TY - JOUR
T1 - Interpretable cardiac anatomy modeling using variational mesh autoencoders
AU - Beetz, Marcel
AU - Corral Acero, Jorge
AU - Banerjee, Abhirup
AU - Eitel, Ingo
AU - Zacur, Ernesto
AU - Lange, Torben
AU - Stiermaier, Thomas
AU - Evertz, Ruben
AU - Backhaus, Sören J.
AU - Thiele, Holger
AU - Bueno-Orovio, Alfonso
AU - Lamata, Pablo
AU - Schuster, Andreas
AU - Grau, Vicente
N1 - Publisher Copyright:
Copyright © 2022 Beetz, Corral Acero, Banerjee, Eitel, Zacur, Lange, Stiermaier, Evertz, Backhaus, Thiele, Bueno-Orovio, Lamata, Schuster and Grau.
PY - 2022/12/22
Y1 - 2022/12/22
N2 - Cardiac anatomy and function vary considerably across the human population with important implications for clinical diagnosis and treatment planning. Consequently, many computer-based approaches have been developed to capture this variability for a wide range of applications, including explainable cardiac disease detection and prediction, dimensionality reduction, cardiac shape analysis, and the generation of virtual heart populations. In this work, we propose a variational mesh autoencoder (mesh VAE) as a novel geometric deep learning approach to model such population-wide variations in cardiac shapes. It embeds multi-scale graph convolutions and mesh pooling layers in a hierarchical VAE framework to enable direct processing of surface mesh representations of the cardiac anatomy in an efficient manner. The proposed mesh VAE achieves low reconstruction errors on a dataset of 3D cardiac meshes from over 1,000 patients with acute myocardial infarction, with mean surface distances between input and reconstructed meshes below the underlying image resolution. We also find that it outperforms a voxelgrid-based deep learning benchmark in terms of both mean surface distance and Hausdorff distance while requiring considerably less memory. Furthermore, we explore the quality and interpretability of the mesh VAE's latent space and showcase its ability to improve the prediction of major adverse cardiac events over a clinical benchmark. Finally, we investigate the method's ability to generate realistic virtual populations of cardiac anatomies and find good alignment between the synthesized and gold standard mesh populations in terms of multiple clinical metrics.
AB - Cardiac anatomy and function vary considerably across the human population with important implications for clinical diagnosis and treatment planning. Consequently, many computer-based approaches have been developed to capture this variability for a wide range of applications, including explainable cardiac disease detection and prediction, dimensionality reduction, cardiac shape analysis, and the generation of virtual heart populations. In this work, we propose a variational mesh autoencoder (mesh VAE) as a novel geometric deep learning approach to model such population-wide variations in cardiac shapes. It embeds multi-scale graph convolutions and mesh pooling layers in a hierarchical VAE framework to enable direct processing of surface mesh representations of the cardiac anatomy in an efficient manner. The proposed mesh VAE achieves low reconstruction errors on a dataset of 3D cardiac meshes from over 1,000 patients with acute myocardial infarction, with mean surface distances between input and reconstructed meshes below the underlying image resolution. We also find that it outperforms a voxelgrid-based deep learning benchmark in terms of both mean surface distance and Hausdorff distance while requiring considerably less memory. Furthermore, we explore the quality and interpretability of the mesh VAE's latent space and showcase its ability to improve the prediction of major adverse cardiac events over a clinical benchmark. Finally, we investigate the method's ability to generate realistic virtual populations of cardiac anatomies and find good alignment between the synthesized and gold standard mesh populations in terms of multiple clinical metrics.
UR - http://www.scopus.com/inward/record.url?scp=85145739837&partnerID=8YFLogxK
U2 - 10.3389/fcvm.2022.983868
DO - 10.3389/fcvm.2022.983868
M3 - Journal articles
AN - SCOPUS:85145739837
SN - 2297-055X
VL - 9
JO - Frontiers in Cardiovascular Medicine
JF - Frontiers in Cardiovascular Medicine
M1 - 983868
ER -