AI Article Synopsis

  • Uveitis is a common complication in patients with Spondyloarthritis (SpA), and this study examined how frequently it occurs, its geographical variations, and whether it has changed since the introduction of biologic treatments.
  • A total of 3984 patients across 22 countries were assessed, revealing that the likelihood of experiencing uveitis increases significantly over time, with various factors like HLA-B27 positivity and a family history of uveitis linked to a higher risk.
  • Results indicated a drastic reduction in the prevalence and incidence of uveitis in patients who started treatment after 2000, suggesting that biologic therapies may help mitigate this condition.

Article Abstract

Objectives: Uveitis is a common extra-musculoskeletal manifestation in Spondyloarthritis (SpA). The aim of this study was to analyze the prevalence of uveitis in SpA patients, its association with geographical areas and to determine whether its incidence was different before and after the biological era.

Methods: ASAS-COMOSPA is a retrospective study that includes patients fulfilling ASAS SpA classification criteria from 22 countries. The overall prevalence of uveitis was calculated, and factors associated with the onset of a first episode of uveitis were evaluated using a Cox regression. A Log-Rank test was performed to compare the new onset of uveitis in the no biological era (SpA onset before 2000) vs biological era (SpA onset after 2000).

Results: 3984 patients were included. The likelihood of presenting a first uveitis episode increased over time, from a prevalence of 10.5% (95%CI 9.5%-11.4%) at the time of the SpA diagnosis to 46.6% (41.6%-51.5%) after 30 years since the SpA diagnosis. HLA-B27 positivity, family history of uveitis, peripheral enthesitis and IBD were associated with higher risk of uveitis. Patients with SpA disease onset after year 2000 showed a lower prevalence of uveitis compared with disease onset before year 2000 (8.2% vs 25.5%, p< 0.01), as well as a lower incidence (2.8 per 100 PY vs 6.1 per 100 PY, respectively).

Conclusion: In our study the risk of having suffered from at least one episode of uveitis ranged from 10% at the time of the diagnosis of axSpA to 47% after 30 years of disease duration. Patients with disease onset after biologic therapy introduction showed a significantly lower prevalence and incidence of first episodes of uveitis.

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Source
http://dx.doi.org/10.1093/rheumatology/keae536DOI Listing

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