Association of Catechol-O-methyltransferase (COMT Val 158 Met) with future risk of cardiovascular disease in depressed individuals - a Swedish population-based cohort study

Aysha Almas, Yvonne Forsell, Vincent Millischer, Jette Möller, Catharina Lavebratt

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8 Citations (Scopus)

Abstract

Background: Catechol-O-methyltransferase (COMT Val 158 Met) has been implicated in both depression and cardiovascular disease. The purpose of this study was to assess if COMT Val 158 Met, which influences the COMT enzyme activity, has an effect on the risk of cardiovascular disease (CVD) in individuals with a history of depression and also to determine if the risk differs depending on gender. Methods: Data from a longitudinal cohort study of mental health among Swedish adults was used. Depression was assessed twice 3 years apart for each participant, in 1998-2001 and 2001-2003. Saliva DNA was contributed by 4349 (41.7%) of the participants and 3525 was successfully genotyped for COMT Val 158 Met. Participants were followed up until December 2014 from the National Patient register with regard to cardiovascular outcomes (hypertensive or ischemic heart disease, and stroke). Results: Those with depression and the high COMT enzyme activity genotype (Val/Val) had almost a three-fold increased risk of later CVD (OR 3.6; 95% CI: 2.0-6.6) compared to those non-depressed carrying the Val/Val allele. This effect on risk for CVD was higher in women compared to men (OR 7.0; 95% CI: 3.0-14.0 versus OR 2.1; 95% CI: 1.0-6.8). Both additive interaction (attributable proportion (AP) = 0.56; 95% CI: 0.24-0.90 and synergy index (SI) = 4.39; 1.0-18.7) and multiplicative interaction (log likelihood test p = 0.1) was present between depression and COMT Val 158 Met in predicting risk of later CVD. Conclusion: High COMT activity genotype Val 158 Met increased the risk of CVD in depressed persons. The risk was higher in women compared to men.

Original languageEnglish
Article number126
JournalBMC Medical Genetics
Volume19
Issue number1
DOIs
Publication statusPublished - 25 Jul 2018

Keywords

  • Depression
  • Gender
  • Genetic variation
  • Myocardial infarction
  • Stroke

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