4.5 Article

Physical Activity Associates With Lower Systemic Inflammatory Gene Expression in Rheumatoid Arthritis

期刊

JOURNAL OF RHEUMATOLOGY
卷 49, 期 12, 页码 1320-1327

出版社

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.220050

关键词

biomarkers; exercise; inflammation; interferon; interleukin

资金

  1. National Institutes of Health (NIH)/ National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) [R01 AR069616]
  2. NIH/National Heart, Lung, and Blood Institute (NHLBI) [K23HL138461-01A1]
  3. Rheumatology Research Foundation
  4. NIH/NIAMS P30 Center for the Advancement of Precision Medicine in Rheumatology at UCSF [P30AR070155]

向作者/读者索取更多资源

This study found that physical activity is closely associated with the expression of inflammatory genes and signaling pathways in patients with rheumatoid arthritis (RA). After adjusting for sex, age, race, and ethnicity, the most physically active patients showed downregulation of several immune signaling pathways implicated in RA pathogenesis. These results suggest that physical activity may have a protective effect in RA.
Objective. While general population studies have shown inverse associations between physical activity and common inflammatory biomarkers, the effects of physical activity on inflammatory gene expression and signaling pathways in rheumatoid arthritis (RA) remain unknown. We aimed to determine whether physical activity independently associates with expression of inflammatory genes among people with RA. Methods. This was a prospective observational study of adults with RA. Physical activity was measured by quantitative actigraphy over 7 consecutive days, and peripheral blood collected during the same time period was used for RNA sequencing followed by differential gene expression, pathway, and network analyses. Results. Actigraphy and RNA sequencing data were evaluated in 35 patients. The cohort had a mean age of 56 (SD 12) years, and was 91% female, 31% White, 9% Black, 9% Asian, and 40% Hispanic. We found 767 genes differentially expressed (adjusted P < 0.1) between patients in the greatest vs lowest physical activity tertiles, after adjusting for sex, age, race, and ethnicity. The most active patients exhibited dose-dependent downregulation of several immune signaling pathways implicated in RA pathogenesis. These included CD40, STAT3, TREM-1, interleukin (IL)-17A, IL-8, Toll-like receptor, and interferon (IFN) signaling pathways. Upstream cytokine activation state analysis predicted reduced activation of tumor necrosis factor-alpha and IFN in the most active group. In sensitivity analyses, we adjusted for RA disease activity and physical function and found consistent results. Conclusion. Patients with RA who were more physically active had lower expression of immune signaling pathways implicated in RA pathogenesis, even after adjusting for disease activity, suggesting that physical activity may confer a protective effect in RA.

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