RMD Open (Nov 2023)

Early axial spondyloarthritis according to the ASAS consensus definition: characterisation of patients and effectiveness of a first TNF inhibitor in a large observational registry

  • Oliver Distler,
  • Diego Kyburz,
  • Adrian Ciurea,
  • Michael J Nissen,
  • Andrea Rubbert-Roth,
  • Raphael Micheroli,
  • Almut Scherer,
  • Kristina Bürki,
  • Pascale Exer,
  • Burkhard Möller,
  • Michael Andor,
  • René Bräm,
  • Thomas Hügle,
  • Andrea Götschi

DOI
https://doi.org/10.1136/rmdopen-2023-003455
Journal volume & issue
Vol. 9, no. 4

Abstract

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Objective To characterise the population fulfilling the Assessment of SpondyloArthritis international Society (ASAS) consensus definition of early axial spondyloarthritis (axSpA) and to determine the effectiveness of a first tumour necrosis factor inhibitor (TNFi) in early versus established axSpA in a large observational registry.Methods A total of 3064 patients with axSpA in the Swiss Clinical Quality Management registry with data on duration of axial symptoms were included (≤2 years=early axSpA, N=658; >2 years=established axSpA, N=2406). Drug retention was analysed in patients starting a first TNFi in early axSpA (N=250) versus established axSpA (N=874) with multiple-adjusted Cox proportional hazards models. Adjusted logistic regression analyses were used to determine the achievement of the ASAS criteria for 40% improvement (ASAS40) at 1 year.Results Sex distribution, disease activity, impairments of function and health-related quality of life were comparable between patients with early and established axSpA. Patients with established disease were older, had more prevalent axial radiographical damage and had a higher impairment of mobility. A comparable TNFi retention was found in early versus established disease after adjustment for age, sex, human leucocyte antigen-B27 status, education, body mass index, smoking, elevated C reactive protein and sacroiliac inflammation on MRI (HR 1.05, 95% CI 0.78 to 1.42). The adjusted ASAS40 response was similar in the two groups (OR 1.09, 95% CI 0.67 to 1.78). Results were confirmed in the population fulfilling the ASAS classification criteria.Conclusion Considering the recent ASAS definition of early axSpA, TNFi effectiveness seems comparable in early versus established disease.