Lack of association of the dopamine transporter gene in a French ADHD sample

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1509-10. doi: 10.1002/ajmg.b.30695.

Abstract

Discrepancies in the role of the 40 bp VNTR polymorphism of the dopamine transporter gene (DAT1) in attention-deficit hyperactivity disorder (ADHD) could be due to various sources of genetic or phenotypical heterogeneity. We therefore analyzed a sample of 146 ADHD children and their parents, with a transmission disequilibrium test (TDT) design, assessing age, inattention, and hyperactivity dimensions and total score of the ADHD Rating Scale, the number of errors and the total score at Stroop Color-Word test, and the total score at the Trail Making Test. The TDT for 10-repeat (10-R) allele shows a perfect lack of transmission bias (Mc Nemar chi(2) = 0) and PBAT analyses showed no role of this polymorphism for any of the studied endophenotypes. Lack of statistical power is always a possibility, but with a sample size above the average of the majority of previous studies, and an odds ratio (number of transmitted versus untransmitted 10-R allele) of 1.00 exactly, this possibility may be considered as not very likely.

MeSH terms

  • Adolescent
  • Alleles
  • Attention Deficit Disorder with Hyperactivity / diagnosis
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Chi-Square Distribution
  • Child
  • Confidence Intervals
  • Dopamine Plasma Membrane Transport Proteins / genetics*
  • Female
  • France
  • Genetic Predisposition to Disease*
  • Humans
  • Linkage Disequilibrium
  • Male
  • Microsatellite Repeats
  • Mothers / statistics & numerical data
  • Odds Ratio
  • Polymorphism, Genetic
  • Severity of Illness Index

Substances

  • Dopamine Plasma Membrane Transport Proteins
  • SLC6A3 protein, human