Background: Cardiovascular disease is a leading cause of mortality, with coronary artery disease accounting for over 60% of cases in adults. Accurate quantification of coronary stenosis in forensic autopsies is crucial for determining causality between pathological findings and death, but is hindered by subjective visual assessments and inter-observer variability. This study aimed to develop an AI-driven tool using whole-slide images for objective stenosis measurement in forensic investigations. Materials and methods: From 98 anonymized H&E-stained autopsy slides (234 coronary sections), 103 high-quality regions of interest were selected and split into training (n = 82), validation (n = 14), and test (n = 7) datasets. Annotations delineated lumen, internal elastic lamina, and external elastic lamina using QuPath. A SegFormer-B0 transformer model was trained with data augmentation, weighted cross-entropy loss, and AdamW optimization. Post-processing enforced anatomical structural hierarchy and generated hybrid confidence maps. Results: On validation dataset, agreement with ground truth was excellent (MAE 3.22% points; RMSE 4.00; MAPE 6.07%; r = 0.986; ICC = 0.986), with slight underestimation. Bland–Altman bias was − 1.36 pp (95% LoA − 9.01 to 6.28 pp), indicating performance across severities. On the test set, accuracy improved (MAE 1.01 pp; RMSE 1.50; MAPE 2.11%; r = 0.998; ICC = 0.995) and outperformed three pathologists’ visual estimates (MAE 16.11, 8.18, 4.79 pp). Bland–Altman bias for the model was − 0.82 pp with tight limits of agreement (− 3.48 to 1.83 pp). Total inference time was 199.08 s for seven cases (28.44 s/image). Conclusions: WSI-based transformer pipeline enables rapid, auditable, and reproducible coronary stenosis measurement, reducing inter-observer variability and supporting standardized interpretation in forensic investigations.

Development of a deep learning-based tool for coronary artery stenosis evaluation in forensic autopsies using whole slide imaging

Chighine A.;D'Aloja E.;Brunelli M.;
2026-01-01

Abstract

Background: Cardiovascular disease is a leading cause of mortality, with coronary artery disease accounting for over 60% of cases in adults. Accurate quantification of coronary stenosis in forensic autopsies is crucial for determining causality between pathological findings and death, but is hindered by subjective visual assessments and inter-observer variability. This study aimed to develop an AI-driven tool using whole-slide images for objective stenosis measurement in forensic investigations. Materials and methods: From 98 anonymized H&E-stained autopsy slides (234 coronary sections), 103 high-quality regions of interest were selected and split into training (n = 82), validation (n = 14), and test (n = 7) datasets. Annotations delineated lumen, internal elastic lamina, and external elastic lamina using QuPath. A SegFormer-B0 transformer model was trained with data augmentation, weighted cross-entropy loss, and AdamW optimization. Post-processing enforced anatomical structural hierarchy and generated hybrid confidence maps. Results: On validation dataset, agreement with ground truth was excellent (MAE 3.22% points; RMSE 4.00; MAPE 6.07%; r = 0.986; ICC = 0.986), with slight underestimation. Bland–Altman bias was − 1.36 pp (95% LoA − 9.01 to 6.28 pp), indicating performance across severities. On the test set, accuracy improved (MAE 1.01 pp; RMSE 1.50; MAPE 2.11%; r = 0.998; ICC = 0.995) and outperformed three pathologists’ visual estimates (MAE 16.11, 8.18, 4.79 pp). Bland–Altman bias for the model was − 0.82 pp with tight limits of agreement (− 3.48 to 1.83 pp). Total inference time was 199.08 s for seven cases (28.44 s/image). Conclusions: WSI-based transformer pipeline enables rapid, auditable, and reproducible coronary stenosis measurement, reducing inter-observer variability and supporting standardized interpretation in forensic investigations.
2026
Artificial intelligence
Cardiovascular pathology
Coronary stenosis
Digital pathology
Forensic pathology
Whole slide images
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/493685
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