4.7 Article

Comorbidities are associated with poorer outcomes in community patients with rheumatoid arthritis

Journal

RHEUMATOLOGY
Volume 52, Issue 10, Pages 1809-1817

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/ket224

Keywords

comorbidities; rheumatoid arthritis; age; remission

Categories

Funding

  1. ACR/REF/ASP Junior Career Development Award in Geriatric Medicine
  2. National Institute of Arthritis and Musculoskeletal and Skin Diseases, part of the National Institutes of Health [NIAMS K23 AR057818-02]
  3. Scleroderma Foundation
  4. National Institutes of Health Award [NIAMS K23 AR053858-04]
  5. Abbvie
  6. Actelion
  7. Amgen
  8. BMS
  9. Gilead
  10. GSK
  11. NIH
  12. Novartis
  13. Pfizer
  14. Roche/Genentech
  15. UCB
  16. Biogen Idec
  17. Janssen
  18. Genetech

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Objective. To evaluate the impact of comorbidities on achieving remission by examining changes in the clinical disease activity index (CDAI) in RA patients in the community-based Consortium of Rheumatology Researchers of North America (CORRONA) registry. Methods. A subcohort of 1548 RA subjects with varying disease duration met the following inclusion criteria: started a DMARD/biologic agent, continued therapy 53 months, CDAI 52.8 at study entry and followed longitudinally from baseline to follow-up (mean time 7.46 months). Patients reported comorbidities according to a standardized list of 33 conditions. Entry characteristics were compared across age categories using one-way analysis of variance. Linear and logistic regression models were constructed to assess characteristics [e. g. age, disease duration, number of previous DMARDs/biologics, baseline modified health assessment questionnaire (MHAQ), baseline CDAI and number of comorbidities] associated with primary outcomes: change in CDAI (baseline to follow-up) and CDAI remission (yes/no). Results. Although disease activity measures at entry were similar across age categories, older patients had more comorbidities, less improvement in CDAI/MHAQ and were less likely to attain remission at follow-up. However, after adjusting covariates an increasing number of patient-reported comorbidities and higher baseline CDAI (but not age) were consistently and independently associated with a lower likelihood of clinical improvement or remission (P<0.001). Conclusion. In this observational cohort of community RA patients an increasing number of patients reported comorbidities, independently correlated with less CDAI improvement over time. These results reaffirm that comorbidities may be an important factor in consideration of treat-to-target recommendations and aid in understanding achievable RA therapeutic goals.

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