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Author Spotlight: Self-Assessment Protocol for Predicting Psoriatic Arthritis in Psoriasis Patients
Published on: March 1, 2024
Understanding difficult-to-treat psoriatic arthritis: Data from the Rheumatic Diseases Portuguese Registry
Catarina Abreu1, Vanessa Fraga1, Sara Dias Rodrigues2
1Rheumatology Department, Hospital Garcia de Orta, Unidade Local de Saúde Almada-Seixal, Avenida Torrado da Silva, 2805-267 Almada, Portugal.
Difficult-to-treat psoriatic arthritis (D2T PsA) affects 0.9%-3.7% of patients. Predictors include polyarticular disease and higher baseline disease activity, indicating a need for early intervention in psoriatic arthritis management.
Area of Science:
- Rheumatology
- Immunology
- Clinical Medicine
Background:
- Psoriatic arthritis (PsA) is a chronic inflammatory condition.
- Identifying difficult-to-treat (D2T) PsA is crucial for optimizing patient outcomes.
- Current understanding of D2T PsA prevalence and predictors requires further investigation.
Purpose of the Study:
- To estimate the proportion of patients with difficult-to-treat psoriatic arthritis (D2T PsA).
- To identify clinical and demographic predictors associated with D2T PsA.
- To inform clinical practice and future research directions for managing challenging PsA cases.
Main Methods:
- A multicentre observational retrospective study utilizing data from the Rheumatic Diseases Portuguese Registry (Reuma.pt).
- Two distinct definitions were employed to classify D2T PsA based on treatment failure (≥2 or ≥3 b/tsDMARDs with different MoAs) and active/progressive disease signs.
- Statistical analysis was performed to identify associated predictors.
Main Results:
- The study included 1873 patients, with D2T PsA proportions of 3.7% and 0.9% based on the two definitions.
- D2T PsA was significantly associated with younger age at onset/diagnosis, polyarticular phenotype, depression, enthesitis, and lower BMI.
- Patients with D2T PsA exhibited higher baseline tender/swollen joint counts and DAPSA scores, along with increased rates of treatment discontinuation.
Conclusions:
- The prevalence of D2T PsA ranges from 0.9% to 3.7%.
- Key predictors of D2T PsA include polyarticular disease, higher baseline swollen joint count, and longer treatment duration on initial b/tsDMARDs.
- D2T PsA patients present with greater disease activity prior to first-line biologic/targeted synthetic DMARDs initiation and experience higher treatment discontinuation rates.
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