ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2333

Validation of a Corrected Axial Spondyoarthritis Metrology Index in 9 Randomized Clinical Trials

Dafne capelusnik1, Philip Gardiner2, Annelies Boonen3, Elena Nikiphorou4 and Sofia Ramiro5, 1Tel Aviv Sourasky Medical Center, Ramat Gan, Israel, 2Altnagelvin Hospital, Londonderry, United Kingdom, 3Maastricht University Medical Centre+ & Maastricht University, Maastricht, Limburg, Netherlands, 4King’s College London, London, United Kingdom, 5Leiden University Medical Center, Bunde, Netherlands

Meeting: ACR Convergence 2025

Keywords: Ankylosing spondylitis (AS), clinical trial, Outcome measures, spondyloarthritis, Statistical methods

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, October 28, 2025

Title: (2305–2337) Spondyloarthritis Including Psoriatic Arthritis – Diagnosis, Manifestations, & Outcomes Poster III

Session Type: Poster Session C

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

Background/Purpose: The MOBILITY study showed that BASMI often misclassifies spinal mobility, especially in older and taller individuals. To address this, the Corrected AxSpA Metrology Index (CASMI) was developed by adjusting BASMI for age, height, and sex to remove the variability introduced by these factors. This study evaluates CASMI’s psychometric properties and compares them with BASMI in RCTs of axSpA patients treated with b/tsDMARDs.

Methods: RCTs in axSpA patients with complete BASMI component data (lateral spinal flexion, tragus-to-wall distance, intermalleolar distance, cervical rotation, and lumbar flexion) at baseline and the timing of the primary endpoint were included. Data were accessed and analyzed via the data-sharing platform Vivli. Age, sex, and height were used to adjust individual spinal mobility measures. BASMI- and CASMI-linear were calculated, and the following psychometric properties were analyzed: Construct validity: Known-group discrimination (Standardized Mean Difference -SMD) at baseline to distinguish between low and high functional impairment (BASFI < 3 vs >6); Longitudinal construct validity: Standardized Response Mean (SRM), Guyatt’s responsiveness index (GRI), and effect size (ES); Trial discrimination: SMD. For all these psychometric properties, performance was classified as follows: low performance: < 0.5; adequate performance: ≥0.5 and < 0.8; good performance: ≥0.8. Lastly, a sensitivity analysis was conducted in patients with early disease (≤2 years of symptom duration).

Results: Nine RCTs, all having reached the primary endpoint, with complete BASMI component data and available age, sex, and height information were included. Six involved radiographic axSpA, three non-radiographic axSpA. Only 5 studies included patients with early disease and in varying proportions: 3–48%. In seven of nine trials, CASMI had a lower mean value than BASMI (Table). For construct validity, most trials showed good discriminatory capacity, except COAST-W (TNFi-insuficient response population) and SELECT-AXIS. EMBARK was the only trial where CASMI showed a good discrimination between know-groups, while for BASMI it was only adequate. Regarding longitudinal construct validity, results were inconclusive, showing high variability across measures, but without important differences between BASMI and CASMI. All trials in bDMARD-naïve r-axSpA patients showed significant BASMI/CASMI improvements with active treatment, but trial discrimination was generally low for both, except for CASMI in ASSERT (adequate) and TOFACITINIB (good). In all nr-axSpA studies, trial discrimination was low for both BASMI and CASMI. In analyses restricted to early disease patients, trial discrimination improved numerically but remained low (except for TOFACITINIB, where it remained good), with the exception of SELECT-AXIS, where discrimination became good for BASMI and adequate for CASMI.

Conclusion: While CASMI has been developed to be a more truthful measure than BASMI, both CASMI and BASMI have largely comparable measurement properties. This means that the current adjustments are still insufficient to detect change over time in spinal mobility.

Supporting image 1


Disclosures: D. capelusnik: None; P. Gardiner: AbbVie/Abbott, 1, Galapagos, 1, Gilead, 1, Pfizer, 1, UCB, 1; A. Boonen: AbbVie/Abbott, 5, Alfasigma, 2, Celgene, 5, Eli Lilly, 2, Novartis, 2, Sandoz, 2, UCB, 2; E. Nikiphorou: AbbVie/Abbott, 1, Alfasigma, 1, Eli Lilly, 1, 5, Fresenius, 1, Galapagos, 1, Gilead, 1, Novartis, 1, Pfizer, 1, 5, UCB, 1; S. Ramiro: AbbVie, 2, 5, Eli Lilly, 2, 5, Galapagos/Alfasigma, 2, 5, Janssen, 2, MSD, 2, 5, Novartis, 2, 5, Pfizer, 2, 5, Sanofi, 2, 5, UCB, 2, 5.

To cite this abstract in AMA style:

capelusnik D, Gardiner P, Boonen A, Nikiphorou E, Ramiro S. Validation of a Corrected Axial Spondyoarthritis Metrology Index in 9 Randomized Clinical Trials [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/validation-of-a-corrected-axial-spondyoarthritis-metrology-index-in-9-randomized-clinical-trials/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2025

ACR Meeting Abstracts - https://acrabstracts.org/abstract/validation-of-a-corrected-axial-spondyoarthritis-metrology-index-in-9-randomized-clinical-trials/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

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.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology