Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models

Autores
Gonzalez Martin, Pablo; Sacco, Federica; Butakoff, Constantine; Doste, Ruben; Bederian, Carlos Sergio; Gutierrez Espinosa de los Monteros, Lilian K.; Houzeaux, Guillaume; Iaizzo, Paul A.; Iles, Tinen L.; Vazquez, Mariano; Aguado Sierra, Jazmin
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The aim of this work was to analyze the influence of sex hormones and anatomical details (trabeculations and false tendons) on the electrophysiology of healthy human hearts. Additionally, sex- and anatomy-dependent effects of ventricular tachycardia (VT) inducibility are presented. To this end, four anatomically normal, human, biventricular geometries (two male, two female), with identifiable trabeculations, were obtained from high-resolution, ex-vivo MRI and represented by detailed and smoothed geometrical models (with and without the trabeculations). Additionally one model was augmented by a scar. The electrophysiology finite element model (FEM) simulations were carried out, using O’Hara-Rudy human myocyte model with sex phenotypes of Yang and Clancy. A systematic comparison between detailed vs smooth anatomies, male vs female normal hearts was carried out. The heart with a myocardial infarction was subjected to a programmed stimulus protocol to identify the effects of sex and anatomical detail on ventricular tachycardia inducibility. All female hearts presented QT-interval prolongation however the prolongation interval in comparison to the male phenotypes was anatomy-dependent and was not correlated to the size of the heart. Detailed geometries showed QRS fractionation and increased T-wave magnitude in comparison to the corresponding smoothed geometries. A variety of sustained VTs were obtained in the detailed and smoothed male geometries at different pacing locations, which provide evidence of the geometry-dependent differences regarding the prediction of the locations of reentry channels. In the female phenotype, sustained VTs were induced in both detailed and smooth geometries with RV apex pacing, however no consistent reentry channels were identified. Anatomical and physiological cardiac features play an important role defining risk in cardiac disease. These are often excluded from cardiac electrophysiology simulations. The assumption that the cardiac endocardium is smooth may produce inaccurate predictions towards the location of reentry channels in in-silico tachycardia inducibility studies.
Fil: Gonzalez Martin, Pablo. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Sacco, Federica. Universitat Pompeu Fabra; España. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Butakoff, Constantine. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Doste, Ruben. University of Oxford; Reino Unido
Fil: Bederian, Carlos Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Gutierrez Espinosa de los Monteros, Lilian K.. Instituto de Salud Carlos III; España
Fil: Houzeaux, Guillaume. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Iaizzo, Paul A.. University of Minnesota; Estados Unidos
Fil: Iles, Tinen L.. University of Minnesota; Estados Unidos
Fil: Vazquez, Mariano. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Aguado Sierra, Jazmin. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Materia
Heart
Tachycardia
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/226590

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network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational modelsGonzalez Martin, PabloSacco, FedericaButakoff, ConstantineDoste, RubenBederian, Carlos SergioGutierrez Espinosa de los Monteros, Lilian K.Houzeaux, GuillaumeIaizzo, Paul A.Iles, Tinen L.Vazquez, MarianoAguado Sierra, JazminHeartTachycardiahttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The aim of this work was to analyze the influence of sex hormones and anatomical details (trabeculations and false tendons) on the electrophysiology of healthy human hearts. Additionally, sex- and anatomy-dependent effects of ventricular tachycardia (VT) inducibility are presented. To this end, four anatomically normal, human, biventricular geometries (two male, two female), with identifiable trabeculations, were obtained from high-resolution, ex-vivo MRI and represented by detailed and smoothed geometrical models (with and without the trabeculations). Additionally one model was augmented by a scar. The electrophysiology finite element model (FEM) simulations were carried out, using O’Hara-Rudy human myocyte model with sex phenotypes of Yang and Clancy. A systematic comparison between detailed vs smooth anatomies, male vs female normal hearts was carried out. The heart with a myocardial infarction was subjected to a programmed stimulus protocol to identify the effects of sex and anatomical detail on ventricular tachycardia inducibility. All female hearts presented QT-interval prolongation however the prolongation interval in comparison to the male phenotypes was anatomy-dependent and was not correlated to the size of the heart. Detailed geometries showed QRS fractionation and increased T-wave magnitude in comparison to the corresponding smoothed geometries. A variety of sustained VTs were obtained in the detailed and smoothed male geometries at different pacing locations, which provide evidence of the geometry-dependent differences regarding the prediction of the locations of reentry channels. In the female phenotype, sustained VTs were induced in both detailed and smooth geometries with RV apex pacing, however no consistent reentry channels were identified. Anatomical and physiological cardiac features play an important role defining risk in cardiac disease. These are often excluded from cardiac electrophysiology simulations. The assumption that the cardiac endocardium is smooth may produce inaccurate predictions towards the location of reentry channels in in-silico tachycardia inducibility studies.Fil: Gonzalez Martin, Pablo. