Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/16815
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Type: Journal article
Title: Genetic basis for individual variations in pain perception and the development of a chronic pain condition
Author: Diatchenko, L.
Slade, G.
Nackley Neely, A.
Bhalang, K.
Sigurdsson, A.
Belfer, I.
Goldman, D.
Xu, K.
Shabalina, S.
Shagin, D.
Max, M.
Makarov, S.
Maixner, W.
Citation: Human Molecular Genetics, 2005; 14(1):135-143
Publisher: Oxford Univ Press
Issue Date: 2005
ISSN: 0964-6906
1460-2083
Statement of
Responsibility: 
Luda Diatchenko, Gary D. Slade, Andrea G. Nackley, Konakporn Bhalang, Asgeir Sigurdsson, Inna Belfer, David Goldman, Ke Xu, Svetlana A. Shabalina, Dmitry Shagin, Mitchell B. Max, Sergei S. Makarov, and William Maixner
Abstract: Pain sensitivity varies substantially among humans. A significant part of the human population develops chronic pain conditions that are characterized by heightened pain sensitivity. We identified three genetic variants (haplotypes) of the gene encoding catecholamine-O-methyltransferase (COMT) that we designated as low pain sensitivity (LPS), average pain sensitivity (APS) and high pain sensitivity (HPS). We show that these haplotypes encompass 96% of the human population, and five combinations of these haplotypes are strongly associated (P 5 0.0004) with variation in the sensitivity to experimental pain. The presence of even a single LPS haplotype diminishes, by as much as 2.3 times, the risk of developing myogenous temporomandibular joint disorder (TMD), a common musculoskeletal pain condition. The LPS haplotype produces much higher levels of COMT enzymatic activity when compared with the APS or HPS haplotypes. Inhibition of COMT in the rat results in a profound increase in pain sensitivity. Thus, COMT activity substantially influences pain sensitivity, and the three major haplotypes determine COMT activity in humans that inversely correlates with pain sensitivity and the risk of developing TMD.
Keywords: Animals
Humans
Rats
Temporomandibular Joint Disorders
Pain
Chronic Disease
Catechol O-Methyltransferase
Risk Factors
Haplotypes
Adolescent
Adult
Female
Description: Copyright © 2005 Oxford University Press
DOI: 10.1093/hmg/ddi013
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