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Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study

Patient-specific models of the ventricular myocardium, combined with the computational power to run rapid simulations, are approaching the level where they could be used for personalized cardiovascular medicine. A major remaining challenge is determining model parameters from available patient data,...

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Autores principales: Cranford, Jonathan P., O’Hara, Thomas J., Villongco, Christopher T., Hafez, Omar M., Blake, Robert C., Loscalzo, Joseph, Fattebert, Jean-Luc, Richards, David F., Zhang, Xiaohua, Glosli, James N., McCulloch, Andrew D., Krummen, David E., Lightstone, Felice C., Wong, Sergio E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095770/
https://www.ncbi.nlm.nih.gov/pubmed/29549620
http://dx.doi.org/10.1007/s13239-018-0347-0
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author Cranford, Jonathan P.
O’Hara, Thomas J.
Villongco, Christopher T.
Hafez, Omar M.
Blake, Robert C.
Loscalzo, Joseph
Fattebert, Jean-Luc
Richards, David F.
Zhang, Xiaohua
Glosli, James N.
McCulloch, Andrew D.
Krummen, David E.
Lightstone, Felice C.
Wong, Sergio E.
author_facet Cranford, Jonathan P.
O’Hara, Thomas J.
Villongco, Christopher T.
Hafez, Omar M.
Blake, Robert C.
Loscalzo, Joseph
Fattebert, Jean-Luc
Richards, David F.
Zhang, Xiaohua
Glosli, James N.
McCulloch, Andrew D.
Krummen, David E.
Lightstone, Felice C.
Wong, Sergio E.
author_sort Cranford, Jonathan P.
collection PubMed
description Patient-specific models of the ventricular myocardium, combined with the computational power to run rapid simulations, are approaching the level where they could be used for personalized cardiovascular medicine. A major remaining challenge is determining model parameters from available patient data, especially for models of the Purkinje-myocardial junctions (PMJs): the sites of initial ventricular electrical activation. There are no non-invasive methods for localizing PMJs in patients, and the relationship between the standard clinical ECG and PMJ model parameters is underexplored. Thus, this study aimed to determine the sensitivity of the QRS complex of the ECG to the anatomical location and regional number of PMJs. The QRS complex was simulated using an image-based human torso and biventricular model, and cardiac electrophysiology was simulated using Cardioid. The PMJs were modeled as discrete current injection stimuli, and the location and number of stimuli were varied within initial activation regions based on published experiments. Results indicate that the QRS complex features were most sensitive to the presence or absence of four “seed” stimuli, and adjusting locations of nearby “regional” stimuli provided finer tuning. Decreasing number of regional stimuli by an order of magnitude resulted in virtually no change in the QRS complex. Thus, a minimal 12-stimuli configuration was identified that resulted in physiological excitation, defined by QRS complex feature metrics and ventricular excitation pattern. Overall, the sensitivity results suggest that parameterizing PMJ location, rather than number, be given significantly higher priority in future studies creating personalized ventricular models from patient-derived ECGs.
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spelling pubmed-60957702018-08-24 Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study Cranford, Jonathan P. O’Hara, Thomas J. Villongco, Christopher T. Hafez, Omar M. Blake, Robert C. Loscalzo, Joseph Fattebert, Jean-Luc Richards, David F. Zhang, Xiaohua Glosli, James N. McCulloch, Andrew D. Krummen, David E. Lightstone, Felice C. Wong, Sergio E. Cardiovasc Eng Technol Article Patient-specific models of the ventricular myocardium, combined with the computational power to run rapid simulations, are approaching the level where they could be used for personalized cardiovascular medicine. A major remaining challenge is determining model parameters from available patient data, especially for models of the Purkinje-myocardial junctions (PMJs): the sites of initial ventricular electrical activation. There are no non-invasive methods for localizing PMJs in patients, and the relationship between the standard clinical ECG and PMJ model parameters is underexplored. Thus, this study aimed to determine the sensitivity of the QRS complex of the ECG to the anatomical location and regional number of PMJs. The QRS complex was simulated using an image-based human torso and biventricular model, and cardiac electrophysiology was simulated using Cardioid. The PMJs were modeled as discrete current injection stimuli, and the location and number of stimuli were varied within initial activation regions based on published experiments. Results indicate that the QRS complex features were most sensitive to the presence or absence of four “seed” stimuli, and adjusting locations of nearby “regional” stimuli provided finer tuning. Decreasing number of regional stimuli by an order of magnitude resulted in virtually no change in the QRS complex. Thus, a minimal 12-stimuli configuration was identified that resulted in physiological excitation, defined by QRS complex feature metrics and ventricular excitation pattern. Overall, the sensitivity results suggest that parameterizing PMJ location, rather than number, be given significantly higher priority in future studies creating personalized ventricular models from patient-derived ECGs. Springer US 2018-03-16 2018 /pmc/articles/PMC6095770/ /pubmed/29549620 http://dx.doi.org/10.1007/s13239-018-0347-0 Text en © Biomedical Engineering Society 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Cranford, Jonathan P.
O’Hara, Thomas J.
Villongco, Christopher T.
Hafez, Omar M.
Blake, Robert C.
Loscalzo, Joseph
Fattebert, Jean-Luc
Richards, David F.
Zhang, Xiaohua
Glosli, James N.
McCulloch, Andrew D.
Krummen, David E.
Lightstone, Felice C.
Wong, Sergio E.
Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title_full Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title_fullStr Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title_full_unstemmed Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title_short Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study
title_sort efficient computational modeling of human ventricular activation and its electrocardiographic representation: a sensitivity study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095770/
https://www.ncbi.nlm.nih.gov/pubmed/29549620
http://dx.doi.org/10.1007/s13239-018-0347-0
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