4.5 Article

Predictors of Achieving Remission among Patients with Psoriatic Arthritis Initiating a Tumor Necrosis Factor Inhibitor

Journal

JOURNAL OF RHEUMATOLOGY
Volume 46, Issue 5, Pages 475-482

Publisher

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.171034

Keywords

PSORIATIC ARTHRITIS; THERAPY RESPONSE; TNF INHIBITORS; OUTCOMES; EPIDEMIOLOGY

Categories

Funding

  1. Corrona Research Foundation
  2. Rheumatology Research Foundation
  3. Corrona
  4. Pfizer
  5. Lilly
  6. AbbVie
  7. Eli Lilly
  8. Amgen
  9. Bristol Myers Squibb
  10. Genentech
  11. Ironwood
  12. [K23 AR063764]
  13. [R01 AR072363]
  14. [NIH-K24AR055989]

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Objective. To examine predictors of remission among patients with psoriatic arthritis (PsA) initiating a tumor necrosis factor (TNF) inhibitor. Methods. Patients with PsA enrolled in the Corrona Registry between 2005 and 2013 were followed from initiation of a TNF inhibitor (TNFi; etanercept, adalimumab, infliximab, certolizumab, or golimumab) to the visit closest to 12 months. Additional inclusion criteria included 3 tender or 3 swollen joints. Outcomes of interest were Clinical Disease Activity Index (CDAI) <= 2.8 (remission), low disease activity (LDA; CDAI <= 10), change in the modified Health Assessment Questionnaire (mHAQ) >= 0.35 and achievement of mHAQ < 0.30. Predictors were measured on or before TNFi initiation. Covariates significant in univariable logistic regression models and <= 5% missing values were included in a multivariable model and removed individually until all remaining variables were significant (p < 0.05). Results. Among 1832 TNFi initiations, 774 initiations (624 patients) met inclusion criteria. Median age at initiation was 52 years [interquartile range (IQR) 44-60], 56% were female, median PsA duration was 4 years (IQR 2-11), and median CDAI at baseline was 20 (IQR 14.5-28). Remission was achieved by 14% and LDA (or remission) by 37%. Achieving remission was positively associated with college education (OR 1.88, 95% CI 1.11-3.19) but negatively associated with female sex (0.62, 95% CI 0.40-0.97), obese body mass index (0.51, 95% CI 0.32-0.81), hypertension (0.55, 95% CI 0.32-0.95), previous biologic use (0.41, 95% CI 0.26-0.65), and baseline pain (0.80 per 10 mm visual analog scale, 95% CI 0.73-0.87). Predictors for LDA, mHAQ < 0.30, and mHAQ change were similar. Conclusion. Few patients with PsA in a US-based registry achieved remission by CDAI criteria. Female sex, obesity, comorbidities, and education influence achievement of remission on a TNFi.

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