Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: a longitudinal open label trial

Eur J Paediatr Neurol. 2013 Jul;17(4):407-14. doi: 10.1016/j.ejpn.2013.02.002. Epub 2013 Mar 28.

Abstract

The variable number of tandem repeat polymorphism in the 3'-untranslated region of the dopamine transporter gene (DAT) may influence the variability of the therapeutic response to methylphenidate (MPH) in Attention Deficit/Hyperactivity Disorder (ADHD). For this reason we evaluated the neuropsychological functioning after a prolonged period of MPH treatment and after a specific time from MPH suspension. Relationship between DAT VNTR genotypes and neurocognitive response to MPH was analyzed in a sample of 108 drug-naive ADHD patients. The performance of children with ADHD on measures of working memory, inhibition and planning was assessed at 4, 8 and 24 weeks and at 8 weeks after MPH withdrawal. Patients with 9/9 genotype evidenced an improvement in response inhibition and working memory only at 4 weeks of treatment, in planning at 24 weeks of therapy and after 8 weeks of MPH suspension. Patients with 9/10 showed an improvement in response inhibition at 4, 8 and 24 weeks of treatment, in planning at 24 weeks and after 8 weeks of MPH suspension. Patients with 10/10 evidenced an improvement in response inhibition and working memory at 4, 8 and 24 weeks of treatment and in planning at 4, 8 and 24 weeks of treatment and after 8 weeks of suspension. These results indicate that the 9/9 ADHD genotype has a different response at 24 weeks treatment with MPH. 10/10 DAT allele seems to be associated with an increased expression level of the dopamine transporter and seems to mediate the MPH treatment response in ADHD patients.

MeSH terms

  • Adolescent
  • Attention Deficit Disorder with Hyperactivity / complications
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Central Nervous System Stimulants / therapeutic use*
  • Child
  • Cognition Disorders / drug therapy*
  • Cognition Disorders / etiology
  • Cognition Disorders / genetics
  • Dopamine Plasma Membrane Transport Proteins / genetics*
  • Female
  • Genotype
  • Humans
  • Inhibition, Psychological
  • Longitudinal Studies
  • Male
  • Memory, Short-Term / drug effects
  • Methylphenidate / therapeutic use*
  • Minisatellite Repeats / genetics
  • Neuropsychological Tests
  • Pharmacogenetics*
  • Problem Solving / drug effects
  • Psychiatric Status Rating Scales
  • Time Factors

Substances

  • Central Nervous System Stimulants
  • Dopamine Plasma Membrane Transport Proteins
  • Methylphenidate