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PMID: 15305167 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes.

Bilder RM, Volavka J, Lachman HM, Grace AA

Abstract

Diverse phenotypic associations with the catechol-O-methyltransferase (COMT) Val158Met polymorphism have been reported. We suggest that some of the complex effects of this polymorphism be understood from the perspective of the tonic-phasic dopamine (DA) hypothesis. We hypothesize that the COMT Met allele (associated with low enzyme activity) results in increased levels of tonic DA and reciprocal reductions in phasic DA in subcortical regions and increased D1 transmission cortically. This pattern of effects is hypothesized to yield increased stability but decreased flexibility of neural network activation states that underlie important aspects of working memory and executive functions; these effects may be beneficial or detrimental depending on the phenotype, a range of endogenous factors, and environmental exigencies. The literature on phenotypic associations of the COMT Val158Met polymorphism is reviewed, highlighting areas where this hypothesis may have explanatory value, and pointing to possible directions for refinement of relevant phenotypes and experimental evaluation of this hypothesis.

MeSH Terms
Animals Catechol O-Methyltransferase/genetics,metabolism Dopamine/genetics,metabolism Humans Mental Disorders/enzymology,genetics Phenotype Polymorphism, Genetic/physiology
Chemicals
Catechol O-Methyltransferase Dopamine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bilder Robert M
Department of Psychiatry, David Geffen School of Medicine and Psychology, UCLA Neuropsychiatric Institute, University of California at Los Angeles, Los Angeles, CA, USA. [email protected]
Volavka Jan
Lachman Herbert M
Grace Anthony A
Article Info
Journal
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Abbr.
Neuropsychopharmacology
ISSN
0893-133X
Published
2004-11-00
Pages
1943-61
Language
English
Region
England
NLM ID
8904907
Subset
IM
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