3D Segmentation of Multi-contrast Cardiac Magnetic Resonances With Topological Correction and Synthetic Data Augmentation
Financiación H2020 / H2020 Funds
Resumen: Purpose: Automatic segmentation of cardiac magnetic resonance (CMR) images improves the evaluation of heart structure and function, helping clinical diagnosis and the generation of in silico models. Recent advances have introduced synthetic augmentation (SA) using generative adversarial networks (GANs) and topological correction (TC) via persistent homology to enhance segmentation with convolutional neural networks (CNNs). However, their combined effectiveness remains unexplored. Here, we extend and systematically evaluate these techniques, individually and in combination, for the first time in the context of three-dimensional (3D) CMR segmentation across challenging multi-vendor, multi-center, multi-class, and multi-contrast data sets. Methods: Data involved anisotropic, topologically inconsistent cine and late gadolinium-enhanced (LGE) CMRs, and isotropic, topologically consistent ex vivo CMRs. Topological priors were defined in each data set from ground truth label (GTL) assessments, and TC was applied by retraining the baseline 3D CNN with a loss function accounting for topological discrepancies. For SA, deformed GTLs were used to generate synthetic images using trained 3D GANs. Results: Consistent segmentation improvements were observed for the ex vivo data in both overlap with GTLs and topological precision when applying TC and SA individually and in combination. Notably, an enhanced identification of the infarction was obtained when SA and TC were used in the LGE data. Overall, SA increased the predictions overlap with GTLs, while TC reduced the topological discrepancies across all data sets. Conclusion: TC and SA demonstrate strong potential for improving 3D CMR segmentation on complex, real-world data sets, especially when topologically consistent data are available for training.
Idioma: Inglés
DOI: 10.1007/s10439-026-04115-8
Año: 2026
Publicado en: Annals of Biomedical Engineering (2026), [18 pp.]
ISSN: 0090-6964

Financiación: info:eu-repo/grantAgreement/ES/DGA/LMP97_21
Financiación: info:eu-repo/grantAgreement/ES/DGA/T39-23R
Financiación: info:eu-repo/grantAgreement/EC/H2020/638284/EU/Is your heart aging well? A systems biology approach to characterize cardiac aging from the cell to the body surface/MODELAGE
Financiación: info:eu-repo/grantAgreement/EC/H2020/874827/EU/Computational biomechanics and bioengineering 3D printing to develop a personalized regenerative biological ventricular assist device to provide lasting functional support to damaged hearts/BRAV3
Financiación: info:eu-repo/grantAgreement/ES/MCIN/PLEC2021-008127
Financiación: info:eu-repo/grantAgreement/ES/MICINN/PID2022-1405560B-I00
Financiación: info:eu-repo/grantAgreement/EUR/MICINN/TED2021-130459B-I00
Tipo y forma: Artículo (Versión definitiva)
Área (Departamento): Área Teoría Señal y Comunicac. (Dpto. Ingeniería Electrón.Com.)
Área (Departamento): Área Mec.Med.Cont. y Teor.Est. (Dpto. Ingeniería Mecánica)


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Exportado de SIDERAL (2026-05-05-13:36:33)


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Este artículo se encuentra en las siguientes colecciones:
Artículos > Artículos por área > Mec. de Medios Contínuos y Teor. de Estructuras
Artículos > Artículos por área > Teoría de la Señal y Comunicaciones



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