No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study

被引:48
作者
Hagen, Knut [1 ]
Pettersen, Elin
Stovner, Lars Jacob
Skorpen, Frank
Zwart, John-Anker
机构
[1] Norwegian Univ Sci & Technol, Dept Clin Neurosci, N-7034 Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Fac Med, Dept Lab Med, N-7034 Trondheim, Norway
[3] Norwegian Natl Headache Ctr, Neurol Sect, Trondheim, Norway
[4] St Olavs Hosp, Natl Ctr Spinal Disorders, Trondheim, Norway
关键词
D O I
10.1186/1471-2474-7-40
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: The Catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met, that has been found to influence human pain perception. In one study fibromyalgia was less likely among those with Val/Val genotype. Methods: In the 1995 - 97 Nord-Trondelag Health Study (HUNT), the association between Val/ Met polymorphism at the COMT gene and chronic musculoskeletal complaints (MSCs) was evaluated in a random sample of 3017 individuals. Results: The distribution of the COMT Val158Met genotypes and alleles were similar between controls and the twelve different chronic MSCs groups. Even when the Met/Met and Val/ Met genotypes were pooled, the distribution of the Val/ Val genotype and other genotypes were similar between controls and the chronic MSCs groups. Conclusion: In this population-based study, no significant association was found between Val/ Met polymorphism at the COMT gene and chronic MSCs.
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