Functional effects of the DAT1 polymorphism on EEG measures in ADHD

J Am Acad Child Adolesc Psychiatry. 2003 Aug;42(8):986-93. doi: 10.1097/01.CHI.0000046890.27264.88.

Abstract

Objective: This paper examines whether dopamine transporter gene (DAT1) allele status mediates medication-related change in cognitive and neurophysiological measures among children with attention-deficiency/hyperactivity disorder (ADHD).

Method: A single 10-mg dose of methylphenidate was given in a double-blind, placebo-controlled fashion to children with ADHD who were seen for cognitive testing and EEG recording. Buccal samples were obtained and genotyped for the DAT1 polymorphism.

Results: DAT1 allele status was associated with performance on a sustained attention task and medication-related EEG changes. Compared with those with one or more copies of the DAT1 9-repeat allele (9R), children with two copies of the 10-repeat allele (10R) exhibited poorer performance on the vigilance task. In addition, children with 10R exhibited medication-related EEG changes of increased central and parietal beta power, decreased right frontal theta power, and lower theta/beta ratios; 9R carriers showed the opposite pattern.

Conclusions: The data suggest that the DAT1 polymorphism mediates medication-related changes in cortical activity among children with ADHD.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Attention Deficit Disorder with Hyperactivity / drug therapy
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Central Nervous System Stimulants / therapeutic use
  • Child
  • Cognition Disorders / diagnosis
  • Dopamine Plasma Membrane Transport Proteins
  • Double-Blind Method
  • Electroencephalography*
  • Female
  • Humans
  • Male
  • Membrane Glycoproteins*
  • Membrane Transport Proteins / genetics*
  • Methylphenidate / therapeutic use
  • Nerve Tissue Proteins*
  • Neuropsychological Tests
  • Polymorphism, Genetic / genetics*

Substances

  • Central Nervous System Stimulants
  • Dopamine Plasma Membrane Transport Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • SLC6A3 protein, human
  • Methylphenidate