Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shahid Sadoughi University of Medical Sciences

Association of catechol-O-methyltranferase 472G>A (Val158Met) polymorphism with susceptibility to fibromyalgia syndrome

(2020) Association of catechol-O-methyltranferase 472G>A (Val158Met) polymorphism with susceptibility to fibromyalgia syndrome. Journal of Orthopaedics. pp. 257-260. ISSN 0972-978X (Print) 0972-978X (Electronic) 0972-978X (Linking)

Full text not available from this repository.

Official URL: https://www.ncbi.nlm.nih.gov/pubmed/32127730

Abstract

BACKGROUND: Several lines of research have suggested that the 472G > A (Val158Met) polymorphism at Catechol-O-methyltranferase (COMT) gene is implicated in the pathophysiology of FMS. Here, we have evaluated the association of COMT 472G > A polymorphism with risk of FMS. METHODS: In this study 250 patients with FMS and 250 healthy controls were evaluated for COMT 472G > A polymorphism by RFLP-PCR assay. RESULTS: There were no significant differences in the allele and genotype frequencies of COMT 472G > A polymorphism between FMS cases and healthy controls. CONCLUSIONS: Our results suggested that the COMT 472G > A polymorphism may not be risk factor for development of FMS.

Item Type: Article
Keywords: Catechol-O-Methyltransferase Fibromyalgia Pain Polymorphism
Page Range: pp. 257-260
Journal or Publication Title: Journal of Orthopaedics
Volume: 20
Identification Number: https://doi.org/10.1016/j.jor.2020.01.013
ISSN: 0972-978X (Print) 0972-978X (Electronic) 0972-978X (Linking)
Depositing User: Mr mahdi sharifi
URI: http://eprints.ssu.ac.ir/id/eprint/31058

Actions (login required)

View Item View Item