Gender-specific differences in patients with psoriatic arthritis receiving ustekinumab or tumour necrosis factor inhibitor: real-world data.

Autor: Kuijk, Arno W R Van, Nurmohamed, Mike T, Siebert, Stefan, Bergmans, Paul, Vlam, Kurt de, Gremese, Elisa, Joven-Ibáñez, Beatriz, Korotaeva, T V, Lavie, Frederic, Sharaf, Mohamed, Noël, Wim, Theander, Elke, Smolen, Josef S, Gossec, Laure, Horst-Bruinsma, Irene E van der
Předmět:
Zdroj: Rheumatology; Oct2023, Vol. 62 Issue 10, p3382-3390, 9p
Abstrakt: Objective Investigate effects of gender on disease characteristics and treatment impact in patients with PsA. Methods PsABio is a non-interventional European study in patients with PsA starting a biological DMARD [bDMARD; ustekinumab or TNF inhibitor (TNFi)]. This post-hoc analysis compared persistence, disease activity, patient-reported outcomes and safety between male and female patients at baseline and 6 and 12 months of treatment. Results At baseline, disease duration was 6.7 and 6.9 years for 512 females and 417 males respectively. Mean (95% CI) scores for females vs males were: clinical Disease Activity Index for Psoriatic Arthritis (cDAPSA), 32.3 (30.3, 34.2) vs 26.8 (24.8, 28.9); HAQ-Disability Index (HAQ-DI), 1.3 (1.2, 1.4) vs 0.93 (0.86, 0.99); total PsA Impact of Disease-12 (PsAID-12) score, 6.0 (5.8, 6.2) vs 5.1 (4.9, 5.3), respectively. Improvements in scores were smaller in female than male patients. At 12 months, 175/303 (57.8%) female and 212/264 (80.3%) male patients achieved cDAPSA low disease activity, 96/285 (33.7%) and 137/247 (55.5%), achieved minimal disease activity (MDA), respectively. HAQ-DI scores were 0.85 (0.77, 0.92) vs 0.50 (0.43, 0.56), PsAID-12 scores 3.5 (3.3, 3.8) vs 2.4 (2.2, 2.6), respectively. Treatment persistence was lower in females than males (P   ≤  0.001). Lack of effectiveness was the predominant reason to stop, irrespective of gender and bDMARD. Conclusions Before starting bDMARDs, females had more severe disease than males and a lower percentage reached favourable disease states, with lower persistence of treatment after 12 months. A better understanding of the mechanisms underlying these differences may improve therapeutic management in females with PsA. Trial registration ClinicalTrials.gov, https://clinicaltrials.gov , NCT02627768 [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index