Cardiac mesh morphing method for finite element modeling of heart failure with preserved ejection fraction.

Cardiac magnetic resonance imaging (cMRI) Cardiac modeling Finite element Heart failure with preserved ejection fraction (HFpEF) Mesh-morphing

Journal

Journal of the mechanical behavior of biomedical materials
ISSN: 1878-0180
Titre abrégé: J Mech Behav Biomed Mater
Pays: Netherlands
ID NLM: 101322406

Informations de publication

Date de publication:
02 2022
Historique:
received: 19 09 2021
revised: 21 10 2021
accepted: 24 10 2021
pubmed: 4 1 2022
medline: 1 2 2022
entrez: 3 1 2022
Statut: ppublish

Résumé

Numerical modeling of heart biomechanics can realistically capture morphological variations in diseases and has been helpful in advancing our understanding of the physiology. Subject-specific models require anatomic representation of medical images, and it is desirable to have a consistently repeatable models for any given morphology. In this study, we propose a novel and easily adaptable cardiac reconstruction algorithm by morphing an existing discretized mesh of an advanced finite element (FE) model, to match anatomies acquired from porcine cardiac magnetic resonance imaging (cMRI) scans. The morphing algorithm involves iterative FE simulations with visco-hyperelastic material properties. The living heart porcine model (LHPM) was chosen as the input baseline FE mesh, in order to preserve detailed anatomical features that cannot be captured in routine scans such as myofiber orientations and conduction pathways. The algorithm was demonstrated for the recreation of porcine hearts of a healthy subject and of a subject induced with heart failure with preserved ejection fraction (HFpEF) conditions, where there were substantial hypertrophy and anatomical alterations. We further used the morphed meshes for FE modeling of cardiac contraction and relaxation, thus demonstrating the applicability of the proposed algorithm in producing viable meshes. The results show that our algorithm can recreate the characteristic anatomical changes of cardiac remodeling, including heart muscle thickening, as well as replicate the reduction in ventricular volume. This algorithm allows for the creation of subject-specific models with the same mesh connectivity, thus enabling spatial comparison and analysis of pathologic progress.

Identifiants

pubmed: 34979481
pii: S1751-6161(21)00568-3
doi: 10.1016/j.jmbbm.2021.104937
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104937

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Jonathan Weissmann (J)

Department of Biomedical Engineering, Tel Aviv University, Israel.

Christopher J Charles (CJ)

Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Cardiovascular Research Institute, National University of Singapore, Singapore; Christchurch Heart Institute, Department of Medicine, University of Otago, Christchurch, New Zealand.

A Mark Richards (AM)

Cardiovascular Research Institute, National University of Singapore, Singapore; Christchurch Heart Institute, Department of Medicine, University of Otago, Christchurch, New Zealand.

Choon Hwai Yap (CH)

Department of Bioengineering, Imperial College London, UK.

Gil Marom (G)

School of Mechanical Engineering, Tel Aviv University, Israel. Electronic address: maromgil@tau.ac.il.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell

Selecting optimal software code descriptors-The case of Java.

Yegor Bugayenko, Zamira Kholmatova, Artem Kruglov et al.
1.00
Software Algorithms Programming Languages
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice

Classifications MeSH