No association between the DAT1 10-repeat allele and ADHD in the Iranian population

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):110-1. doi: 10.1002/ajmg.b.30578.

Abstract

Association studies between attention-deficit hyperactivity disorder (ADHD) and the 10-repeat allele of a polymorphism (a 40 bp variable number of tandem repeats) in the dopamine transporter gene (DAT1) have resulted in mixed findings in different populations. We performed a case/control study to clarify the contribution of this allele with ADHD in the Iranian population. No association was observed between the 10-allele and disease (chi(2) = 0.081, P < 0.9). Furthermore, no significant difference was observed in the homozygosity of this allele between the case and control groups (chi(2) = 0.022, P < 0.9). Implication of the dopamine transporter gene in the pathophysiology of ADHD warrants investigation of other functional polymorphisms within this gene in the Iranian ADHD patients.

MeSH terms

  • Adolescent
  • Alleles*
  • Attention Deficit Disorder with Hyperactivity / ethnology
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Case-Control Studies
  • Child
  • Dopamine Plasma Membrane Transport Proteins / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Iran
  • Male
  • Polymorphism, Genetic
  • Population Groups / genetics

Substances

  • Dopamine Plasma Membrane Transport Proteins
  • SLC6A3 protein, human