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Model order reduction for left ventricular mechanics via congruency training
Computational models of the cardiovascular system and specifically heart function are currently being investigated as analytic tools to assist medical practice and clinical trials. To achieve clinical utility, models should be able to assimilate the diagnostic multi-modality data available for each...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944464/ https://www.ncbi.nlm.nih.gov/pubmed/31905197 http://dx.doi.org/10.1371/journal.pone.0219876 |
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author | Di Achille, Paolo Parikh, Jaimit Khamzin, Svyatoslav Solovyova, Olga Kozloski, James Gurev, Viatcheslav |
author_facet | Di Achille, Paolo Parikh, Jaimit Khamzin, Svyatoslav Solovyova, Olga Kozloski, James Gurev, Viatcheslav |
author_sort | Di Achille, Paolo |
collection | PubMed |
description | Computational models of the cardiovascular system and specifically heart function are currently being investigated as analytic tools to assist medical practice and clinical trials. To achieve clinical utility, models should be able to assimilate the diagnostic multi-modality data available for each patient and generate consistent representations of the underlying cardiovascular physiology. While finite element models of the heart can naturally account for patient-specific anatomies reconstructed from medical images, optimizing the many other parameters driving simulated cardiac functions is challenging due to computational complexity. With the goal of streamlining parameter adaptation, in this paper we present a novel, multifidelity strategy for model order reduction of 3-D finite element models of ventricular mechanics. Our approach is centered around well established findings on the similarity between contraction of an isolated muscle and the whole ventricle. Specifically, we demonstrate that simple linear transformations between sarcomere strain (tension) and ventricular volume (pressure) are sufficient to reproduce global pressure-volume outputs of 3-D finite element models even by a reduced model with just a single myocyte unit. We further develop a procedure for congruency training of a surrogate low-order model from multi-scale finite elements, and we construct an example of parameter optimization based on medical images. We discuss how the presented approach might be employed to process large datasets of medical images as well as databases of echocardiographic reports, paving the way towards application of heart mechanics models in the clinical practice. |
format | Online Article Text |
id | pubmed-6944464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69444642020-01-17 Model order reduction for left ventricular mechanics via congruency training Di Achille, Paolo Parikh, Jaimit Khamzin, Svyatoslav Solovyova, Olga Kozloski, James Gurev, Viatcheslav PLoS One Research Article Computational models of the cardiovascular system and specifically heart function are currently being investigated as analytic tools to assist medical practice and clinical trials. To achieve clinical utility, models should be able to assimilate the diagnostic multi-modality data available for each patient and generate consistent representations of the underlying cardiovascular physiology. While finite element models of the heart can naturally account for patient-specific anatomies reconstructed from medical images, optimizing the many other parameters driving simulated cardiac functions is challenging due to computational complexity. With the goal of streamlining parameter adaptation, in this paper we present a novel, multifidelity strategy for model order reduction of 3-D finite element models of ventricular mechanics. Our approach is centered around well established findings on the similarity between contraction of an isolated muscle and the whole ventricle. Specifically, we demonstrate that simple linear transformations between sarcomere strain (tension) and ventricular volume (pressure) are sufficient to reproduce global pressure-volume outputs of 3-D finite element models even by a reduced model with just a single myocyte unit. We further develop a procedure for congruency training of a surrogate low-order model from multi-scale finite elements, and we construct an example of parameter optimization based on medical images. We discuss how the presented approach might be employed to process large datasets of medical images as well as databases of echocardiographic reports, paving the way towards application of heart mechanics models in the clinical practice. Public Library of Science 2020-01-06 /pmc/articles/PMC6944464/ /pubmed/31905197 http://dx.doi.org/10.1371/journal.pone.0219876 Text en © 2020 Di Achille et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Di Achille, Paolo Parikh, Jaimit Khamzin, Svyatoslav Solovyova, Olga Kozloski, James Gurev, Viatcheslav Model order reduction for left ventricular mechanics via congruency training |
title | Model order reduction for left ventricular mechanics via congruency training |
title_full | Model order reduction for left ventricular mechanics via congruency training |
title_fullStr | Model order reduction for left ventricular mechanics via congruency training |
title_full_unstemmed | Model order reduction for left ventricular mechanics via congruency training |
title_short | Model order reduction for left ventricular mechanics via congruency training |
title_sort | model order reduction for left ventricular mechanics via congruency training |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944464/ https://www.ncbi.nlm.nih.gov/pubmed/31905197 http://dx.doi.org/10.1371/journal.pone.0219876 |
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