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Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort
This paper presents a morphological analysis of fibrotic scarring in non-ischemic dilated cardiomyopathy, and its relationship to electrical instabilities which underlie reentrant arrhythmias. Two dimensional electrophysiological simulation models were constructed from a set of 699 late gadolinium e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837623/ https://www.ncbi.nlm.nih.gov/pubmed/31658247 http://dx.doi.org/10.1371/journal.pcbi.1007421 |
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author | Balaban, Gabriel Halliday, Brian P. Bai, Wenjia Porter, Bradley Malvuccio, Carlotta Lamata, Pablo Rinaldi, Christopher A. Plank, Gernot Rueckert, Daniel Prasad, Sanjay K. Bishop, Martin J. |
author_facet | Balaban, Gabriel Halliday, Brian P. Bai, Wenjia Porter, Bradley Malvuccio, Carlotta Lamata, Pablo Rinaldi, Christopher A. Plank, Gernot Rueckert, Daniel Prasad, Sanjay K. Bishop, Martin J. |
author_sort | Balaban, Gabriel |
collection | PubMed |
description | This paper presents a morphological analysis of fibrotic scarring in non-ischemic dilated cardiomyopathy, and its relationship to electrical instabilities which underlie reentrant arrhythmias. Two dimensional electrophysiological simulation models were constructed from a set of 699 late gadolinium enhanced cardiac magnetic resonance images originating from 157 patients. Areas of late gadolinium enhancement (LGE) in each image were assigned one of 10 possible microstructures, which modelled the details of fibrotic scarring an order of magnitude below the MRI scan resolution. A simulated programmed electrical stimulation protocol tested each model for the possibility of generating either a transmural block or a transmural reentry. The outcomes of the simulations were compared against morphological LGE features extracted from the images. Models which blocked or reentered, grouped by microstructure, were significantly different from one another in myocardial-LGE interface length, number of components and entropy, but not in relative area and transmurality. With an unknown microstructure, transmurality alone was the best predictor of block, whereas a combination of interface length, transmurality and number of components was the best predictor of reentry in linear discriminant analysis. |
format | Online Article Text |
id | pubmed-6837623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68376232019-11-12 Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort Balaban, Gabriel Halliday, Brian P. Bai, Wenjia Porter, Bradley Malvuccio, Carlotta Lamata, Pablo Rinaldi, Christopher A. Plank, Gernot Rueckert, Daniel Prasad, Sanjay K. Bishop, Martin J. PLoS Comput Biol Research Article This paper presents a morphological analysis of fibrotic scarring in non-ischemic dilated cardiomyopathy, and its relationship to electrical instabilities which underlie reentrant arrhythmias. Two dimensional electrophysiological simulation models were constructed from a set of 699 late gadolinium enhanced cardiac magnetic resonance images originating from 157 patients. Areas of late gadolinium enhancement (LGE) in each image were assigned one of 10 possible microstructures, which modelled the details of fibrotic scarring an order of magnitude below the MRI scan resolution. A simulated programmed electrical stimulation protocol tested each model for the possibility of generating either a transmural block or a transmural reentry. The outcomes of the simulations were compared against morphological LGE features extracted from the images. Models which blocked or reentered, grouped by microstructure, were significantly different from one another in myocardial-LGE interface length, number of components and entropy, but not in relative area and transmurality. With an unknown microstructure, transmurality alone was the best predictor of block, whereas a combination of interface length, transmurality and number of components was the best predictor of reentry in linear discriminant analysis. Public Library of Science 2019-10-28 /pmc/articles/PMC6837623/ /pubmed/31658247 http://dx.doi.org/10.1371/journal.pcbi.1007421 Text en © 2019 Balaban 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 Balaban, Gabriel Halliday, Brian P. Bai, Wenjia Porter, Bradley Malvuccio, Carlotta Lamata, Pablo Rinaldi, Christopher A. Plank, Gernot Rueckert, Daniel Prasad, Sanjay K. Bishop, Martin J. Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title | Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title_full | Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title_fullStr | Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title_full_unstemmed | Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title_short | Scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
title_sort | scar shape analysis and simulated electrical instabilities in a non-ischemic dilated cardiomyopathy patient cohort |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837623/ https://www.ncbi.nlm.nih.gov/pubmed/31658247 http://dx.doi.org/10.1371/journal.pcbi.1007421 |
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