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

نویسندگان

  • Knut Hagen
  • Elin Pettersen
  • Lars Jacob Stovner
  • Frank Skorpen
  • John-Anker Zwart
چکیده

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-Trøndelag 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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عنوان ژورنال:
  • BMC Musculoskeletal Disorders

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2006