Evidence map›Paper›PMID 24300663›Full record

SynthesisPsychiatric genetics2014

Association of the catechol-O-methyltransferase val158met polymorphism and anxiety-related traits: a meta-analysis.

Lewina O Lee, Carol A Prescott

Abstract readMeta-Analysis
In one paragraph

Synthesis in Psychiatric genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2016
    Pooled it
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  6. Personality andFrontiers in genetics · 2024
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  19. Genotype-Dependent Effects of COMT Inhibition on Cognitive Function in a Highly Specific, Novel Mouse Model of Altered COMT Activity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Lewina O LeeaDepartment of Epidemiology, Boston University School of Public Health bNational Center for Posttraumatic Stress Disorder, Veterans Affairs Boston Healthcare System, Boston, Massachusetts cDepartment of Psychology and Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Carol A Prescott
University of Southern California · USVA Boston Healthcare System · US

Funding

Stress, Coping, Health, & Optimal AgingR01AG032037 · NIA · OREGON STATE UNIVERSITY · PI ALDWIN, CAROLYN M. · 2010 to 2013
$857k
Lifespan outcomes of military serviceR24AG039343 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ALDWIN, CAROLYN M., SPIRO, AVRON · 2010 to 2014
$845k
Anxiety, Stressful Life Events, and Physical Health in Older AdultsF31AG031691 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LEE, LEWINA ONYI · 2007 to 2009
$59k
NIA NIH HHS AG-031691NIA NIH HHS AG-032037NIA NIH HHS AG-039343NIA NIH HHS F31 AG031691NIA NIH HHS R01 AG032037NIA NIH HHS R24 AG039343
6 · The paper itself

Abstract

objectivesThe aims of this study were (i) to examine genotypic association of the catechol-O-methyltransferase (COMT) val158met polymorphism with anxiety-related traits with a meta-analysis; (ii) to examine sex and ethnicity as moderators of the association; and (iii) to evaluate whether the association differed by particular anxiety traits.

methodsAssociation studies of the COMT val158met polymorphism and anxiety traits were identified from the PubMed or PsycInfo databases, conference abstracts, and listserv postings. Exclusion criteria were (a) pediatric samples, (b) exclusively clinical samples, and (c) samples selected for a nonanxiety phenotype. Standardized mean differences in anxiety between genotypes were aggregated to produce mean effect sizes across all available samples, and for subgroups stratified by sex and ethnicity (Whites vs. Asians). Construct-specific analysis was conducted to evaluate the association of COMT with neuroticism, harm avoidance, and behavioral inhibition.

resultsTwenty-seven eligible studies (N=15 979) with available data were identified. Overall findings indicate sex-specific and ethnic-specific effects: valine homozygotes had higher neuroticism than methionine homozygotes in studies of White males [mean effect size(Equation is included in full-text article.)=0.13; 95% CI 0.02, 0.25; P=0.03], and higher harm avoidance in studies of Asian males ((Equation is included in full-text article.)=0.43; 95% CI 0.14, 0.72; P=0.004). No significant associations were found in women and effect sizes were diminished when studies were aggregated across ethnicity or anxiety traits.

conclusionThis meta-analysis provides evidence for sex and ethnic differences in the association of the COMT val158met polymorphism with anxiety traits. Our findings contribute to current knowledge on the relation between prefrontal dopaminergic transmission and anxiety.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdultAnxietyCatechol O-MethyltransferaseEthnicityFemaleGene FrequencyHarm ReductionHumansMaleMiddle AgedPolymorphism, Single NucleotidePublication BiasSocial BehaviorCatechol O-MethyltransferaseCOMT protein, human

Identifiers

PMID24300663
PMCPMC3991696
OpenAlexW2055419972

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.