4.4 Article

Greater Likelihood of Remission in Rheumatoid Arthritis Patients Treated Earlier in the Disease Course: Results From the Consortium of Rheumatology Researchers of North America Registry

Journal

ARTHRITIS CARE & RESEARCH
Volume 63, Issue 6, Pages 856-864

Publisher

WILEY
DOI: 10.1002/acr.20452

Keywords

-

Categories

Funding

  1. Abbott
  2. Amgen
  3. BMS
  4. Centocor
  5. Genentech
  6. Lilly
  7. Roche
  8. NIH [K23-AR053856, K23-AR054412]
  9. Arthritis Foundation
  10. Bristol-Myers Squibb
  11. Actelion
  12. Biogen Idec
  13. Gilead
  14. GSK
  15. NI
  16. Nitec
  17. Novartis
  18. Pfizer
  19. UCB
  20. Centocor-Ortho Biotech
  21. HGS
  22. CORRONA
  23. University of Massachusetts

Ask authors/readers for more resources

Objective. To examine whether disease duration is an independent predictor of achieving remission in rheumatoid arthritis (RA) patients initiating therapy. Methods. RA patients in the Consortium of Rheumatology Researchers of North America registry newly prescribed a nonbiologic disease-modifying antirheumatic drug (DMARD) or anti tumor necrosis factor (anti-TNF) with at least one followup visit were identified. Achievement of remission was defined using the Clinical Disease Activity Index (CDAI; score <= 2.8) and 28-joint Disease Activity Score (DAS28; score <2.6) at any followup visit within one year; sustained remission was defined as remission during any two successive visits. Likelihood of remission was examined through logistic regression based on 5-year increments of disease duration, adjusting for baseline covariates. Results. Among the 1,646 nonbiologic DMARD initiators, CDAI remission occurred in 21.3% of those with <= 5 years of disease duration, 19.6% with 6-10 years, and 13.5% with >= 11 years (P < 0.001); sustained remission occurred in 10.2%, 8.8%, and 2.5%, respectively (P < 0.001). Results were similar among the 3,179 anti-TNF initiators (CDAI remission in 22.3%, 17.7%, and 12.8%, respectively [P < 0.001]; CDAI sustained remission in 9.7%, 9.5%, and 4.2%, respectively [P < 0.001]). DAS28 results were similar in both groups. In adjusted analyses, an increase of disease duration by 5 years was associated with a reduced likelihood of CDAI remission in nonbiologic DMARD (odds ratio [OR] 0.91, 95% confidence interval [95% CI] 0.83-0.99) and anti-TNF initiators (OR 0.88, 95% CI 0.83-0.94). A similar result was seen for sustained remission using the CDAI (nonbiologic DMARD: OR 0.61, 95% CI 0.48-0.76; anti-TNF: OR 0.85, 95% CI 0.75-0.97). Conclusion. Earlier treatment was associated with a greater likelihood of remission.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available