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Prevalence and clinical factors associated with difficult-to-manage axial spondyloarthritis: a multicentre Italian cohort study with meta-analysis

Journal
Therapeutic advances in musculoskeletal disease (Q1)
Published
30 August 2026
Study design
Systematic review of cohort studies
Evidence level
Level 2, Moderate (CEBM 2a)
Authors
Giulio Forte, Gilberto Cincinelli, Daniele Mauro, Ilenia Pantano, Matteo Ferrito, Saviana Gandolfo, et al.
PMID
42676533
DOI
10.1177/1759720X261434275

Why clinicians should know about it

  • Picked for Rheumatology (paper of the day, 7 September 2026): Difficult‑to‑manage axial spondyloarthritis prevalence study

Abstract

BACKGROUND: The concept of difficult-to-manage axial spondyloarthritis (D2M-axSpA) has recently been introduced to describe patients with a persistent disease burden despite appropriate treatment. However, its real-world prevalence and associated clinical features remain insufficiently characterised. OBJECTIVE: To estimate the prevalence of D2M and treatment-refractory (TR) axSpA in routine clinical practice, identify factors associated with D2M, and assess the consistency of selected D2M-associated features across different cohorts. DESIGN AND METHODS: A cross-sectional study was conducted in 252 patients with axSpA from two Italian tertiary centres. The 2024 Assessment of Spondyloarthritis International Society consensus-based definition was applied to identify D2M and TR axSpA. Clinical, laboratory and imaging characteristics were compared between D2M and non-D2M patients. Factors independently associated with D2M were evaluated using multivariable logistic regression. To explore consistency across populations, an exploratory meta-analysis was performed using harmonised data from the published Argentinian Reuma-Check cohort. RESULTS: Among 252 patients with axSpA, 16 (6.3%) fulfilled the definition of D2M, and 8 (3.2%) met criteria for TR axSpA. Patients with D2M exhibited higher disease activity (Axial Spondyloarthritis Disease Activity Score 2.50 ± 0.62 vs 1.24 ± 0.65; p < 0.001), greater axial pain (2.50 ± 2.75 vs 0.80 ± 1.63; p = 0.017) and worse global assessments (Patient Global Assessment 3.20 vs 1.16; p < 0.001). In multivariable analysis, fibromyalgia (odds ratios (OR) 5.5, 95% confidence interval (CI): 1.2-25.6) and a history of uveitis (OR 3.3, 95% CI: 1.0-11.1) were independently associated with D2M status. Current nonsteroidal anti-inflammatory drug (NSAID) use (OR 3.8, 95% CI: 1.2-11.9) was also associated with D2M, most likely reflecting higher symptom burden rather than a causal relationship. Meta-analytic findings identified psoriasis (risk ratios (RR) 2.17; p = 0.008), smoking (RR 1.53; p = 0.045), uveitis (RR 2.45; p = 0.044) and radiographic structural damage (RR 1.84; p = 0.004) as consistent features associated with D2M axSpA. CONCLUSION: D2M axSpA was identified in approximately 6.3% of patients, while 3.2% fulfilled criteria for TR axSpA. Fibromyalgia, NSAID use and uveitis were independently associated with the D2M phenotype, whereas meta-analytic evidence highlighted additional associations with psoriasis, smoking and structural damage. These findings support the multifactorial nature of D2M axSpA, in which both inflammatory and non-inflammatory mechanisms contribute to disease complexity.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.