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaFil: Sacco, Federica. Universitat Pompeu Fabra; España. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaFil: Butakoff, Constantine. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaFil: Doste, Ruben. University of Oxford; Reino UnidoFil: Bederian, Carlos Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Gutierrez Espinosa de los Monteros, Lilian K.. Instituto de Salud Carlos III; EspañaFil: Houzeaux, Guillaume. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaFil: Iaizzo, Paul A.. University of Minnesota; Estados UnidosFil: Iles, Tinen L.. University of Minnesota; Estados UnidosFil: Vazquez, Mariano. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaFil: Aguado Sierra, Jazmin. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; EspañaPublic Library of Science2023-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/226590Gonzalez Martin, Pablo; Sacco, Federica; Butakoff, Constantine; Doste, Ruben; Bederian, Carlos Sergio; et al.; Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models; Public Library of Science; Plos One; 18; 2-2023; 1-251932-6203CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0263639info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0263639info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:15:14Zoai:ri.conicet.gov.ar:11336/226590instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 12:15:15.25CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
title Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
spellingShingle Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
Gonzalez Martin, Pablo
Heart
Tachycardia
title_short Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
title_full Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
title_fullStr Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
title_full_unstemmed Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
title_sort Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models
dc.creator.none.fl_str_mv Gonzalez Martin, Pablo
Sacco, Federica
Butakoff, Constantine
Doste, Ruben
Bederian, Carlos Sergio
Gutierrez Espinosa de los Monteros, Lilian K.
Houzeaux, Guillaume
Iaizzo, Paul A.
Iles, Tinen L.
Vazquez, Mariano
Aguado Sierra, Jazmin
author Gonzalez Martin, Pablo
author_facet Gonzalez Martin, Pablo
Sacco, Federica
Butakoff, Constantine
Doste, Ruben
Bederian, Carlos Sergio
Gutierrez Espinosa de los Monteros, Lilian K.
Houzeaux, Guillaume
Iaizzo, Paul A.
Iles, Tinen L.
Vazquez, Mariano
Aguado Sierra, Jazmin
author_role author
author2 Sacco, Federica
Butakoff, Constantine
Doste, Ruben
Bederian, Carlos Sergio
Gutierrez Espinosa de los Monteros, Lilian K.
Houzeaux, Guillaume
Iaizzo, Paul A.
Iles, Tinen L.
Vazquez, Mariano
Aguado Sierra, Jazmin
author2_role author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Heart
Tachycardia
topic Heart
Tachycardia
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The aim of this work was to analyze the influence of sex hormones and anatomical details (trabeculations and false tendons) on the electrophysiology of healthy human hearts. Additionally, sex- and anatomy-dependent effects of ventricular tachycardia (VT) inducibility are presented. To this end, four anatomically normal, human, biventricular geometries (two male, two female), with identifiable trabeculations, were obtained from high-resolution, ex-vivo MRI and represented by detailed and smoothed geometrical models (with and without the trabeculations). Additionally one model was augmented by a scar. The electrophysiology finite element model (FEM) simulations were carried out, using O’Hara-Rudy human myocyte model with sex phenotypes of Yang and Clancy. A systematic comparison between detailed vs smooth anatomies, male vs female normal hearts was carried out. The heart with a myocardial infarction was subjected to a programmed stimulus protocol to identify the effects of sex and anatomical detail on ventricular tachycardia inducibility. All female hearts presented QT-interval prolongation however the prolongation interval in comparison to the male phenotypes was anatomy-dependent and was not correlated to the size of the heart. Detailed geometries showed QRS fractionation and increased T-wave magnitude in comparison to the corresponding smoothed geometries. A variety of sustained VTs were obtained in the detailed and smoothed male geometries at different pacing locations, which provide evidence of the geometry-dependent differences regarding the prediction of the locations of reentry channels. In the female phenotype, sustained VTs were induced in both detailed and smooth geometries with RV apex pacing, however no consistent reentry channels were identified. Anatomical and physiological cardiac features play an important role defining risk in cardiac disease. These are often excluded from cardiac electrophysiology simulations. The assumption that the cardiac endocardium is smooth may produce inaccurate predictions towards the location of reentry channels in in-silico tachycardia inducibility studies.
