Literature DB >> 28608575

Association between COMT Val158Met and psychiatric disorders: A comprehensive meta-analysis.

Steven Taylor1.   

Abstract

Catechol-O-methyltransferase (COMT) Val158Met is widely regarded as potentially important for understanding the genetic etiology of many different psychiatric disorders. The present study appears to be the first comprehensive meta-analysis of COMT genetic association studies to cover all psychiatric disorders for which there were available data, published in any language, and with an emphasis on investigating disorder subtypes (defined clinically or by demographic or other variables). Studies were included if they reported one or more datasets (i.e., some studies examined more than one clinical group) in which there were sufficient information to compute effect sizes. A total of 363 datasets were included, consisting of 56,998 cases and 74,668 healthy controls from case control studies, and 2,547 trios from family based studies. Fifteen disorders were included. Attention-deficit hyperactivity disorder and panic disorder were associated with the Val allele for Caucasian samples. Substance-use disorder, defined by DSM-IV criteria, was associated with the Val allele for Asian samples. Bipolar disorder was associated with the Met allele in Asian samples. Obsessive-compulsive disorder tended to be associated with the Met allele only for males. There was suggestive evidence that the Met allele is associated with an earlier age of onset of schizophrenia. Results suggest pleiotropy and underscore the importance of examining subgroups-defined by variables such as age of onset, sex, ethnicity, and diagnostic system-rather than examining disorders as monolithic constructs.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  COMT; Val158Met; catechol-O-methyltransferase; psychiatric genetics; rs4680

Mesh:

Substances:

Year:  2017        PMID: 28608575     DOI: 10.1002/ajmg.b.32556

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  18 in total

1.  Selective role for the COMT polymorphism in a trans-diagnostic compulsivity phenotype.

Authors:  Samuel R Chamberlain; Jon E Grant
Journal:  Psychol Med       Date:  2018-08-24       Impact factor: 7.723

2.  Systems pharmacogenomics - gene, disease, drug and placebo interactions: a case study in COMT.

Authors:  Kathryn T Hall; Joseph Loscalzo; Ted J Kaptchuk
Journal:  Pharmacogenomics       Date:  2019-05       Impact factor: 2.533

Review 3.  Insights into S-adenosyl-l-methionine (SAM)-dependent methyltransferase related diseases and genetic polymorphisms.

Authors:  Jiaojiao Li; Chunxiao Sun; Wenwen Cai; Jing Li; Barry P Rosen; Jian Chen
Journal:  Mutat Res Rev Mutat Res       Date:  2021-10-07       Impact factor: 7.015

4.  Analysis of COMT Val158Met polymorphisms and methylation in Chinese male schizophrenia patients with homicidal behavior.

Authors:  Yikai Hu; Chenghu Li; Yangfan Wang; Qinhan Li; Yidong Liu; Shengde Liao; Peiqing Cao; Hongmei Xu
Journal:  Int J Legal Med       Date:  2018-02-17       Impact factor: 2.686

5.  Catechol-O-methyltransferase Val158Met Genotype and Early-Life Family Adversity Interactively Affect Attention-Deficit Hyperactivity Symptoms Across Childhood.

Authors:  Eyal Abraham; Marc A Scott; Clancy Blair
Journal:  Front Genet       Date:  2020-07-10       Impact factor: 4.772

6.  Relationships of Cerebrospinal Fluid Alzheimer's Disease Biomarkers and COMT, DBH, and MAOB Single Nucleotide Polymorphisms.

Authors:  Mirjana Babić Leko; Matea Nikolac Perković; Nataša Klepac; Dubravka Švob Štrac; Fran Borovečki; Nela Pivac; Patrick R Hof; Goran Šimić
Journal:  J Alzheimers Dis       Date:  2020       Impact factor: 4.472

Review 7.  Pharmacogenomic Characterization in Bipolar Spectrum Disorders.

Authors:  Stefano Fortinguerra; Vincenzo Sorrenti; Pietro Giusti; Morena Zusso; Alessandro Buriani
Journal:  Pharmaceutics       Date:  2019-12-21       Impact factor: 6.321

8.  COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents.

Authors:  Sabina K Millenet; Frauke Nees; Stefan Heintz; Christiane Bach; Josef Frank; Sabine Vollstädt-Klein; Arun Bokde; Uli Bromberg; Christian Büchel; Erin B Quinlan; Sylvane Desrivières; Juliane Fröhner; Herta Flor; Vincent Frouin; Hugh Garavan; Penny Gowland; Andreas Heinz; Bernd Ittermann; Herve Lemaire; Jean-Luc Martinot; Marie-Laure P Martinot; Dimitri O Papadoulos; Tomáš Paus; Luise Poustka; Marcella Rietschel; Michael N Smolka; Henrik Walter; Rob Whelan; Gunter Schumann; Tobias Banaschewski; Sarah Hohmann
Journal:  Front Genet       Date:  2018-07-31       Impact factor: 4.599

9.  Association between COMT gene rs165599 SNP and schizophrenia: A meta-analysis of case-control studies.

Authors:  Harika Gozde Gozukara Bag
Journal:  Mol Genet Genomic Med       Date:  2018-08-30       Impact factor: 2.183

10.  Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia.

Authors:  Marina Sagud; Lucija Tudor; Suzana Uzun; Matea Nikolac Perkovic; Maja Zivkovic; Marcela Konjevod; Oliver Kozumplik; Bjanka Vuksan Cusa; Dubravka Svob Strac; Iva Rados; Ninoslav Mimica; Alma Mihaljevic Peles; Gordana Nedic Erjavec; Nela Pivac
Journal:  Front Pharmacol       Date:  2018-07-03       Impact factor: 5.810

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