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Article

Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility.

Rheumatology international - 1 May 2008

Tander Berna, Gunes Sezgin, Boke Omer, Alayli Gamze, Kara Nurten, Bagci Hasan, Canturk Ferhan

Abstract excerpt

Genetic and environmental factors are thought to play roles in the etiopathology of fibromyalgia syndrome (FMS). The objective of this study was to determine the potential effects of single nucleotide polymorphisms (SNPs) in catechol-O-methyltransferase (COMT) (rs4680) and 5-hydroxytryptamine (serotonin) 2A (5-HT2A) receptor (rs6313 and rs6311) genes on susceptibility to FMS. One hundred seventy-one women (80...

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Share to Catechol O-Methyltransferase
Share to Fibromyalgia
Share to Fibromyalgia and Chronic Fatigue Syndrome Research
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Share to Genetic Predisposition to Disease
Share to Genotype
Share to Polymorphism, Single Nucleotide
Share to Receptor, Serotonin, 5-HT2A

Source

Identifiers

PMID: 18196244
DOI: 10.1007/s00296-008-0525-8

Genes

COMT

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility.PMID 18196244Read ↗

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