Association study of promoter polymorphisms at the dopamine transporter gene in Attention Deficit Hyperactivity Disorder

被引:26
作者
Xu, Xiaohui [1 ]
Mill, Jonathan [1 ]
Sun, Bo [2 ]
Chen, Chih-Ken [3 ]
Huang, Yu-Shu
Wu, Yu-Yu
Asherson, Philip [1 ]
机构
[1] Kings Coll London, Inst Psychiat, MRC Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
[2] Kings Coll London, Sch Med, London WC2R 2LS, England
[3] Chang Gung Mem Hosp, Dept Psychiat, Kaohsiung, Taiwan
基金
英国惠康基金; 英国医学研究理事会;
关键词
DEFICIT/HYPERACTIVITY DISORDER; CANDIDATE GENE; DAT1; REGION; ADHD; DISEQUILIBRIUM; PREVALENCE; HAPLOTYPE; CHILDREN; ALCOHOL;
D O I
10.1186/1471-244X-9-3
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Attention deficit hyperactivity disorder (ADHD) is a complex neurobehavioral disorder. The dopamine transporter gene (DAT1/SLC6A3) has been considered a good candidate for ADHD. Most association studies with ADHD have investigated the 40-base-pair variable number of tandem repeat (VNTR) polymorphism in the 3'-untranslated region of DAT1. Only few studies have reported association between promoter polymorphisms of the gene and ADHD. Methods: To investigate the association between the polymorphisms -67A/T (rs2975226) and -839C/T (rs2652511) in promoter region of DAT1 in ADHD, two samples of ADHD patients from the UK (n = 197) and Taiwan (n = 212) were genotyped, and analysed using within-family transmission disequilibrium test (TDT). Results: A significant association was found between the T allele of promoter polymorphism -67A/T and ADHD in the Taiwanese population (P = 0.001). There was also evidence of preferential transmission of the T allele of -67A/T polymorphism in combined samples from the UK and Taiwan (P = 0.003). No association was detected between the -839C/T polymorphism and ADHD in either of the two populations. Conclusion: The finding suggests that genetic variation in the promoter region of DAT1 may be a risk factor in the development of ADHD.
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页数:5
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