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Inflammatory genes and psychological factors predict induced shoulder pain phenotype.

Publication ,  Journal Article
George, SZ; Parr, JJ; Wallace, MR; Wu, SS; Borsa, PA; Dai, Y; Fillingim, RB
Published in: Med Sci Sports Exerc
October 2014

PURPOSE: The pain experience has multiple influences, but little is known about how specific biological and psychological factors interact to influence pain responses. The current study investigated the combined influences of genetic (pro-inflammatory) and psychological factors on several preclinical shoulder pain phenotypes. METHODS: An exercise-induced shoulder injury model was used, and a priori selected genetic (IL1B, TNF/LTA region, and IL6 single nucleotide polymorphisms (SNP)) and psychological (anxiety, depression symptoms, pain catastrophizing, fear of pain, and kinesiophobia) factors were included as the predictors of interest. The phenotypes were pain intensity (5-d average and peak reported on numerical rating scale), upper extremity disability (5-d average and peak reported on the Quick Disabilities of the Arm, Shoulder and Hand instrument), and duration of shoulder pain (d). RESULTS: After controlling for age, sex, and race, the genetic and psychological predictors were entered separately as main effects and interaction terms in regression models for each pain phenotype. Results from the recruited cohort (n = 190) indicated strong statistical evidence for the interactions between 1) TNF/LTA SNP rs2229094 and depression symptoms for average pain intensity and duration and 2) IL1B two SNP diplotype and kinesiophobia for average shoulder pain intensity. Moderate statistical evidence for prediction of additional shoulder pain phenotypes included interactions of kinesiophobia, fear of pain, or depressive symptoms with TNF/LTA rs2229094 and IL1B. CONCLUSIONS: These findings support the combined predictive ability of specific genetic and psychological factors for shoulder pain phenotypes by revealing novel combinations that may merit further investigation in clinical cohorts to determine their involvement in the transition from acute to chronic pain conditions.

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Published In

Med Sci Sports Exerc

DOI

EISSN

1530-0315

Publication Date

October 2014

Volume

46

Issue

10

Start / End Page

1871 / 1881

Location

United States

Related Subject Headings

  • Young Adult
  • Tumor Necrosis Factor-alpha
  • Sport Sciences
  • Shoulder Pain
  • Shoulder Injuries
  • Shoulder
  • Phenotype
  • Middle Aged
  • Male
  • Lymphotoxin-alpha
 

Citation

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George, S. Z., Parr, J. J., Wallace, M. R., Wu, S. S., Borsa, P. A., Dai, Y., & Fillingim, R. B. (2014). Inflammatory genes and psychological factors predict induced shoulder pain phenotype. Med Sci Sports Exerc, 46(10), 1871–1881. https://doi.org/10.1249/MSS.0000000000000328
George, Steven Z., Jeffrey J. Parr, Margaret R. Wallace, Samuel S. Wu, Paul A. Borsa, Yunfeng Dai, and Roger B. Fillingim. “Inflammatory genes and psychological factors predict induced shoulder pain phenotype.Med Sci Sports Exerc 46, no. 10 (October 2014): 1871–81. https://doi.org/10.1249/MSS.0000000000000328.
George SZ, Parr JJ, Wallace MR, Wu SS, Borsa PA, Dai Y, et al. Inflammatory genes and psychological factors predict induced shoulder pain phenotype. Med Sci Sports Exerc. 2014 Oct;46(10):1871–81.
George, Steven Z., et al. “Inflammatory genes and psychological factors predict induced shoulder pain phenotype.Med Sci Sports Exerc, vol. 46, no. 10, Oct. 2014, pp. 1871–81. Pubmed, doi:10.1249/MSS.0000000000000328.
George SZ, Parr JJ, Wallace MR, Wu SS, Borsa PA, Dai Y, Fillingim RB. Inflammatory genes and psychological factors predict induced shoulder pain phenotype. Med Sci Sports Exerc. 2014 Oct;46(10):1871–1881.

Published In

Med Sci Sports Exerc

DOI

EISSN

1530-0315

Publication Date

October 2014

Volume

46

Issue

10

Start / End Page

1871 / 1881

Location

United States

Related Subject Headings

  • Young Adult
  • Tumor Necrosis Factor-alpha
  • Sport Sciences
  • Shoulder Pain
  • Shoulder Injuries
  • Shoulder
  • Phenotype
  • Middle Aged
  • Male
  • Lymphotoxin-alpha