Catechol-O-methyl transferase and schizophrenia

Psychiatr Danub. 2010 Jun;22(2):270-4.

Abstract

Catechol-O-methyl transferase (COMT) is an enzyme involved in the degradation of dopamine. The most commonly examined polymorphism within the COMT gene is Val108/158Met polymorphism, which results in three to fourfold difference in COMT enzyme activity. It is particularely important in prefrontal cortex, since COMT activity is the most important regulator of the prefrontal dopamine function. Given the association between schizophrenia and decreased dopamine activity in the prefrontal cortex, it is not surprising that Val108/158Met polymorphism is among the most extensively investigated polymorphisms in schizophrenia. According to different studies, Val allele may be a small risk factor for schizophrenia. There is also some evidence that Val108/158Met polymorphism influences the age of onset of schizophrenia, cognitive function, severity of psychotic symptoms, as well as efficacy and adverse events of antipsychotics. Heterogenity of patient population has undoubtedly influenced the results of these studies. Interaction of Val108/158Met polymorphism with other genes and environmental factors is an important avenue for future research.

Publication types

  • Review

MeSH terms

  • Age of Onset
  • Alleles*
  • Antipsychotic Agents / adverse effects
  • Antipsychotic Agents / therapeutic use
  • Catechol O-Methyltransferase / genetics*
  • Chromosomes, Human, Pair 22 / genetics
  • Cognition Disorders / drug therapy
  • Cognition Disorders / genetics
  • Cognition Disorders / physiopathology
  • Dopamine / metabolism
  • Humans
  • Pharmacogenetics
  • Polymorphism, Genetic / genetics*
  • Prefrontal Cortex / physiopathology
  • Prognosis
  • Schizophrenia / drug therapy
  • Schizophrenia / genetics*
  • Schizophrenia / physiopathology
  • Treatment Outcome

Substances

  • Antipsychotic Agents
  • Catechol O-Methyltransferase
  • Dopamine