Latest Developments in Imaging for Axial Disease in Psoriatic Arthritis

Authors

  • Walter P. Maksymowych, MB, ChB, MRCP (UK), FACP, FRCPC Professor of Medicine, University of Alberta, Edmonton, Alberta, Canada; Chief Medical Officer, CARE Arthritis Limited, Edmonton, Canada.

DOI:

https://doi.org/10.58931/crt.2025.2367

Abstract

Axial disease in psoriatic arthritis (axPsA), affecting the sacroiliac joints (SIJ) and spine, is recognized as one of the domains in the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) treatment recommendations for psoriatic arthritis (PsA). Accurate recognition of this manifestation is crucial for comprehensive management of this disease. It is defined according to both clinical and imaging features. Clinically, inflammatory back pain (IBP) is a key feature; however, findings from a recent Canadian inception cohort study—Screening for Axial Spondyloarthritis in Psoriasis, Iritis, or Colitis Cohorts 1 and 2 (SASPIC1 and 2)—which included patients with psoriasis and undiagnosed back pain, showed no differences in the frequency of IBP or non-steroidal anti-inflammatory drug (NSAID) responsiveness between those diagnosed with axPsA and individuals with other causes of chronic back pain. Similarly, data from the global Axial Involvement in Psoriatic Arthritis (AXIS) cohort revealed only minor numerical differences in NSAID responsiveness or frequency of IBP, according to the ASAS criteria, between participants with and without axial involvement when evaluated by central reviewers. Recent post-hoc studies of clinical trials in PsA have attempted to identify axPsA according to a Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) threshold of ≥4. However, MRI-based assessment of axPsA in a large European cohort of 581 PsA patients, recruited across 17 European registries within the EuroSpA network, indicated that a BASDAI ≥4 did not discriminate PsA patients with axial disease from those without. Moreover, only 25–45% of patients with radiographic features of axPsA have been reported to have IBP, with some patients being clinically perceived as asymptomatic. Additionally, axSpA-based IBP criteria have demonstrated limited specificity for axPsA. Studies using MRI have reported poor correlation between sacroiliitis on imaging and both the presence and type of back pain.

Author Biography

Walter P. Maksymowych, MB, ChB, MRCP (UK), FACP, FRCPC, Professor of Medicine, University of Alberta, Edmonton, Alberta, Canada; Chief Medical Officer, CARE Arthritis Limited, Edmonton, Canada.

Walter P. Maksymowych is a Professor, Clinician, and Medical Scientist in the Department of Medicine, Division of Rheumatology at the University of Alberta, Edmonton, Canada. He is Canadian Royal College and American Board of Internal Medicine certified in Internal Medicine and Rheumatology. He is the 2012 recipient of the Distinguished Investigator Award from the Canadian Rheumatology Association. He founded CARE Arthritis Limited, a Canadian company focused on the development of personalized medicine strategies for patients with arthritis, and now serves as Chief Medical Officer. Dr. Maksymowych graduated from the University of Manchester School of Medicine, United Kingdom, in 1981 and completed his postgraduate training at the Universities of Alberta, Canada, and Cincinnati, USA. His primary research interests are the imaging and treatment of spondyloarthritis, and the clinical validation of biomarker technologies for rheumatic diseases. He has published over 400 research articles and is an active member of numerous international societies related to arthritis. He is co-developer of the SPARCC MRI scoring systems for inflammation and structural damage in the sacroiliac joints and spine that are now industry standard in clinical trials. Most recently, he co‑invented the 14-3-3 biomarker which is now licensed for diagnostic testing of patients with rheumatoid arthritis.

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Published

2025-12-19

How to Cite

1.
Maksymowych WP. Latest Developments in Imaging for Axial Disease in Psoriatic Arthritis. Can Rheumatol Today [Internet]. 2025 Dec. 19 [cited 2025 Dec. 23];2(3):15–21. Available from: https://canadianrheumatologytoday.com/article/view/2-3-Maksymowych

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