Abstract
Purpose of Review
To review current understanding of the prevalence, clinical features, outcome measures and recent therapeutic trials in axial psoriatic arthritis (axPsA).
Recent Findings
The prevalence of axPsA is estimated at 40–50%. However, the definition of axPsA remains unclear, therefore these estimates may be inaccurate. Ax PsA appears to be distinct from ankylosing spondylitis in demographic, clinical, genetic and therapeutic features. Because of the lack of widely accepted definition of axPsA it has been difficult to design therapeutic trials for this domain of PsA.
Summary
Several studies have demonstrated the uniquness of axPsA. Few recent trials suggest that therapies that work for peripheral arthritis also work for axPsA.
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References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
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• Helliwell PS, Gladman DD, Chakravarty SD, et al. Effects of ustekinumab on spondylitis-associated endpoints in TNFi-naive active psoriatic arthritis patients with physician-reported spondylitis: pooled results from two phase 3, randomised, controlled trials. RMD Open. 2020;6(1):e001149 This analysis of patients including in the PSUMMIT 1 and 2 studies investigating the effect of ustekinumab in PsA demonstrated improvement in spinal endpoint in the subgroup of patients who had axial disease defined by a physician. The study is relevant since it suggests that IL-12/23 inhibition may work in axial PsA although it did not work in AS.
• Helliwell PS, Gladman DD, Poddubnyy D, et al. Efficacy of guselkumab, a monoclonal antibody that specifically binds to the p19-subunit of IL-23, on endpoints related to axial involvement in patients with active PsA with imaging-confirmed sacroiliitis: week-24 results from two phase 3, randomized, double-blind, placebo-controlled studies. Ann Rheum Dis. 2020;79(supplement 1):36 (Submitted for publication). This analysis of patients including in the DISCOVER 1 and 2 studies investigating the effect of guselkumab in PsA demonstrated improvement in spinal endpoint in the subgroup of patients who had axial disease confirmed by imaging. The study is relevant since it suggests that IL-23 p19 inhibition may work in axial PsA although it did not work in AS.
•• Baraliakos X, Gossec L, Poumara E, et al. Secukinumab improves clinical and imaging outcomes in patients with psoriatic arthritis and axial manifestations with inadequate response to NSAIDs: week 52 results from the MAXIMISE trial. Ann Rheum Dis. 2020;79(supplement 1):36 (Submitted for publication). This is the first study designed specifically to assess axial disease in PsA. Although the patient selection was based on physician definition of axial disease, at least half the patients had inflammatory changes on MRI. Both clinical and imaging responses were noted with secukinumab.
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Funding
Dr. Gladman’s research is supported by the Krembil Foundation, the Canadian Institutes of Health Research, and the National Psoriasis Foundation.
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This article does not contain any studies with human or animal subjects performed by any of the authors.
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Dr. Gladman has received trial grants and or consulting fees from AbbVie, Amgen, BMS, Eli Lilly, Galapagos, Gilead, Janssen, Novartis, Pfizer, and UCB.
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Key Points
• Ankylosing spondylitis and axial psoriatic arthritis are both part of the spectrum of spondyloarthritis and have overlapping features but also differ in their genetic, clinical, radiographic, and prognostic characteristics.
• HLA-B*27 occurs less frequently in axial psoriatic arthritis than in ankylosing spondylitis but is a genetic risk factor for both diseases.
• Axial psoriatic arthritis develops at an older age, is less symptomatic, and is associated with distinct radiographic features compared with ankylosing spondylitis.
• The majority of comparative studies to date have had a cross-sectional design, which captures patients at different stages of disease and hampers the true comparison of these two diseases.
• The lack of a universally accepted definition of axial psoriatic arthritis needs to be addressed.
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Gladman, D.D. Axial Psoriatic Arthritis. Curr Rheumatol Rep 23, 35 (2021). https://doi.org/10.1007/s11926-021-00999-8
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DOI: https://doi.org/10.1007/s11926-021-00999-8