4.7 Article

Biomarker-related risk for myocardial infarction and serious infections in patients with rheumatoid arthritis: a population-based study

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 77, Issue 3, Pages 386-392

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2017-211727

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Funding

  1. Crescendo Bioscience, a Myriad Genetics Company
  2. Patient-Centered Outcomes Research Institute (PCORI)

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Background R heumatoid arthritis (RA) disease activity and associated systemic inflammation has been associated with serious infection (SIEs), myocardial infarction (MI) and coronary heart disease (CHD) events based on a few registry studies or clinical trials. There are few data from large-scale population-based studies given feasibility challenges in conducting such investigations. Methods Multibiomarker disease activity (MBDA) test scores (n= 77 641) were linked to Medicare for US patients with RA. Outcomes of interest were hospitalised pneumonia/sepsis (SIE), MI and a composite CHD outcome. The MBDA score ranges from 1 to 100 and was analysed as time-varying. Cox proportional hazards models evaluated the association between MBDA score and SIEs, MI and CHD events, controlling for potential confounders. A sensitivity analysis excluded C reactive protein (CRP) from the MBDA score. Results T here were 17 433 and 16 796 patients eligible for the SIE and MI/CHD analyses, respectively. Mean (SD) age was 69 (11) years, 79% were women, 81% were white and 38% were disabled. Over 16 424 person-years of follow-up, there were 452 SIE events, 132 MIs and 181 CHD events. Higher MBDA scores were associated with SIEs (HR= 1.32, 95% CI 1.23 to 1.41 per 10 unit MBDA score change). For MI/CHD events, a threshold effect was present; higher disease activity by MBDA score was associated with increased MI (HR= 1.52, 95% CI 0.92 to 2.49) and CHD rates (HR= 1.54, 95% CI 1.01 to 2.34, comparing scores = 30 vs < 30). Analyses of the MBDA score without CRP yielded similar results. Conclusion Higher MBDA scores were associated with hospitalised infection, MI and CHD events in a large, predominantly older, US RA population.

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