Deep Learning-Based Airway Segmentation in Systemic Lupus Erythematosus Patients with Interstitial Lung Disease (SLE-ILD): A Comparative High-Resolution CT Analysis
Sirong Piao (1), Ying Ming (1), Ruijie Zhao (1), Jiaru Wang (1), Ran Xiao (1), Rui Zhao (1), Zicheng Liao (1), Qiqi Xu (2), Shaoze Luo (2), Bing Li (2), Lin Li (2), Zhuangfei Ma (3), Fuling Zheng (1), Wei Song (1) ((1) Department of Radiology

TL;DR
This study develops a deep learning method to automatically segment airways in high-resolution CT scans, revealing significant airway dilation in SLE-ILD patients, aiding early detection and personalized management.
Contribution
A novel deep learning framework based on U-Net architecture for automated airway segmentation in SLE-ILD patients using HRCT scans.
Findings
Significant airway volume enlargement in upper lobes of SLE-ILD patients.
Region-specific airway dilation patterns identified, especially in upper lung zones.
Automated segmentation effectively quantifies airway structural changes.
Abstract
To characterize lobar and segmental airway volume differences between systemic lupus erythematosus (SLE) patients with interstitial lung disease (ILD) and those without ILD (non-ILD) using a deep learning-based approach on non-contrast chest high-resolution CT (HRCT). Methods: A retrospective analysis was conducted on 106 SLE patients (27 SLE-ILD, 79 SLE-non-ILD) who underwent HRCT. A customized deep learning framework based on the U-Net architecture was developed to automatically segment airway structures at the lobar and segmental levels via HRCT. Volumetric measurements of lung lobes and segments derived from the segmentations were statistically compared between the two groups using two-sample t-tests (significance threshold: p < 0.05). Results: At lobar level, significant airway volume enlargement in SLE-ILD patients was observed in the right upper lobe (p=0.009) and left upper lobe…
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Taxonomy
TopicsSystemic Lupus Erythematosus Research · Systemic Sclerosis and Related Diseases · Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
