Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE In the present study, we used functional Magnetic Resonance Imaging (fMRI) to investigate the brain response to heat pain stimuli in 54 subjects genotyped for the common COMT val158met polymorphism (val/val = n 22, val/met = n 20, met/met = n 12). 22132136

2011

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE However, genetic effects (COMT Val(158)Met and BDNF Val(66)Met) on experimental pain were moderated by the presence of chronic pain. 21049025

2010

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE More generally, apart from one report that focused on pain-induced opioid release, this is the first functional neuroimaging study showing an effect of the COMT val158met polymorphism on cerebral pain processing. 20509977

2010

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE COMT Val158Met and thermal pain measures were not related. 19464960

2009

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Genetics-based personalized approaches to pain management have received a setback because of the nonreproducibility of functional genetic associations such as the pain-modulatory effect of the catechol-O-methyl transferase (COMT) gene 472G>A single-nucleotide polymorphism. 18548001

2009

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Increased sensitivity to thermal pain following a single opiate dose is influenced by the COMT val(158)met polymorphism. 19547755

2009

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Three common haplotypes of the human COMT gene, divergent in two synonymous and one nonsynonymous (val(158)met) position, designated as low (LPS), average (APS), and high pain sensitive (HPS), are associated with experimental pain sensitivity and risk of developing chronic musculoskeletal pain conditions. 19365560

2009

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE It is shown that a polymorphism in the COMT gene, Rs4680 (Val158Met), influence pain sensitivity in human experimental pain and the efficacy for morphine in cancer pain treatment. 19094200

2008

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE This suggests that the val(1</span>58)met SNP plays a primary role in variation in temporal summation of pai</span>n, but that other SNPs of the COMT haplotype exert a greater influence on resting nociceptive sensitivity. 16837133

2006

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The Catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met, that has been found to influence human pain perception. 16674809

2006

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met, that has been found to influence human pain perception, and one study has found that migraine was less likely among those with the Val/Val polymorphism. 16688411

2006

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE A single nucleotide polymorphism (Val158Met) of COMT leads to a three to four fold reduction in the activity of the enzyme and has been associated to modifications in the response to a pain stressor. 15862471

2005

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The Val158Met polymorphism affects pain perception, and subjects with the Met/Met genotype have the most pronounced response to experimental pain. 15927391

2005

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The COMT val158met polymorphism thus influences the human experience of pain and may underlie interindividual differences in the adaptation and responses to pain and other stressful stimuli. 12595695

2003