Fil: Gonzalez Martin, Pablo. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Sacco, Federica. Universitat Pompeu Fabra; España. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Butakoff, Constantine. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Doste, Ruben. University of Oxford; Reino Unido
Fil: Bederian, Carlos Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Gutierrez Espinosa de los Monteros, Lilian K.. Instituto de Salud Carlos III; España
Fil: Houzeaux, Guillaume. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Iaizzo, Paul A.. University of Minnesota; Estados Unidos
Fil: Iles, Tinen L.. University of Minnesota; Estados Unidos
Fil: Vazquez, Mariano. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
Fil: Aguado Sierra, Jazmin. Barcelona Supercomputing Center - Centro Nacional de Supercomputacion; España
description The aim of this work was to analyze the influence of sex hormones and anatomical details (trabeculations and false tendons) on the electrophysiology of healthy human hearts. Additionally, sex- and anatomy-dependent effects of ventricular tachycardia (VT) inducibility are presented. To this end, four anatomically normal, human, biventricular geometries (two male, two female), with identifiable trabeculations, were obtained from high-resolution, ex-vivo MRI and represented by detailed and smoothed geometrical models (with and without the trabeculations). Additionally one model was augmented by a scar. The electrophysiology finite element model (FEM) simulations were carried out, using O’Hara-Rudy human myocyte model with sex phenotypes of Yang and Clancy. A systematic comparison between detailed vs smooth anatomies, male vs female normal hearts was carried out. The heart with a myocardial infarction was subjected to a programmed stimulus protocol to identify the effects of sex and anatomical detail on ventricular tachycardia inducibility. All female hearts presented QT-interval prolongation however the prolongation interval in comparison to the male phenotypes was anatomy-dependent and was not correlated to the size of the heart. Detailed geometries showed QRS fractionation and increased T-wave magnitude in comparison to the corresponding smoothed geometries. A variety of sustained VTs were obtained in the detailed and smoothed male geometries at different pacing locations, which provide evidence of the geometry-dependent differences regarding the prediction of the locations of reentry channels. In the female phenotype, sustained VTs were induced in both detailed and smooth geometries with RV apex pacing, however no consistent reentry channels were identified. Anatomical and physiological cardiac features play an important role defining risk in cardiac disease. These are often excluded from cardiac electrophysiology simulations. The assumption that the cardiac endocardium is smooth may produce inaccurate predictions towards the location of reentry channels in in-silico tachycardia inducibility studies.
publishDate 2023
dc.date.none.fl_str_mv 2023-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/226590
Gonzalez Martin, Pablo; Sacco, Federica; Butakoff, Constantine; Doste, Ruben; Bederian, Carlos Sergio; et al.; Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models; Public Library of Science; Plos One; 18; 2-2023; 1-25
1932-6203
CONICET Digital
CONICET
url http://hdl.handle.net/11336/226590
identifier_str_mv Gonzalez Martin, Pablo; Sacco, Federica; Butakoff, Constantine; Doste, Ruben; Bederian, Carlos Sergio; et al.; Ventricular anatomical complexity and sex differences impact predictions from electrophysiological computational models; Public Library of Science; Plos One; 18; 2-2023; 1-25
1932-6203
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0263639
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0263639
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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