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: 1213

Transitional Changes on High Resolution Computed Tomography (HRCT) in idiopathic inflammatory Myopathy- Associated Interstitial Lung Disease (IIM-ILD)

Sangmee Bae1, Grace Kim2, Jihey Lee2, Daniela Markovic2, Donald Tashkin2, Jonathan Goldin2, Rohit Aggarwal3 and Christina Charles-Schoeman4, 1UCLA Rheumatology, Los Angeles, CA, 2UCLA, Los Angeles, 3University of Pittsburgh, Rheumatology and Clinical Immunology, Pittsburgh, United States of America, Pittsburgh, PA, 4UCLA Medical Center, Santa Monica, CA

Meeting: ACR Convergence 2025

Keywords: Imaging, interstitial lung disease, longitudinal studies, Myositis

  • 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: Monday, October 27, 2025

Title: (1191–1220) Muscle Biology, Myositis & Myopathies – Basic & Clinical Science Poster II

Session Type: Poster Session B

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

Background/Purpose: HRCT is used as a surrogate for important histopathological findings when evaluating patients with interstitial lung disease (ILD). Quantitative imaging analysis (QIA) using CT texture-based scores were shown to associate with lung physiology and patient reported outcomes in IIM-ILD. The current work aims to examine changes in HRCT patterns of IIM-ILD as they transition from one pattern to another during follow-up, and compare transition patterns of IIM-ILD to that of ILD related to systemic sclerosis (SSc-ILD).

Methods: We evaluated changes in the quantitative extent of ground glass, fibrotic pattern and normal lung obtained at baseline and follow-up in HRCT scans. Patients with ILD confirmed by HRCT and on immunosuppressive treatment were included from 2 longitudinal IIM-ILD cohorts. In each within-patient baseline to follow-up HRCT pair, we calculated the transitional probability expressed as a proportion of voxels representing a particular pattern of ILD that changes from the initial pattern to another pattern at follow-up, the denominator being the total number of voxels within the initial pattern at baseline. Net improvements in ground glass and fibrotic patterns were determined by subtracting unfavorable transitional probabilities from favorable ones and statistically analyzed with the null hypothesis of net improvement being 0. In order to compare transitional probability with SSc-ILD, we selected IIM-ILD patients with comparable follow up time between HRCTs to the Scleroderma Lung Study II (SLS II) for which transitional probability had previously been reported using similar methodology (PMID:31430058).

Results: Transitional probability was calculated in 70 IIM-ILD patients that had baseline and follow-up HRCT scans adequate for voxelwise registration. The cohort included 53% antisynthetase and 37% dermatomyositis associated ILD patients with a mean disease duration of 3.5 years (Table 1). Mean transitional probability for each transition pattern is shown in Figure 1. Fifty-five percent of baseline ground glass and 46% of baseline fibrosis transitioned to a normal pattern. Net probabilities of improvement for both ground glass to normal transition (PGG→NORML- PNORML→GG) and fibrosis to normal transition (PFibro→NORML – PNORML→Fibro) were significant (mean 0.44 and 0.39 respectively, p< 0.0001 for both). We compared transitional probabilities of 36 IIM-ILD patients with those in SLS II (Table 2). Favorable transitional probabilities (PGG→NORML, PFibro→NORML, PFibro→GG) were significantly greater in IIM-ILD compared to SSc-ILD patients whereas the majority of SSc-ILD remained stable. Unfavorable transitional probabilities (PNORML→GG, PGG→Fibro and PNORML→Fibro) were overall low in both groups, showing a slight trend to be greater in the IIM-ILD compared to the SSc-ILD group (2/3 comparisons not statistically significant).

Conclusion: Transitional scoring assessment of ILD demonstrated that significant portions of ground glass and fibrotic patterns at baseline transitioned to a normal pattern with treatment in both IIM and SSc patients with ILD. However, IIM-ILD had significantly greater proportions of favorable transition patterns than SSc-ILD.

Supporting image 1Values are presented as mean±SD

IIM-ILD group(n=70) is comprised of 2 separate cohorts: one single-center observational cohort (n=59) and one multicenter clinical trial cohort of antisynthetase ILD (Attack My-ILD ClinicalTrials.gov identifier: NCT03215927, n=11)

¶ Data unavailable at time of abstract submission

Abbreviations: IIM, idiopathic inflammatory myopathy; IMNM, immune mediated necrotizing myopathy; VAS, visual analog scale; PFT, pulmonary function test; QIA, quantitative imaging analysis; QGG, quantitative ground glass score; QLF, quantitative lung fibrosis score; QILD, quantitative total ILD score; MAA, myositis associated antibody (Ro, Ku, Pm-scl)

Supporting image 2

Supporting image 3


Disclosures: S. Bae: None; G. Kim: UCLA for patent; consultant at Voiant, 2, 10; J. Lee: None; D. Markovic: None; D. Tashkin: None; J. Goldin: MEDQIA, 12, Founder; R. Aggarwal: Alexion, 2, ANI Pharmaceuticals, 2, Argenx, 2, Artasome, 2, AstraZeneca, 2, Boehringer-Ingelheim, 2, 5, Bristol-Myers Squibb(BMS), 2, 5, CabalettaBio, 2, Capella, 2, Capstanx, 2, CSL Behring, 2, EMD Serono, 2, 5, Galapagos, 2, Horizon Therapeutics, 2, I-Cell, 2, Immunovant, 2, Janssen, 2, 5, Kezar, 2, Kyverna, 2, Lilly, 2, Manta Medicines, 2, Nkarta, 2, Novartis, 2, Octapharma, 2, Pfizer, 2, 5, Priovant, 2, 5, Teva, 2, Tourmaline Bio, 2, UCB, 2, Verismo Therapeutics, 2; C. Charles-Schoeman: AbbVie/Abbott, 2, 5, Alexion, 5, Boehringer-Ingelheim, 2, Bristol-Myers Squibb(BMS), 2, 5, CSL Behring, 5, Galapagos, 2, Immunovant, 2, Janssen, 5, Octapharma, 2, 5, Pfizer, 2, 5, Priovant, 5, Recludix, 2, Sana Biotechnology, 2.

To cite this abstract in AMA style:

Bae S, Kim G, Lee J, Markovic D, Tashkin D, Goldin J, Aggarwal R, Charles-Schoeman C. Transitional Changes on High Resolution Computed Tomography (HRCT) in idiopathic inflammatory Myopathy- Associated Interstitial Lung Disease (IIM-ILD) [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/transitional-changes-on-high-resolution-computed-tomography-hrct-in-idiopathic-inflammatory-myopathy-associated-interstitial-lung-disease-iim-ild/. 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/transitional-changes-on-high-resolution-computed-tomography-hrct-in-idiopathic-inflammatory-myopathy-associated-interstitial-lung-disease-iim-ild/

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