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ABS0950 (2025)
ARTIFICIAL INTELLIGENCE ANALYSIS OF HRCT IMAGES REFLECTS PULMONARY INVOLVEMENT IN SYSTEMIC SCLEROSIS INTERSTITIAL LUNG DISEASE
Keywords: Lungs, Imaging, Artificial Intelligence
L. Thornton1,2, E. De Lorenzis1,3, S. Di Donato1, M. Minerba1, L. A. Bissell1, P. George4, F. Del Galdo1
1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom
2NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom
3Division of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico, University A.Gemelli IRCCS, Rome, Italy
4Royal Brompton Hospital London, Department of Interstitial Lung Disease, London, United Kingdom

Background: Interstitial lung disease (ILD) is the leading cause of mortality and morbidity in systemic sclerosis (SSc) patients. Current functional, imaging, and clinical measures of lung involvement could be biased in SSc due to its multiorgan nature, with extra-articular involvement (e.g., cardiac, musculoskeletal, oesophageal) potentially affecting pulmonary function tests, high-resolution computed tomography (HRCT) findings, and respiratory symptoms. Artificial intelligence (AI) reading of HRCT has emerged as a novel tool for the objective and reliable assessment of pulmonary diseases.


Objectives: The aim of this study is to correlate e-Lung measures, an AI-based software for HRCT image assessment, with current standard measures of pulmonary involvement used in the routine care of SSc-ILD patients.


Methods: e-Lung software (Brainomix Ltd, UK) was applied to baseline HRCT images of consecutive SSc-ILD patients. Measures of total lung volumes (TLV), percentage of ground-glass opacities (GGO%), percentage of abnormal lung (AL%), and (weighted) reticulo-vascular score (RVS-WRVS) reflecting the severity of reticular and vascular changes were derived.


Results: A total of 68 patients’ HRCT scans were assessed by e-Lung. Clinical characteristics of the enrolled patients are reported in Table 1. Forced vital capacity (FVC) showed a moderate positive correlation with TLV (Rs=0.44, p<0.001) and moderate negative correlations with GGO% (Rs-0.47, p<0.001), AL% (Rs=-0.63, p<0.001), and WRVS (Rs=-0.66, p<0.001). Alveolar diffusion of carbon monoxide (DLCO) showed a moderate positive correlation with TLV (Rs=0.41, p=0.001), AL% (Rs=-0.46, p<0.001), and WRVS (Rs=-0.55, p<0.001), and a weak negative correlation with GGO% (Rs=-0.27, p=0.039). Finally, higher median WRVS values were reported in the subgroup patients with pulmonary artery systolic pressure ≥40 mmHg on heart ultrasound [8.73 (IQR 7.21-15.50) vs 7.3 (IQR 5.24-10.61), p=0.032] or with mean pulmonary artery pressure ≥25 mmHg on right heart catheterization [14.01 (IQR 7.21-19.19) vs 7.48 (IQR 5.36-10.22), p=0.012] compared to the rest of the patients.


Conclusion: e-Lung assessment was feasible in SSc-ILD patients and provided AI-derived measures from HRCT images that correlated with FVC and DLCO. WRVS was also higher in patients with pulmonary hypertension. AI could integrate current measures of assessment for pulmonary complications in SSc patients.

Characteristics of the patients

N = 68
Age, yrs, mean±SD 53.1±12.7
Male 16 (23.5%)
Disease duration, yrs, median (IQR ) 4.0 (1.0, 9.0)
LeRoy diffuse 44 (64.7%)
ACA positive 6 (8.8%)
ATA positive 35 (51.5%)
ARPIIIA positive 9 (15.8%)
Late capillaroscopy pattern 20 (45.5%)
Baseline FVC (% ) 86.8±22.4
Baseline DLCO (% ) 52.7±13.3
PH on RHC 13 (19.1%)
PASP>40 mmHg 18 (26.5%)
Digital Ulcers 36 (52.9%)
Telangiectasias 37 (54.4%)
ELung Lung Volume, ml, mean±SD 3,688.1 (2,848.6, 4,391.4)
Elung GGO, %, mean±SD 6.4 (3.3, 13.5)
ELung WRVS, mean±SD 8.1 (5.5, 12.1)

ACA - Anti-Centromere Antibody, ARPIIIA - Anti-RNA Polymerase III Antibody, ATA - Anti-Topoisomerase Antibody, DLCO - Alveolar Diffusion of Carbon Monoxide, FVC - Forced Vital Capacity, GGO - Ground Glass Opacities, IQR - Interquartile Range, PAPS - Pulmonary Artery Systolic Pressure, PH - Pulmonary Hypertension, RHC - Right Heart Catheterization, SD - Standard Deviations, WRVS - Weighted Reticulo Vascular Score


REFERENCES: NIL.


Acknowledgements: NIL.


Disclosure of Interests: Lucy Thornton: None declared, Enrico De Lorenzis: None declared, Stefano Di Donato: None declared, Marco Minerba: None declared, Lesley-Anne Bissell Abbvie, Alfasigma, Alfasigma, Peter George stock options at Brainomix, Senior medical director at Brainomix, Boehringer Ingelheim, Roche, GSK, AstraZeneca, Daiichi-Sankyo and Avalyn, Francesco Del Galdo AbbVie, Argenx, Arxx, AstraZeneca, Boehringer-Ingelheim, Capella, Chemomab, GSK, Janssen, Mitsubishi-Tanabe, and Novartis, research support from AbbVie, Argenx, Arxx, AstraZeneca, Boehringer-Ingelheim, Capella, Chemomab, GSK, Janssen, Mitsubishi-Tanabe, and Novartis.

© The Authors 2025. This abstract is an open access article published in Annals of Rheumatic Diseases under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ). Neither EULAR nor the publisher make any representation as to the accuracy of the content. The authors are solely responsible for the content in their abstract including accuracy of the facts, statements, results, conclusion, citing resources etc.


DOI: annrheumdis-2025-eular.B3648
Keywords: Lungs, Imaging, Artificial Intelligence
Citation: , volume 84, supplement 1, year 2025, page 2317
Session: Systemic sclerosis (Publication Only)