All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional.
The PsOPsA Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the PsOPsA Hub cannot guarantee the accuracy of translated content. The PsOPsA Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The PsOPsA Hub is an independent medical education platform. This activity is supported by an educational grant from Lilly. Funders are allowed no direct influence on our content.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account to access:
Bookmark & personalize site content
Receive alerts for new content in your areas of interest
View psoriasis and psoriatic arthritis content recommended for you
Results from a propensity score-matched study, evaluating tirzepatide + biologic or targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs; n = 31) vs b/tsDMARDs alone (n = 62) in patients with psoriatic arthritis (PsA) and obesity or overweight with ≥1 weight-related comorbidity, were published in RMD Open by Venerito et al. Outcomes at 6 months included minimal disease activity (MDA; ≥5/7 criteria), Disease Activity Index for Psoriatic Arthritis (DAPSA) low disease activity (LDA) ≤14, PsA Impact of Disease-12 (PsAID-12), Patient Acceptable Symptom State (PASS) ≤4, Health Assessment Questionnaire (HAQ) ≤0.5, Psoriasis Area and Severity Index (PASI) ≤1, Visual Analog Scale (VAS) pain, and C-reactive protein (CRP).
Key data: At 6 months, the tirzepatide + b/tsDMARD group had greater reductions in body mass index (BMI; −2.9 kg/m² vs +0.4 kg/m²; p < 0.001) and CRP (4.2 mg/L vs 7.7 mg/L; p < 0.001); higher rates of PsAID-12 PASS (48% vs 21%; p = 0.009), HAQ ≤0.5 (42% vs 18%; p = 0.022), and PASI ≤1 (74% vs 52%; p = 0.045); and lower rates of VAS pain (33.1 vs 46.4; p = 0.028) compared with the b/tsDMARDs-alone group. While physician-assessed targets, including MDA (26% vs 16%; p = 0.279) and DAPSA LDA (84% vs 82%; p > 0.99), did not differ between groups, adjusting the 6-month value for the baseline showed reductions in DAPSA with tirzepatide + b/tsDMARD vs b/tsDMARD alone (−1.78; p = 0.016). Gastrointestinal (GI) adverse events (AEs), including nausea (35%) and diarrhea (19%), were common but manageable in patients receiving tirzepatide.
Key learning: Tirzepatide + b/tsDMARDs was associated with significant improvements in weight management, patient-reported outcomes (PROs), skin disease control, and baseline-adjusted joint disease activity, as well as reductions in CRP compared with b/tsDMARDs alone. Treating obesity and PsA concomitantly may represent a potential paradigm shift in the management of patients with PsA and obesity/overweight; however, further evaluation in larger randomized studies is needed.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content