Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele

IF 1 4区 生物学 Q4 GENETICS & HEREDITY Annals of Human Genetics Pub Date : 2024-04-16 DOI:10.1111/ahg.12560
Larry Baum, Chi Chiu Lee, Rui Ye, Yuanxin Zhong, Se Fong Hung, Chun Pan Tang, Ting Pong Ho, James M Swanson, Robert K Moyzis, Pak-Chung Sham, Patrick Wing-Leung Leung
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Abstract

To investigate the association of attention-deficit/hyperactivity disorder (ADHD) with the 48-base pair (bp) variable number of tandem repeats (VNTR) in exon 3 of the dopamine receptor D4 (DRD4) gene, we genotyped 240 ADHD patients and their parents from Hong Kong. The 4R allele was most common, followed by 2R. We examined association between the 2R allele (relative to 4R) and ADHD by Transmission Disequilibrium Test (TDT). The odds ratio (OR) (95% confidence interval) was 0.90 (0.64–1.3). The p-value was 0.6. Examining subgroups revealed nominally significant association of 2R with inattentive ADHD: OR = 0.33 (0.12–0.92) and p = 0.03. Because our study used TDT analysis, we meta-analyzed the association of 2R with ADHD in Asians (1329 patient alleles), revealing results similar to ours: OR = 0.97 (0.80–1.2) and p = 0.8. To examine the association of 2R with inattentive ADHD, we meta-analyzed all studies (regardless of analysis type or ethnicity, in order to increase statistical power): 702 patient alleles, 1420 control alleles, OR = 0.81 (0.57–1.1) and p = 0.2. Overall, there is no evidence of association between ADHD and the 2R allele, but the suggestive association with the inattentive type warrants further investigation.

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注意缺陷/多动障碍和多巴胺受体 D4 (DRD4) 第 3 外显子串联重复序列 (VNTR) 2 重复等位基因
为了研究注意力缺陷/多动障碍(ADHD)与多巴胺受体DRD4(Dopamine receptor D4)基因第3外显子中48碱基对(bp)可变串联重复序列(VNTR)的关系,我们对来自香港的240名ADHD患者及其父母进行了基因分型。4R等位基因最常见,其次是2R。我们通过传递不平衡测试(TDT)研究了2R等位基因(相对于4R等位基因)与ADHD之间的关系。几率比(OR)(95% 置信区间)为 0.90(0.64-1.3)。p 值为 0.6。对亚组的研究显示,2R 与注意力不集中型多动症有明显的相关性:OR = 0.33(0.12-0.92),P = 0.03。由于我们的研究使用了TDT分析,因此我们对亚洲人(1329名等位基因患者)2R与多动症的相关性进行了荟萃分析,结果与我们的研究相似:OR = 0.97 (0.80-1.2),P = 0.8。为了研究 2R 与注意力不集中多动症的关系,我们对所有研究进行了荟萃分析(不考虑分析类型或种族,以提高统计能力):702 例患者等位基因,1420 例对照等位基因,OR = 0.81 (0.57-1.1),P = 0.2。总体而言,没有证据表明多动症与 2R 等位基因有关联,但与注意力不集中型之间的提示性关联值得进一步研究。
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来源期刊
Annals of Human Genetics
Annals of Human Genetics 生物-遗传学
CiteScore
4.20
自引率
0.00%
发文量
34
审稿时长
3 months
期刊介绍: Annals of Human Genetics publishes material directly concerned with human genetics or the application of scientific principles and techniques to any aspect of human inheritance. Papers that describe work on other species that may be relevant to human genetics will also be considered. Mathematical models should include examples of application to data where possible. Authors are welcome to submit Supporting Information, such as data sets or additional figures or tables, that will not be published in the print edition of the journal, but which will be viewable via the online edition and stored on the website.
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