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

Xiaohui Xu, Jonathan Mill, Bo Sun, Chih-Ken Chen, Yu-Shu Huang, Yu-Yu Wu, Philip Asherson

Research output: Contribution to journalArticlepeer-review

30 Citations (Scopus)

Abstract

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.
Original languageEnglish
Article number3
Pages (from-to)3
Number of pages1
JournalBMC Psychiatry
Volume9
DOIs
Publication statusPublished - 5 Feb 2009

Fingerprint

Dive into the research topics of 'Association study of promoter polymorphisms at the dopamine transporter gene in Attention Deficit Hyperactivity Disorder'. Together they form a unique fingerprint.

Cite this