rs4680, COMT;MIR4761

N. diseases: 249
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE This meta-analysis identified an association between fibromyalgia risk and the COMT Val158Met polymorphism as well as the FIQ score in fibromyalgia patients. 24951880 2015
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE The genotype frequencies of Val158Met polymorphism showed a small difference between FMS patients and healthy controls (p = 0.047), however, the Met/Met genotype was significantly higher in FMS patients than healthy controls (p = 0.016). 24762091 2014
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE These results provide initial evidence of a link between Val158Met polymorphism and dysfunctions in the SNS and humoral immune system in women with FMS. 24503977 2014
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE According with previous research, our findings revealed that haplotypes of the COMT gene and genotypes of the Val158Met polymorphism play a key role on pain sensitivity in FM patients. 22528689 2013
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE This study suggests that the Val158Met COMT polymorphism modulated some psychological variables but not pressure pain sensitivity in FMS because women with FMS carrying the Met/Met genotype exhibit higher disability, depression, and anxiety than but similar PPTs to those with Val/Met and Val/Val genotypes. 23025981 2012
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE The meta-analyses showed that fibromyalgia or chronic widespread pain is the only type of chronic pain that could be associated with the COMT single nucleotide polymorphism rs4680 (Val158Met). 22722321 2012
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE These results suggest that SNPs rs4680 and rs4818 of the COMT gene may be associated with fibromyalgia and pain sensitivity in FS Brazilian patients. 21120493 2012
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE The findings provide multimeasure and multimethod support for genetic moderation of a maladaptive coping and pain process and suggest that genetic variation in the val(158)met polymorphism may affect fibromyalgia pain through pathways of pain-related cognition. 21130573 2011
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE We observed an association between FM and the COMT val(158) met polymorphism in a dose response effect of the COMT genotype and the number of pressure points reported. 20074440 2010
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE We sought to investigate the relationships between catecholamine-related polymorphisms [dopamine-D(3) receptor (DRD3) Ser9Gly and catechol-O-methyltransferase (COMT) Val158Met] and thermal pain measures in healthy subjects and FM patients. 19464960 2009
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE 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. 18196244 2008
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.100 GeneticVariation BEFREE 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. 17961261 2007