4.7 Article

Incidence and predictors of secondary fibromyalgia in an early arthritis cohort

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 72, Issue 6, Pages 949-954

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2012-201506

Keywords

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Categories

Funding

  1. NIH [AR 057578, AR 055989]
  2. Amgen Canada Inc.
  3. Pfizer Canada Inc.
  4. Hoffmann-La Roche Ltd.
  5. United Chemicals of Belgium (UCB) Canada Inc.
  6. Bristol-Myers Squibb Canada Co.
  7. Abbott Laboratories Ltd.
  8. Janssen Biotech Inc. (Johnson Johnson Inc.)
  9. Forest
  10. Merck Canada
  11. Novartis
  12. Amgen
  13. Warner-Chilcott
  14. Janssen
  15. Abbott
  16. Institut de rheumatologie de Montreal
  17. UCB
  18. AstraZeneca
  19. BMS
  20. Roche
  21. Johnson and Johnson
  22. Pfizer
  23. Actelion
  24. Glaxo Smith Kline
  25. Centocor
  26. Genzyme
  27. Merck
  28. Lilly

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Objectives Secondary fibromyalgia (FM) is common among patients with inflammatory arthritis, but little is known about its incidence and the factors leading to its development. The authors examined the incidence of secondary FM in an early inflammatory arthritis cohort, and assessed the association between pain, inflammation, psychosocial variables and the clinical diagnosis of FM. Methods Data from 1487 patients in the Canadian Early Arthritis Cohort, a prospective, observational Canadian cohort of early inflammatory arthritis patients were analysed. Diagnoses of FM were determined by rheumatologists. Incidence rates were calculated, and Cox regression models were used to determine HRs for FM risk. Results The cumulative incidence rate was 6.77 (95% CI 5.19 to 8.64) per 100 person-years during the first 12 months after inflammatory arthritis diagnosis, and decreased to 3.58 (95% CI 1.86 to 6.17) per 100 person-years 12-24 months after arthritis diagnosis. Pain severity (HR 2.01, 95% CI 1.17 to 3.46) and poor mental health (HR 1.99, 95% CI 1.09 to 3.62) predicted FM risk. Citrullinated peptide positivity (HR 0.48, 95% CI 0.26 to 0.88) was associated with decreased FM risk. Serum inflammatory markers and swollen joint count were not significantly associated with FM risk. Conclusions The incidence of FM was from 3.58 to 6.77 cases per 100 person-years, and was highest during the first 12 months after diagnosis of inflammatory arthritis. Although inflammation was not associated with the clinical diagnosis of FM, pain severity and poor mental health were associated with the clinical diagnosis of FM. Seropositivity was inversely associated with the clinical diagnosis of FM.

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