Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.
Ontology highlight
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 hap
SUBMITTER: Vargas-Alarcon G
PROVIDER: S-EPMC2212567 | biostudies-literature | 2007
REPOSITORIES: biostudies-literature
ACCESS DATA