Biopsychosocial influence on shoulder pain: risk subgroups translated across preclinical and clinical prospective cohorts.

Journal Article (Journal Article)

Tailored treatment based on individual risk factors is an area with promise to improve options for pain relief. Musculoskeletal pain has a biopsychosocial nature, and multiple factors should be considered when determining risk for chronic pain. This study investigated whether subgroups comprised genetic and psychological factors predicted outcomes in preclinical and clinical models of shoulder pain. Classification and regression tree analysis was performed for an exercise-induced shoulder injury cohort (n = 190) to identify high-risk subgroups, and a surgical pain cohort (n = 150) was used for risk validation. Questionnaires for fear of pain and pain catastrophizing were administered before injury and preoperatively. DNA collected from saliva was genotyped for a priori selected genes involved with pain modulation (COMT and AVPR1A) and inflammation (IL1B and TNF/LTA). Recovery was operationalized as a brief pain inventory rating of 0/10 for current pain intensity and <2/10 for worst pain intensity. Follow-up for the preclinical cohort was in daily increments, whereas follow-up for the clinical cohort was at 3, 6, and 12 months postoperatively. Risk subgroups comprised the COMT high pain sensitivity variant and either pain catastrophizing or fear of pain were predictive of heightened shoulder pain responses in the preclinical model. Further analysis in the clinical model identified the COMT high pain sensitivity variant and pain catastrophizing subgroup as the better predictor. Future studies will determine whether these findings can be replicated in other anatomical regions and whether personalized medicine strategies can be developed for this risk subgroup.

Full Text

Duke Authors

Cited Authors

  • George, SZ; Wallace, MR; Wu, SS; Moser, MW; Wright, TW; Farmer, KW; Borsa, PA; Parr, JJ; Greenfield, WH; Dai, Y; Li, H; Fillingim, RB

Published Date

  • January 2015

Published In

Volume / Issue

  • 156 / 1

Start / End Page

  • 148 - 156

PubMed ID

  • 25599310

Pubmed Central ID

  • PMC4801181

Electronic International Standard Serial Number (EISSN)

  • 1872-6623

Digital Object Identifier (DOI)

  • 10.1016/j.pain.0000000000000012


  • eng

Conference Location

  • United States