4.5 Article

Disease Activity in Rheumatoid Arthritis and the Risk of Cardiovascular Events

期刊

ARTHRITIS & RHEUMATOLOGY
卷 67, 期 6, 页码 1449-1455

出版社

WILEY
DOI: 10.1002/art.39098

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资金

  1. Consortium of Rheumatology Researchers of North America (CORRONA) Research Foundation
  2. Agency for Healthcare Research and Quality [R01-HS-018517]
  3. NIH [AR-064172]
  4. AbbVie
  5. Amgen
  6. AstraZeneca
  7. Genentech
  8. Horizon
  9. Eli Lilly
  10. Novartis
  11. Pfizer
  12. Vertex
  13. UCB
  14. Bristol-Myers Squibb
  15. Lilly
  16. Roche/Genentech
  17. Janssen
  18. CORRONA
  19. Crescendo
  20. University of Massachusetts Medical School
  21. Iroko Pharmaceuticals
  22. Celgene

向作者/读者索取更多资源

Objective. Use of several immunomodulatory agents has been associated with reduced numbers of cardiovascular (CV) events in epidemiologic studies of rheumatoid arthritis (RA). However, it is unknown whether time-averaged disease activity in RA correlates with CV events. Methods.We studied patients with RA whose cases were followed in a longitudinal US-based registry. Time-averaged disease activity was assessed during followup using the area under the curve of the Clinical Disease Activity Index (CDAI), a validated measure of RA disease activity. Age, sex, presence of diabetes mellitus, hypertension, or hyperlipidemia, body mass index, family history of myocardial infarction (MI), use of aspirin or nonsteroidal antiinflammatory drugs (NSAIDs), presence of CV disease, and baseline use of an immunomodulator were assessed at baseline. Cox proportional hazards regression models were examined to determine the risk of a composite CV end point that included MI, stroke, and death from CV causes. Results. A total of 24,989 patients who had been followed up for a median of 2.7 years were included in these analyses. During followup, we observed 534 confirmed CV end points, for an incidence rate of 7.8 per 1,000 person-years (95% confidence interval [95% CI] 6.7-8.9). In models adjusted for variables noted above, a 10-point reduction in the time-averaged CDAI was associated with a 21% reduction in CV risk (95% CI 13-29). These results were robust in subgroup analyses stratified by the presence of CV disease, use of corticosteroids, use of NSAIDs or selective cyclooxygenase 2 inhibitors, and change in RA treatment, as well as when restricted to events adjudicated as definite or probable. Conclusion. Our findings showed that reduced time-averaged disease activity in RA is associated with fewer CV events.

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