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Systematic Review and Meta-Analysis: Anti-Tumor Necrosis Factor α Therapy and Cardiovascular Events in Rheumatoid Arthritis

Journal

ARTHRITIS CARE & RESEARCH
Volume 63, Issue 4, Pages 522-529

Publisher

WILEY
DOI: 10.1002/acr.20371

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Funding

  1. UCBeyond-The Arthritis Society-Canadian Rheumatology Association
  2. Canadian Institutes of Health Research
  3. Government of Canada Research Chair in Health Services Research
  4. Alberta Heritage Foundation for Medical Research
  5. Abbott
  6. Amgen/Wyeth

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Objective. Control of rheumatoid arthritis (RA) may reduce the risk of cardiovascular events. We sought to systematically assess the association between anti-tumor necrosis factor (anti-TNF alpha) therapy in RA and cardiovascular event rates. Methods. Observational cohorts and randomized controlled trials (RCTs) reporting on cardiovascular events (all events, myocardial infarction [MI], congestive heart failure, and cerebrovascular accident [CVA]) in RA patients treated with anti-TNF alpha therapy compared to traditional disease-modifying antirheumatic drugs were identified from a search of PubMed (1950 to November 2009), EMBase (1980 to November 2009), and conference abstracts. Relative risks (RRs) or hazard ratios and 95% confidence intervals (95% CIs) were extracted. If the incidence was reported, additional data were extracted to calculate an incidence density ratio and its variance. Results. The systematic review and meta-analysis include 16 and 11 publications, respectively. In cohort studies, anti-TNF alpha therapy was associated with a reduced risk for all cardiovascular events (pooled adjusted RR 0.46; 95% CI 0.28, 0.77), MI (pooled adjusted RR 0.81; 95% CI 0.68, 0.96), and CVA (pooled adjusted RR 0.69; 95% CI 0.53, 0.89). Meta-analysis of RCTs also produced a point estimate indicating lower risk of cardiovascular events, but this was not statistically significant (pooled RR 0.85; 95% CI 0.28, 2.59). Conclusion. Anti-TNF alpha therapy is associated with a reduced risk of all cardiovascular events, MI, and CVA in observational cohorts. There was heterogeneity among cohort studies and possible publication bias. The point estimate of the effect from RCTs is underpowered with wide 95% CIs, and cardiovascular events were secondary outcomes, but RCTs also demonstrated a trend toward decreased risk.

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