4.7 Article

Intensive lipid lowering in patients with rheumatoid arthritis and previous myocardial infarction: an explorative analysis from the incremental decrease in endpoints through aggressive lipid lowering (IDEAL) trial

Journal

RHEUMATOLOGY
Volume 50, Issue 2, Pages 324-329

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/keq295

Keywords

Rheumatoid arthritis; Secondary prevention; Lipids; Apolipoprotein; Statin; Myocardial infarction

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Funding

  1. Abbott
  2. Roche
  3. Pfizer
  4. Merck-Schering Plough
  5. AstraZeneca
  6. Bristol-Myers Squibb
  7. Schering-Plough
  8. UCB
  9. Wyeth

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Methods. Patients with previous myocardial infarction (MI) were randomly assigned to atorvastatin 80 mg daily or simvastatin 20-40 mg daily and followed for 4.8 years. We focused on changes in lipid levels in the current exploratory analyses and used the composite secondary endpoint in the IDEAL study: any CVD event. Out of the 8888 patients in the IDEAL study, 87 had RA. Results. RA patients had significantly lower baseline levels of total- and low-density lipoprotein (LDL) cholesterol than patients without RA; 4.8 + 1.0 vs 5.1 + 1.0 (P = 0.023) and 2.9 + 0.9 vs 3.1 + 0.9 mmol/l (P = 0.034) for total cholesterol and LDL, respectively. The lipid reductions with either simvastatin or atorvastatin were comparable. Cardiovascular events occurred in 23/87 (26.4%) of the RA patients compared with 2523/8801 (28.7%; P = 0.70) in the general IDEAL population. The occurrence of these events was not related to the duration of RA, age, gender or treatment assignment. Conclusion. Patients with RA and previous MI had comparable lipid-lowering effect and similar rates of cardiovascular events as those without RA, although the RA patients had lower baseline cholesterol levels than patients without RA.

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