AirMorph: Topology-Preserving Deep Learning for Pulmonary Airway Analysis

• URL: http://arxiv.org/abs/2412.11039v2
• Date: Thu, 08 May 2025 14:24:13 GMT
• Title: AirMorph: Topology-Preserving Deep Learning for Pulmonary Airway Analysis
• Authors: Minghui Zhang, Chenyu Li, Fangfang Xie, Yaoyu Liu, Hanxiao Zhang, Junyang Wu, Chunxi Zhang, Jie Yang, Jiayuan Sun, Guang-Zhong Yang, Yun Gu,
• Abstract summary: We introduce AirMorph, a robust, end-to-end deep learning pipeline enabling fully automatic and comprehensive airway anatomical labeling at lobar, segmental, and subsegmental resolutions.<n>AirMorph consistently outperformed existing segmentation and labeling methods in terms of accuracy, topological consistency, and completeness.<n>It demonstrates strong discriminative power, revealing disease-specific morphological patterns with high interpretability and explainability.
• Score: 33.17242610567077
• License: http://creativecommons.org/licenses/by/4.0/
• Abstract: Accurate anatomical labeling and analysis of the pulmonary structure and its surrounding anatomy from thoracic CT is getting increasingly important for understanding the etilogy of abnormalities or supporting targetted therapy and early interventions. Whilst lung and airway cell atlases have been attempted, there is a lack of fine-grained morphological atlases that are clinically deployable. In this work, we introduce AirMorph, a robust, end-to-end deep learning pipeline enabling fully automatic and comprehensive airway anatomical labeling at lobar, segmental, and subsegmental resolutions that can be used to create digital atlases of the lung. Evaluated across large-scale multi-center datasets comprising diverse pulmonary conditions, the AirMorph consistently outperformed existing segmentation and labeling methods in terms of accuracy, topological consistency, and completeness. To simplify clinical interpretation, we further introduce a compact anatomical signature quantifying critical morphological airway features, including stenosis, ectasia, tortuosity, divergence, length, and complexity. When applied to various pulmonary diseases such as pulmonary fibrosis, emphysema, atelectasis, consolidation, and reticular opacities, it demonstrates strong discriminative power, revealing disease-specific morphological patterns with high interpretability and explainability. Additionally, AirMorph supports efficient automated branching pattern analysis, potentially enhancing bronchoscopic navigation planning and procedural safety, offering a valuable clinical tool for improved diagnosis, targeted treatment, and personalized patient care.

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