Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

Mol Psychiatry. 2005 Jun;10(6):598-605. doi: 10.1038/sj.mp.4001615.

Abstract

The available data from preclinical and pharmacological studies on the role of the C-O-methyl transferase (COMT) support the hypothesis that abnormal catecholamine transmission has been implicated in the pathogenesis of mood disorders (MD). We examined the relationship of a common functional polymorphism (Val108/158Met) in the COMT gene, which accounts for four-fold variation in enzyme activity, with 'early-onset' (EO) forms (less than or equal to 25 years) of MD, including patients with major depressive disorder (EO-MDD) and bipolar patients (EO-BPD), in a European multicenter case-control sample. Our sample includes 378 MDD (120 EO-MDD), 506 BPD (222 EO-BPD) and 628 controls. An association was found between the high-activity COMT Val allele, particularly the COMT Val/Val genotype and EO-MDD. These findings suggest that the COMT Val/Val genotype may be involved in EO-MDD or may be in linkage disequilibrium with a different causative polymorphism in the vicinity. The COMT gene may have complex and pleiotropic effects on susceptibility and symptomatology of neuropsychiatric disorders.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Amino Acid Substitution / genetics
  • Bipolar Disorder / enzymology
  • Bipolar Disorder / genetics*
  • Case-Control Studies
  • Catechol O-Methyltransferase / genetics*
  • Depressive Disorder, Major / enzymology
  • Depressive Disorder, Major / genetics*
  • Europe
  • Female
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Linkage Disequilibrium / genetics*
  • Male
  • Polymorphism, Single Nucleotide / genetics*
  • Reference Values
  • Risk Factors

Substances

  • Catechol O-Methyltransferase