Sleep and COMT polymorphism in ADHD children: preliminary actigraphic data

J Am Acad Child Adolesc Psychiatry. 2006 Aug;45(8):982-989. doi: 10.1097/01.chi.0000220848.48650.10.

Abstract

Objective: To examine whether COMT (catechol-O-methyltransferase) polymorphism modulates aspects of sleep in children diagnosed with attention-deficit/hyperactivity disorder (ADHD).

Method: Nightly sleep actigraphic recordings during a double-blind, placebo-controlled, crossover clinical study (1 week of 0.5 mg/kg MPH; 1 week of placebo) were obtained for 34 children, 7.4 to 12 years old, diagnosed with ADHD (DSM-IV). Diagnosis was generated by the Diagnostic Interview Schedule for Children and was confirmed by multidisciplinary consensus.

Results: Children who were Val allele carriers had poorer sleep continuity compared with children with the Met-Met genotype while receiving a placebo and while receiving methylphenidate.

Conclusions: The findings of the present study support the hypothesis that sleep disturbances in children with ADHD are related to the underlying pathophysiology of the disorder.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Attention Deficit Disorder with Hyperactivity / diagnosis
  • Attention Deficit Disorder with Hyperactivity / drug therapy
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Catechol O-Methyltransferase / genetics*
  • Central Nervous System Stimulants / therapeutic use
  • Child
  • Cross-Over Studies
  • Diagnostic and Statistical Manual of Mental Disorders
  • Double-Blind Method
  • Female
  • Genotype
  • Humans
  • Male
  • Methylphenidate / therapeutic use
  • Polymorphism, Genetic / genetics*
  • Polysomnography
  • Sleep / physiology*

Substances

  • Central Nervous System Stimulants
  • Methylphenidate
  • Catechol O-Methyltransferase