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Updated: Sep 9, 2025

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models
Published on: June 20, 2025
Automated quantification of lung pathology on micro-CT in diverse disease models using deep learning
Flore Belmans1, Laura Seldeslachts2, Eliane Vanhoffelen2
1Department of Imaging and Pathology, KU Leuven, Leuven, Belgium; Radiomics.bio, Liège, Belgium.
A new deep learning model efficiently analyzes micro-CT scans of rodent lungs, improving disease tracking and treatment response assessment in preclinical studies. This automated lung segmentation accelerates research for respiratory diseases.
Area of Science:
- * Biomedical imaging
- * Computational pathology
- * Preclinical research
Background:
- * Micro-computed tomography (micro-CT) is crucial for respiratory disease research, enhancing study efficiency and translatability to human trials.
- * Analyzing large micro-CT datasets is a significant bottleneck in preclinical respiratory disease research.
- * Current methods limit the efficient analysis of micro-CT data for longitudinal studies.
Purpose of the Study:
- * To develop a generic deep learning (DL) model for automated lung segmentation in rodent micro-CT images.
- * To assess the generalisability of the DL model across various lung pathologies, disease models, and scanner configurations.
- * To enable efficient and accurate quantification of lung pathology in preclinical respiratory disease studies.
Main Methods:
- * A deep learning (DL) based lung segmentation model was developed using longitudinal micro-CT images from diverse rodent studies.
- * 2D models were trained on axial, coronal, and sagittal slices, with predictions combined into a 2.5D model.
- * Model generalisability was tested on various studies (COVID-19, inflammation, fibrosis), rodent species, and scanner configurations, including public databases.
Main Results:
- * The 2.5D probability averaging DL model achieved a high mean Dice Similarity Coefficient (DSC) of 0.953 ± 0.023 on internal validation data.
- * The models demonstrated strong generalisability, with average DSC values from 0.89 to 0.94 across different conditions.
- * Biomarkers from automated segmentation closely agreed with manual segmentation, validating the model's ability to monitor disease progression and treatment response.
Conclusions:
- * The developed DL pipeline provides efficient analysis of large micro-CT datasets for lung pathology quantification.
- * The model is widely applicable across rodent disease models and various acquisition protocols.
- * This approach enables real-time insights into therapeutic efficacy in preclinical respiratory research.
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