Deep learning-based detection of murine congenital heart defects from µCT scans

Micro-computed tomography (μCT) provides 3D images of congenital heart defects (CHD) in mice. However, diagnosing CHD from μCT scans is time-consuming and requires clinical expertise. Here, we present a deep learning approach to automatically segment and screen normal from malformed hearts. On a cohort of 139 μCT scans of control and mutant mice, our diagnosis model achieves an area-under-the-curve (AUC) of 97%. For further validation, we acquired two additional cohorts after model training. Performance on a similar 'prospective' cohort is excellent (AUC: 100%). Performance on a 'divergent' cohort containing novel genotypes is moderate (AUC: 81%), but improves markedly after model finetuning (AUC: 91%), showcasing robustness and adaptability to technical and biological differences in the data. A user-friendly Napari plugin allows researchers without coding expertise to utilize and retrain the model. Our pipeline will accelerate diagnosis of heart anomalies in mice and facilitate mechanistic studies of CHD.

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Publication Details

Journal
Communications Biology
Published
2025-12-23
DOI
https://doi.org/10.1038/s42003-025-09023-6
Citations
1
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.81

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article

Deep learning-based detection of murine congenital heart defects from µCT scans

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1 citations
Communications Biology
Congenital heart defects research
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article

Deep learning-based detection of murine congenital heart defects from µCT scans

Vanessa Benhamo, Ségolène Bernheim, Amaia Ochandorena-Saa, Audrey Desgrange, Sigolène M. Meilhac, Hoa Nguyen, Lucile Houyel, Christophe Zimmer
article en
1 citations

Abstract

Micro-computed tomography (μCT) provides 3D images of congenital heart defects (CHD) in mice. However, diagnosing CHD from μCT scans is time-consuming and requires clinical expertise. Here, we present a deep learning approach to automatically segment and screen normal from malformed hearts. On a cohort of 139 μCT scans of control and mutant mice, our diagnosis model achieves an area-under-the-curve (AUC) of 97%. For further validation, we acquired two additional cohorts after model training. Performance on a similar 'prospective' cohort is excellent (AUC: 100%). Performance on a 'divergent' cohort containing novel genotypes is moderate (AUC: 81%), but improves markedly after model finetuning (AUC: 91%), showcasing robustness and adaptability to technical and biological differences in the data. A user-friendly Napari plugin allows researchers without coding expertise to utilize and retrain the model. Our pipeline will accelerate diagnosis of heart anomalies in mice and facilitate mechanistic studies of CHD.

Communications BiologyVol. 8(1)
Hôpital Necker-Enfants Malades (FR), Inserm (FR), Institut Pasteur (FR), Université Paris Cité (FR), University of Würzburg (DE), Sanofi (France) (FR), Assistance Publique – Hôpitaux de Paris (FR), Institut des Maladies Génétiques Imagine (FR)
Sanofi, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Institut National Du Cancer, Julius-Maximilians-Universität Würzburg
Openalex Percentile: Top 20%
Congenital heart defects research
0.81
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