Literature DB >> 21769726

Importance of the COMT gene for sex differences in brain function and predisposition to psychiatric disorders.

Elizabeth M Tunbridge1, Paul J Harrison.   

Abstract

As outlined elsewhere in this volume, sex differences can affect brain function and its dysfunction in psychiatric disorders. It is known that genetic factors contribute to these sex dimorphisms, but the individual genes have rarely been identified. The catechol-O-methyltransferase (COMT) gene, which encodes an enzyme that metabolises catechol compounds, including dopamine, is a leading candidate in this regard. COMT's enzyme activity, and the neurochemistry and behaviour of COMT knockout mice are both markedly sexually dimorphic. Furthermore, genetic associations between COMT and psychiatric phenotypes frequently show differences between men and women. Although many of these differences are unconfirmed or minor, some appear to be of reasonable robustness and magnitude and are reviewed in this chapter. Sexually dimorphic effects of COMT are usually attributed to transcriptional regulation by oestrogens; however, a careful examination of the literature suggests that additional mechanisms are likely to be at least as important. Here, we review the evidence for a sexually dimorphic influence of COMT upon psychiatric phenotypes and brain function, and discuss potential mechanisms by which this may occur. We conclude that despite the evidence being incomplete, there are accumulating and in places compelling data showing that COMT has markedly sexually dimorphic effects on brain function and its dysfunction in psychiatric disorders. Although oestrogenic regulation of COMT is probably partially responsible for these sex differences, other mechanisms are likely also involved. Since sex differences in the genetic architecture of brain function and psychiatric disorders are the rule not the exception, we anticipate that additional evidence will emerge for sexual dimorphisms, not only in COMT but also in many other autosomal genes.

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Year:  2011        PMID: 21769726     DOI: 10.1007/7854_2010_97

Source DB:  PubMed          Journal:  Curr Top Behav Neurosci        ISSN: 1866-3370


  22 in total

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2.  HIV serostatus differs by catechol-O-methyltransferase Val158Met genotype.

Authors:  Erin E Sundermann; Jeffrey R Bishop; Leah H Rubin; Bradley Aouizerat; Tracey E Wilson; Kathleen M Weber; Mardge Cohen; Elizabeth Golub; Kathryn Anastos; Chenglong Liu; Howard Crystal; Celeste L Pearce; Pauline M Maki
Journal:  AIDS       Date:  2013-07-17       Impact factor: 4.177

3.  Generation and characterization of humanized mice carrying COMT158 Met/Val alleles.

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Journal:  Neuropsychopharmacology       Date:  2014-02-10       Impact factor: 7.853

4.  COMT Val158Met Polymorphism, Cardiometabolic Risk, and Nadir CD4 Synergistically Increase Risk of Neurocognitive Impairment in Men Living With HIV.

Authors:  Rowan Saloner; Maria J Marquine; Erin E Sundermann; Suzi Hong; John Allen McCutchan; Ronald J Ellis; Robert K Heaton; Igor Grant; Mariana Cherner
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5.  Systems pharmacogenomics - gene, disease, drug and placebo interactions: a case study in COMT.

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6.  Genetic markers of dopaminergic transmission predict performance for older males but not females.

Authors:  Kathleen E Hupfeld; David E Vaillancourt; Rachael D Seidler
Journal:  Neurobiol Aging       Date:  2018-02-10       Impact factor: 4.673

7.  Association of abstinence-induced alterations in working memory function and COMT genotype in smokers.

Authors:  Rebecca L Ashare; Jeffrey N Valdez; Kosha Ruparel; Benjamin Albelda; Ryan D Hopson; John R Keefe; James Loughead; Caryn Lerman
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Review 8.  Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

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9.  Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision.

Authors:  Andrey V Bortsov; Luda Diatchenko; Samuel A McLean
Journal:  Neuromolecular Med       Date:  2013-08-21       Impact factor: 3.843

10.  Sex differences in COMT polymorphism effects on prefrontal inhibitory control in adolescence.

Authors:  Thomas P White; Eva Loth; Katya Rubia; Lydia Krabbendam; Robert Whelan; Tobias Banaschewski; Gareth J Barker; Arun L W Bokde; Christian Büchel; Patricia Conrod; Mira Fauth-Bühler; Herta Flor; Vincent Frouin; Jürgen Gallinat; Hugh Garavan; Penny Gowland; Andreas Heinz; Bernd Ittermann; Claire Lawrence; Karl Mann; Marie-Laure Paillère; Frauke Nees; Tomas Paus; Zdenka Pausova; Marcella Rietschel; Trevor Robbins; Michael N Smolka; Sukhwinder S Shergill; Gunter Schumann
Journal:  Neuropsychopharmacology       Date:  2014-05-13       Impact factor: 7.853

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