ArticleJournal of thoracic disease2025
A computed tomography-based lung radiomics nomogram to identify acute exacerbation of chronic obstructive pulmonary disease: a multi-institutional validation study.
Article in Journal of thoracic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Predicting the progression risk of chronic obstructive pulmonary disease in high-risk individuals based on whole-lung radiomics and deep learning: a multicenter study.Journal of thoracic disease · 2026Article
- Automated identification of chronic obstructive pulmonary disease and asthma using impulse oscillometry combined with quantitative computed tomography parameters and radiomics features.Journal of thoracic disease · 2026Article
- Radiomics differences between GOLD I-II and GOLD III-IV in patients with chronic obstructive pulmonary disease.Journal of thoracic disease · 2026Article
- Beyond pathogens: a narrative review of the immunological nexus of damage-associated molecular patterns and inflammasome activation in sterile AECOPD.Frontiers in immunology · 2026Review
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Authors and funding
11 authors.
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Abstract
Background: Diagnosing acute exacerbation of chronic obstructive pulmonary disease (AECOPD) remains challenging in clinical practice. Computed tomography (CT) plays a great role in characterizing and quantifying changes in lung structure and function of AECOPD. This study aimed to explore the performance of CT-based whole-lung radiomics in identifying AECOPD. Methods: From 2013 to 2022, 475 chronic obstructive pulmonary disease (COPD) patients were retrospectively enrolled from three hospitals, including 257 non-AECOPD and 218 AECOPD. Whole-lung imaging features were extracted. Eleven machine learning (ML) algorithms were utilized to construct the AECOPD identification model. Least absolute shrinkage and selection operator logistic regression (LR) was applied for feature selection and radiomic signature construction. A radiomic nomogram was then established by combining the radiomic score and clinical factors. Receiver operating characteristic curve analysis and decision curve analysis assessed the predictive performance of the radiomic nomogram in the training, internal, and independent external validation cohorts. Results: Sixty-one radiomic features were collected to construct a radiomic score model. Among the 11 ML algorithms, the LR model achieved the best diagnostic performance, with the area under the curve (AUC) values of 0.974, 0.836, and 0.944 in the training, internal, and external validation sets, respectively. The diagnostic performance surpassed that of the clinical model, with AUC values of 0.630, 0.636, and 0.734 in the respective sets. Notably, the AECOPD radiomic nomogram demonstrated nearly equivalent diagnostic performance to the radiomic score model. The AUC values for the radiomic nomogram were 0.974 in the training set, 0.849 in the internal validation set, and 0.957 in the external validation set. Conclusions: The CT-based whole-lung radiomic nomogram accurately identifies AECOPD and offers a robust tool for clinical diagnosis and treatment planning.
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