4.5 Article

Different Rating of Global Rheumatoid Arthritis Disease Activity in Rheumatoid Arthritis Patients With Multiple Morbidities

Journal

ARTHRITIS & RHEUMATOLOGY
Volume 69, Issue 4, Pages 720-727

Publisher

WILEY
DOI: 10.1002/art.39988

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Funding

  1. Bristol- Myers Squibb
  2. Crescendo Bioscience
  3. UCB
  4. Austrian Science Fund [J3476- B23]

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Objective. To quantify differences and determine the factors contributing to the difference in patient global assessment of rheumatoid arthritis (RA) disease activity (PtGA) between RA patients with multiple morbidities (RA-MM) and those with RA only. Methods. We compared the PtGA between RA-MM patients and those with RA only, followed up in a longitudinal cohort (n = 1,040). In analyses performed on RA-MM patients (n = 575) and those with RA only (matched for swollen joint count, tender joint count, evaluator global assessment, and disease duration), the mean difference in PtGA (Delta PtGA) between the 2 groups was assessed. The contribution of patient characteristics to the explained variation of DPtGA in the matched cohort was calculated as semipartial R-2 and summarized as the percentage of the total R-2 in linear regression models. Results. RA-MM patients reported higher (or worse) PtGA, with an increased PtGA associated with more morbidities (P for linear trend < 0.01); this relationship remained significant after adjustment for disease activity, age, and disease duration. After matching 294 RA-MM patients to those with RA only, the pairwise comparison of mean PtGA (on a scale of 0-100 mm) was significantly higher (worse) for RA-MM patients (mean +/- SD 30.5 +/- 24.3) versus those with RA only (25.6 +/- 22.9) (mean DPtGA 4.9 +/- 26.7; P < 0.01 by paired t-test). Variables uniquely contributing to DPtGA were fatigue (18%), pain (17%), and modified Health Assessment Questionnaire scores (9%). Conclusion. In RA patients with multiple morbidities, the perception of RA disease activity as measured by the PtGA might be impacted by the burden of multiple diseases in one individual. RA-MM patients have higher (worse) levels of PtGA scores compared to patients with RA only. The difference in PtGA is mainly explained by differences in fatigue and pain.

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