. eCollection 2017.

Abstract

The 48-basepair (48-bp) variable number tandem repeat (VNTR) polymorphism in exon 3 of the dopamine receptor D4 gene (DRD4) is implicated in the etiology of attention-deficit/ hyperactivity disorder (ADHD). In particular, ADHD in European-ancestry population is associated with an increased prevalence of the 7-repeat (7R) allele of the exon 3 VNTR. However, it is intriguing to note that the 7R allele has been found to be of very low prevalence in the Chinese general population. In a previous case-control study, our research team had found that the 7R allele was similarly absent in Chinese ADHD children in Hong Kong. Instead, there was an increased prevalence of the 2R allele in Chinese ADHD children. Interestingly, in Asian samples, the 2R allele had been found to be an evolutionary derivative of the 7R allele with equivalent biochemical functionality. So, the finding of an association between ADHD and 2R allele in Chinese population does not exactly contradict the original 7R allele finding in European-ancestry population. However, given the potential pitfall of population stratification in the previous case-control design, this current study tested the 2R allele and ADHD association using a methodologically more rigorous family-based approach on 33 Chinese ADHD probands who had favorable clinical responses to stimulant medication (methylphenidate). Haplotype Relative Risk (HRR) analysis and Transmission Disequilibrium Test (TDT) both showed a significant preferential transmission of the 2R allele from the biological parents to ADHD probands (pone-tailed = 0.038, OR = 2.04; pone-tailed = 0.048, OR = 2.29, respectively). A second hypothesis speculates that it is the deviation, including 7R and 2R alleles, from the conserved ancestral 4R allele which confers risk to ADHD. Thus, a preferential transmission of non-4R alleles, against the 4R allele, from biological parents to their ADHD probands is predicted. Both HRR analysis and TDT confirmed such prediction (pone-tailed = 0.029, OR = 2.07; pone-tailed = 0.032, OR = 2.43, respectively). This study re-confirmed the original finding of a previous study that in Chinese population, the 2R allele of the DRD4 exon 3 VNTR was related to ADHD. This endorses the general thesis that DRD4 exon 3 VNTR polymorphism is related to ADHD, despite that the exact length or number of repeats of the associated alleles varies across ethnicity. This in turn supports the dopamine dysregulation theory of ADHD.

摘要

多巴胺受体D4基因(DRD4)外显子3中的48个碱基对(48-bp)可变数目串联重复序列(VNTR)多态性与注意力缺陷多动障碍(ADHD)的病因有关。特别是,欧洲裔人群中的ADHD与外显子3 VNTR的7重复(7R)等位基因的患病率增加有关。然而,有趣的是,在中国普通人群中发现7R等位基因的患病率非常低。在之前的一项病例对照研究中,我们的研究团队发现,香港的中国ADHD儿童中同样不存在7R等位基因。相反,中国ADHD儿童中2R等位基因的患病率有所增加。有趣的是,在亚洲样本中,2R等位基因被发现是7R等位基因的进化衍生物,具有同等的生化功能。因此,在中国人群中发现ADHD与2R等位基因之间的关联并不完全与在欧洲裔人群中最初发现的7R等位基因相矛盾。然而,鉴于之前病例对照设计中存在人群分层的潜在陷阱,本研究采用了一种方法上更严谨的基于家系的方法,对33名对兴奋剂药物(哌甲酯)有良好临床反应的中国ADHD先证者进行了2R等位基因与ADHD关联的测试。单倍型相对风险(HRR)分析和传递不平衡检验(TDT)均显示2R等位基因从生物学父母向ADHD先证者有显著的优先传递(单尾检验P值分别为=0.038,OR=2.04;单尾检验P值=0.048,OR=2.29)。第二个假设推测,是包括7R和2R等位基因在内的与保守的祖先4R等位基因的偏差赋予了ADHD风险。因此,预计非4R等位基因相对于4R等位基因会从生物学父母向其ADHD先证者有优先传递。HRR分析和TDT均证实了这一预测(单尾检验P值分别为=0.029,OR=2.07;单尾检验P值=0.032,OR=2.43)。本研究再次证实了之前一项研究的最初发现,即在中国人中,DRD4外显子3 VNTR的2R等位基因与ADHD有关。这支持了一个普遍的观点,即DRD4外显子3 VNTR多态性与ADHD有关,尽管相关等位基因的确切长度或重复次数因种族而异。这反过来支持了ADHD的多巴胺调节异常理论。

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