Depression and anxiety in relation to catechol-O-methyltransferase Val158Met genotype in the general population: the Nord-Trøndelag Health Study (HUNT).
- Authors
- Baekken, Petter M; Skorpen, Frank; Stordal, Eystein; Zwart, John-Anker; Hagen, Knut
- Year
- 2008
- Journal
- BMC psychiatry
- PMID
- 18578865
- DOI
- 10.1186/1471-244X-8-48
- PMCID
- PMC2453123
BACKGROUND: The catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met, which has been linked to anxiety and depression, but previous results are not conclusive. The aim of the present study was to examine the relationship between the Val158Met COMT gene polymorphism and anxiety and depression measured by the Hospital Anxiety and Depression Scale (HADS) in the general adult population. METHODS: In the Nord-Trøndelag Health Study (HUNT) the association between the Val158Met polymorphism and anxiety and depression was evaluated in a random sample of 5531 individuals. Two different cut off scores (> or = 8 and > or = 11) were used to identify cases with anxiety (HADS-A) and depression (HADS-D), whereas controls had HADS-A <8 and HADS-D <8. RESULTS: The COMT genotype distribution was similar between controls and individuals in the groups with anxiety and depression using cut-off scores of > or = 8. When utilizing the alternative cut-off score HADS-D > or = 11, Met/Met genotype and Met allele were less common among men with depression compared to the controls (genotype: p = 0.017, allele: p = 0.006). In the multivariate analysis, adjusting for age and heart disease, depression (HADS-D > or = 11) was less likely among men with the Met/Met genotype than among men with the Val/Val genotype (OR = 0.37, 95% CI = 0.18-0.76). CONCLUSION: In this population-based study, no clear association between the Val158Met polymorphism and depression and anxiety was revealed. The Met/Met genotype was less likely among men with depression defined as HADS-D > or = 11, but this may be an incidental finding.
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| Association of Catechol-O-methyltransferase (COMT Val<sup>158</sup>Met) with future risk of cardiovascular disease in depressed individuals - a Swedish population-based cohort study. | Almas A et al. | — | 2018 | → |
| Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence. | Andersen AM et al. | — | 2017 | → |
| Meta-analysis of the COMT Val158Met polymorphism in major depressive disorder: the role of gender. | Klein M et al. | — | 2016 | → |
| No Association of BDNF, COMT, MAOA, SLC6A3, and SLC6A4 Genes and Depressive Symptoms in a Sample of Healthy Colombian Subjects. | González-Giraldo Y et al. | — | 2015 | → |
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| Association of the catechol-O-methyltransferase val158met polymorphism and anxiety-related traits: a meta-analysis. | Lee LO et al. | — | 2014 | → |
| Interaction effects of the COMT and DRD4 genes with anxiety-related traits on selective attention. | Alfimova M et al. | — | 2014 | → |
| Catechol-O-methyltransferase gene val158met polymorphism and depressive symptoms during early childhood. | Sheikh HI et al. | — | 2013 | → |
| Gender-specific effects of brain-derived neurotrophic factor Val66Met polymorphism and childhood maltreatment on anxiety. | Min JA et al. | — | 2013 | → |
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| Genome-wide association study of comorbid depressive syndrome and alcohol dependence. | Edwards AC et al. | — | 2012 | → |
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| The role of the catechol-O-methyltransferase (COMT) gene in personality and related psychopathological disorders. | Montag C et al. | — | 2012 | → |
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| Association of existing and new candidate genes for anxiety, depression and personality traits in older people. | Luciano M et al. | — | 2010 | → |
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| Enhancing outcomes from major depression: using antidepressant combination therapies with multifunctional pharmacologic mechanisms from the initiation of treatment. | Stahl SM | — | 2010 | → |
| The risk of posttraumatic stress disorder after trauma depends on traumatic load and the catechol-o-methyltransferase Val(158)Met polymorphism. | Kolassa IT et al. | — | 2010 | → |