Facial pain with localized and widespread manifestations: separate pathways of vulnerability.

Journal Article (Journal Article)

Human association studies of common genetic polymorphisms have identified many loci that are associated with risk of complex diseases, although individual loci typically have small effects. However, by envisaging genetic associations in terms of cellular pathways, rather than any specific polymorphism, combined effects of many biologically relevant alleles can be detected. The effects are likely to be most apparent in investigations of phenotypically homogenous subtypes of complex diseases. We report findings from a case-control, genetic association study of relationships between 2925 single nucleotide polymorphisms (SNPs) and 2 subtypes of a commonly occurring chronic facial pain condition, temporomandibular disorder (TMD): 1) localized TMD and 2) TMD with widespread pain. When compared to healthy controls, cases with localized TMD differed in allelic frequency of SNPs that mapped to a serotonergic receptor pathway (P=0.0012), while cases of TMD with widespread pain differed in allelic frequency of SNPs that mapped to a T-cell receptor pathway (P=0.0014). A risk index representing combined effects of 6 SNPs from the serotonergic pathway was associated with greater odds of localized TMD (odds ratio 2.7, P=1.3 E-09), and the result was reproduced in a replication case-control cohort study of 639 people (odds ratio 1.6, P=0.014). A risk index representing combined effects of 8 SNPs from the T-cell receptor pathway was associated with greater odds of TMD with widespread pain (P=1.9 E-08), although the result was not significant in the replication cohort. These findings illustrate potential for clinical classification of chronic pain based on distinct molecular profiles and genetic background.

Full Text

Duke Authors

Cited Authors

  • Slade, GD; Smith, SB; Zaykin, DV; Tchivileva, IE; Gibson, DG; Yuryev, A; Mazo, I; Bair, E; Fillingim, R; Ohrbach, R; Greenspan, J; Maixner, W; Diatchenko, L

Published Date

  • November 2013

Published In

Volume / Issue

  • 154 / 11

Start / End Page

  • 2335 - 2343

PubMed ID

  • 23867732

Pubmed Central ID

  • PMC3808468

Electronic International Standard Serial Number (EISSN)

  • 1872-6623

Digital Object Identifier (DOI)

  • 10.1016/j.pain.2013.07.009


  • eng

Conference Location

  • United States