August 11, 2026 – A study initiated by the European Spondyloarthritis Research Collaboration Network (EuroSpA) examined whether where patients with psoriatic arthritis (PsA) or axial spondyloarthritis (axSpA) live is associated with the severity of their disease, when they begin advanced treatment, and how long they continue that treatment. Findings in the Annals of the Rheumatic Diseases ( ARD ), The EULAR Journal, published by Elsevier, found evidence that patients from wealthier European countries tend to start treatment with biologics earlier but also stop or switch treatment earlier. They also experience lower disease activity at treatment start than patients in middle- and low-income countries.
“We observed that patients’ disease activity and treatment outcomes varied across countries and wanted to understand whether differences in socioeconomic conditions between countries could explain some of these variations,” explains lead investigator Brigitte Michelsen, MD, PhD, Copenhagen Center for Arthritis Research (COPECARE), Rigshospitalet, Glostrup, Denmark; Sørlandet Hospital, Kristiansand, Norway; and Diakonhjemmet Hospital, Oslo, Norway.
Importantly, this research moves beyond individual patient factors and examines country-level socioeconomic influences on treatment outcomes across a large, real-world European cohort of patients. The study included 38,911 patients (17,296 with PsA and 21,615 with axSpA) in 13 European countries who began treatment with biologic or targeted synthetic disease-modifying anti-rheumatic drugs (b/tsDMARDs) between 2015 and 2021. It assessed treatment retention at 6, 12, and 24 months after patients started treatment. Countries were categorized as low-, medium-, and high-income, according to national socioeconomic indicators.
Key Findings:
This research highlights that national healthcare context and identifying system level inequalities matter. The cross-country differences identified should be recognized when interpreting treatment retention and outcomes. Further, the findings emphasize the importance of ensuring timely and equitable access to effective treatment for patients with PsA and axSpA, while also using advanced therapies appropriately and equitably.
The study highlights that countries with lower resources may need to focus on earlier identification of insufficient disease control and improved access to effective therapies, while high-income countries may need to ensure that frequent switching is clinically justified and aligned with patient benefit.
“This research is particularly important at this time because, although advanced treatment options have improved treatment practices, health system resources continue to differ between countries. For clinicians and policymakers, our findings highlight the importance of ensuring timely and equitable access to effective treatment for patients with PsA and axSpA, while also using these advanced therapies appropriately and equitably. This is of utmost relevance now, as health systems are increasingly focused on equitable access, cost-effective use of expensive therapies, and reducing unwarranted variation in care across countries,” concludes Dr. Michelsen.
“This is another important piece of evidence of how healthcare systems influence the approach to managing patients with various rheumatic diseases,” adds ARD Editor-in-Chief Josef Smolen, MD, from the Medical University of Vienna. “At ARD one of our primary roles is to improve equity in patient care across the globe, and the study by Michelsen and co-investigators constitutes an important example to further our understanding of inequities and improve care of patients with musculoskeletal and rheumatic diseases in the world.”
Annals of the Rheumatic Diseases
Data/statistical analysis
People
Influence of national socioeconomic status on treatment retention and disease activity in psoriatic arthritis and axial spondyloarthritis: evidence over 2 years in 13 European countries
13-Jul-2026
This EuroSpA study was financially supported by Novartis. No financial sponsors had any influence on the data collection, statistical analyses, manuscript preparation, or decision to submit.