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Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia

Journal
Arthritis Research & Therapy
ISSN
1478-6354
Date Issued
2007
Author(s)
Vargas Alarcón, Gilberto
Fragoso, José Manuel
Cruz-Robles, David
Vargas, Angélica
Vargas, Alfonso
Lao-Villadóniga, José-Ignacio
García-Fructuoso, Ferrán
Hernández-Sánchez, Fernando
Facultad de Ciencias de la Salud - CampCM  
Springall, Rashidi
Facultad de Ciencias de la Salud - CampCM  
Bojalil, Rafael
Vallejo, Maite
Martínez-Lavín, Manuel
Type
text::journal::journal article
DOI
10.1186/ar2316
URL
https://scripta.up.edu.mx/handle/20.500.12552/2488
Abstract
Autonomic dysfunction is frequent in patients with fibromyalgia (FM). Heart rate variability analyses have demonstrated signs of ongoing sympathetic hyperactivity. Catecholamines are sympathetic neurotransmitters. Catechol-O-methyltransferase (COMT), an enzyme, is the major catecholamine-clearing pathway. There are several single-nucleotide polymorphisms (SNPs) in the COMT gene associated with the different catecholamine-clearing abilities of the COMT enzyme. These SNPs are in linkage disequilibrium and segregate as 'haplotypes'. Healthy females with a particular COMT gene haplotype (ACCG) producing a defective enzyme are more sensitive to painful stimuli. The objective of our study was to define whether women with FM, from two different countries (Mexico and Spain), have the COMT gene haplotypes that have been previously associated with greater sensitivity to pain. All the individuals in the study were female. Fifty-seven Mexican patients and 78 Spanish patients were compared with their respective healthy control groups. All participants filled out the Fibromyalgia Impact Questionnaire (FIQ). Six COMT SNPs (rs2097903, rs6269, rs4633, rs4818, rs4680, and rs165599) were genotyped from peripheral blood DNA. In Spanish patients, there was a significant association between three SNPs (rs6269, rs4818, and rs4680) and the presence of FM when compared with healthy controls. Moreover, in Spanish patients with the 'high pain sensitivity' haplotype (ACCG), the disease, as assessed by the FIQ, was more severe. By contrast, Mexican patients displayed only a weak association between rs6269 and rs165599, and some FIQ subscales. In our group of Spanish patients, there was an association between FM and the COMT haplotype previously associated with high pain sensitivity. This association was not observed in Mexican patients. Studies with a larger sample size are needed in order to verify or amend these preliminary results. © Arthritis Research & Therapy

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