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The impact of the Catechol-O-methyltransferase Val158Met polymorphism on survival in the general population – the HUNT study

Knut Hagen12*, Lars J Stovner12, Frank Skorpen3, Elin Pettersen3 and John-Anker Zwart124

Author Affiliations

1 Department of Clinical Neuroscience, Faculty of medicine, Norwegian University of Science and Technology, Trondheim, Norway

2 Norwegian National Headache Centre, Section of Neurology, St. Olavs Hospital, Trondheim, Norway

3 Department of Laboratory Medicine, Children's and Women's health, Faculty of medicine, Norwegian University of Science and Technology, Trondheim, Norway

4 National Centre for Spinal Disorders, St. Olavs Hospital, Trondheim, Norway

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BMC Medical Genetics 2007, 8:34  doi:10.1186/1471-2350-8-34

Published: 19 June 2007



The catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met which has been related to common diseases like cancer, psychiatric illness and myocardial infarction. Whether the Val158Met polymorphism is associated with survival has not been evaluated in the general population. The aim of this prospective study was to evaluate the impact of codon 158 COMT gene polymorphism on survival in a population-based cohort.


The sample comprised 2979 non-diabetic individuals who participated in the Nord-Trøndelag Health Study (HUNT) in the period 1995–97. The subjects were followed up with respect to mortality throughout year 2004.


212 men and 183 women died during the follow up. No association between codon 158 COMT gene polymorphism and survival was found. The unadjusted relative risk of death by non-ischemic heart diseases with Met/Met or Met/Val genotypes was 3.27 (95% confidence interval, 1.19–9.00) compared to Val/Val genotype. When we adjusted for age, gender, smoking, coffee intake and body mass index the relative risk decreased to 2.89 (95% confidence interval, 1.04–8.00).


During 10 year of follow-up, the Val158Met polymorphism had no impact on survival in a general population. Difference in mortality rates from non-ischemic heart diseases may be incidental and should be evaluated in other studies.