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Abstract Number: 0428

The OMERACT Juvenile Idiopathic Arthritis MRI Score for Active and Structural Lesions in the Sacroiliac Joints: Development and Validation in Two Longitudinal Cohorts

Walter P. Maksymowych1, Michael Francavilla2, Nele Herregods3, Robert G. W. Lambert4, Arthur Meyers5, Joel Paschke6, Jennifer Stimec7, Pamela Weiss8 and Dax Rumsey9, 1Department of Medicine, University of Alberta, 568 Heritage Building, Edmonton, AB, Canada, 2Department of Pediatric Radiology, Children’s Hospital Philadelphia, Philadelphia, PA, 3Department of Pediatric Radiology, Ghent University Hospital, Ghent, Belgium, 4University of Alberta, Department of Radiology & Diagnostic Imaging, Edmonton, AB, Canada, 5Department of Radiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 6CARE Arthritis Limited, Edmonton, AB, Canada, 7Department of Diagnostic Imaging, SickKids, University of Toronto, Toronto, Canada, 8Childrens Hospital of Philadelphia, Philadelphia, PA, 9Department of Pediatrics, University of Alberta, Edmonton, AB, Canada

Meeting: ACR Convergence 2025

Keywords: Imaging, Magnetic resonance imaging (MRI), Pediatric rheumatology, spondyloarthritis

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Session Information

Date: Sunday, October 26, 2025

Title: (0387–0429) Pediatric Rheumatology – Clinical Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: The OMERACT Juvenile Idiopathic Arthritis MRI (JAMRIS) Working group has defined a spectrum of MRI lesions in the sacroiliac joint (SIJ) in youth with spondyloarthritis and axial disease (axJSpA) that can be included in a scoring method. Previous reports have described the application of Spondyloarthritis Research Consortium of Canada (SPARCC) methodology to quantify MRI SIJ lesions in axJSpA, where assessment of inflammation is limited to bone marrow edema (BME) and lesions are assessed in a limited number of semicoronal slices. We aimed to assess the impact of including all inflammatory lesions and SPARCC methodology versus an all-slice method on the metrology of JAMRIS in two longitudinal cohorts of youth with axJSpA treated with a tumor necrosis factor inhibitor (TNFi).

Methods: The two cohorts recruited youth with axJSpA who had a rheumatologist diagnosis of axJSpA. All subjects underwent MRI as part of a diagnostic evaluation for axial disease. MRI lesions were assessed on semicoronal slices through the SIJ from the most anterior (≥1cm vertical height of cartilaginous portion) to the most posterior (≥1cm visible cartilaginous portion) slice. Structural lesions were assessed first on the T1-weighted scan followed by inflammatory lesions on a fluid-sensitive sequence. Scans were obtained at baseline and 3 months-1 year follow up after initiation of treatment with TNFi and assessed blinded-to timepoint and clinical details by 7 readers (4 pediatric and 1 adult MSK radiologists, 1 adult and 1 pediatric rheumatologist) after standardized calibration using a CARE Arthritis online module. MRI lesions were recorded based on standardized lesion definitions derived from ASAS and the JAMRIS group in a standardized eCRF (ASAS MRImagine). Analyses included descriptive statistics, reliability (intraclass correlation coefficient (ICC), smallest detectable difference (SDD) or change (SDC)), and responsiveness (standardized response mean (SRM)).

Results: Pre- and post-treatment scans (mean(SD) duration between scans 46.6(47.1) weeks) were available from 60 cases, 30 from each cohort. An inflammatory lesion in addition to BME was recorded in 41(68.3%) cases by a majority of readers. But only 1 case had an inflammatory lesion without any BME. For change in structural lesion scores after TNFi treatment, minimal differences were evident between SPARCC and all slice methodologies (Figure 1A). The major contributor to change in inflammatory lesion scores was BME followed by inflammation in an erosion cavity (IEC), though differences between SPARCC and all slice methodologies were minimal (Figure 1B). Reliability for detection of change scores was comparable between SPARCC and all slice methodologies (Table). Responsiveness was comparable between methodologies and combining scores for inflammatory lesions was not superior to BME alone (Figure 2).

Conclusion: BME is the most responsive lesion to treatment with TNFi in axJSpA followed by IEC and then erosion. Responsiveness is not enhanced by assessment of all slices as compared to SPARCC nor by scoring additional inflammatory lesions beyond BME.

Supporting image 1Figure 1. Change from baseline values (in boxes) in A. MRI structural lesion scores (SIJ quadrants for erosion, sclerosis, and fat lesion, SIJ halves for backfill and ankylosis) and B. MRI inflammation scores (SIJ quadrants for BME and inflammation in an erosion cavity (IEC)), after TNFi assessed across all SIJ slices or limited to the slices selected in the SPARCC methods.

Supporting image 2Table. Reliability of change scores for MRI SIJ inflammatory and structural lesions for all 7 readers, MSK radiologists (n=5), and rheumatologists (n=2). SDC smallest detectable change.

Supporting image 3Figure 2. Standardized response means for MRI SIJ inflammatory and structural lesions scores after TNFi assessed across all SIJ slices or limited to the slices selected in the SPARCC method. IEC inflammation in an erosion cavity


Disclosures: W. Maksymowych: AbbVie, 2, 5, 6, BMS, 2, 5, 6, Boehringer-Ingelheim, 2, Celgene, 2, Chief Medical Officer for CARE ARTHRITIS, 4, Eli Lilly, 2, 5, 6, Galapagos, 2, 5, 6, Janssen, 2, 6, Novartis, 2, 5, 6, Pfizer, 2, 5, 6, UCB, 2, 5, 6; M. Francavilla: None; N. Herregods: None; R. Lambert: AbbVie, 2, CARE Arthritis and Image Analysis Group, 2; A. Meyers: Elsevier, 9, Pfizer, 2; J. Paschke: CARE Arthritis Limited, 3; J. Stimec: None; P. Weiss: Bristol-Myers Squibb(BMS), 2, Pfizer, 1; D. Rumsey: None.

To cite this abstract in AMA style:

Maksymowych W, Francavilla M, Herregods N, Lambert R, Meyers A, Paschke J, Stimec J, Weiss P, Rumsey D. The OMERACT Juvenile Idiopathic Arthritis MRI Score for Active and Structural Lesions in the Sacroiliac Joints: Development and Validation in Two Longitudinal Cohorts [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/the-omeract-juvenile-idiopathic-arthritis-mri-score-for-active-and-structural-lesions-in-the-sacroiliac-joints-development-and-validation-in-two-longitudinal-cohorts/. Accessed .
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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