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

Authors :
George, Steven Z.
Wallace, Margaret R.
Wu, Samuel S.
Moser, Michael W.
Wright, Thomas W.
Farmer, Kevin W.
Borsa, Paul A.
Parr, Jeffrey J.
Greenfield III, Warren H.
Yunfeng Dai
Hua Li
Fillingim, Roger B.
Source :
PAIN. Jan2015, Vol. 156 Issue 1, p148-156. 9p.
Publication Year :
2015

Abstract

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 5 190) to identify high-risk subgroups, and a surgical pain cohort (n 5 150) 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03043959
Volume :
156
Issue :
1
Database :
Academic Search Index
Journal :
PAIN
Publication Type :
Academic Journal
Accession number :
102904502
Full Text :
https://doi.org/10.1016/j.pain.0000000000000012