Biomedicines (Feb 2023)

Predictors of DAPSA Response in Psoriatic Arthritis Patients Treated with Apremilast in a Retrospective Observational Multi-Centric Study

  • Andrea Becciolini,
  • Simone Parisi,
  • Patrizia Del Medico,
  • Antonella Farina,
  • Elisa Visalli,
  • Aldo Biagio Molica Colella,
  • Federica Lumetti,
  • Rosalba Caccavale,
  • Palma Scolieri,
  • Romina Andracco,
  • Francesco Girelli,
  • Elena Bravi,
  • Matteo Colina,
  • Alessandro Volpe,
  • Aurora Ianniello,
  • Maria Chiara Ditto,
  • Valeria Nucera,
  • Veronica Franchina,
  • Ilaria Platè,
  • Eleonora Di Donato,
  • Giorgio Amato,
  • Carlo Salvarani,
  • Simone Bernardi,
  • Gianluca Lucchini,
  • Francesco De Lucia,
  • Francesco Molica Colella,
  • Daniele Santilli,
  • Natalia Mansueto,
  • Giulio Ferrero,
  • Antonio Marchetta,
  • Eugenio Arrigoni,
  • Rosario Foti,
  • Gilda Sandri,
  • Vincenzo Bruzzese,
  • Marino Paroli,
  • Enrico Fusaro,
  • Alarico Ariani

DOI
https://doi.org/10.3390/biomedicines11020433
Journal volume & issue
Vol. 11, no. 2
p. 433

Abstract

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Background: To date, only a few real-world-setting studies evaluated apremilast effectiveness in psoriatic arthritis (PsA). The aims of this retrospective observational study are to report long-term Disease Activity Index for Psoriatic Arthritis (DAPSA) response of apremilast in PsA patients and to analyze the predictors of clinical response. Methods: All PsA consecutive patients treated with apremilast in fifteen Italian rheumatological referral centers were enrolled. Anamnestic data, treatment history, and PsA disease activity (DAPSA) at baseline, 6 months, and 12 months were recorded. The Mann–Whitney test and chi-squared tests assessed the differences between independent groups, whereas the Wilcoxon matched pairs signed-rank test assessed the differences between dependent samples. Logistic regressions verified if there were factors associated with achievement of DAPSA low disease activity or remission at 6 and 12 months. Results: DAPSA low disease activity or remission rates at 6 and 12 months were observed, respectively, in 42.7% (n = 125) and 54.9% (n = 161) patients. Baseline DAPSA was inversely associated with the odds of achieving low disease activity or remission at 6 months (odds ratio (OR) 0.841, 95% confidence interval (CI) 0.804–0.879; p p < 0.01). Conclusions: Almost half of the PsA patients receiving apremilast achieved DAPSA low disease activity or remission at 6 and 12 months. The only factor associated with achievement of low disease activity or remission at both 6 and 12 months was baseline DAPSA.

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