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Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts

Transcatheter therapies are emerging for functional mitral regurgitation (FMR) treatment, however there is lack of pathological models for their preclinical assessment. We investigated the applicability of deer hearts for this purpose. 8 whole deer hearts were housed in a pulsatile flow bench. At ba...

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Autores principales: Jaworek, Michal, Mangini, Andrea, Maroncelli, Edoardo, Lucherini, Federico, Rosa, Rubina, Salurso, Eleonora, Votta, Emiliano, Antona, Carlo, Fiore, Gianfranco Beniamino, Vismara, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219575/
https://www.ncbi.nlm.nih.gov/pubmed/32959169
http://dx.doi.org/10.1007/s12265-020-10071-y
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author Jaworek, Michal
Mangini, Andrea
Maroncelli, Edoardo
Lucherini, Federico
Rosa, Rubina
Salurso, Eleonora
Votta, Emiliano
Antona, Carlo
Fiore, Gianfranco Beniamino
Vismara, Riccardo
author_facet Jaworek, Michal
Mangini, Andrea
Maroncelli, Edoardo
Lucherini, Federico
Rosa, Rubina
Salurso, Eleonora
Votta, Emiliano
Antona, Carlo
Fiore, Gianfranco Beniamino
Vismara, Riccardo
author_sort Jaworek, Michal
collection PubMed
description Transcatheter therapies are emerging for functional mitral regurgitation (FMR) treatment, however there is lack of pathological models for their preclinical assessment. We investigated the applicability of deer hearts for this purpose. 8 whole deer hearts were housed in a pulsatile flow bench. At baseline, all mitral valves featured normal coaptation. The pathological state was induced by 60-minutes intraventricular constant pressurization. It caused mitral annulus dilation (antero-posterior diameter increase from 31.8 ± 5.6 mm to 39.5 ± 4.9 mm, p = 0.001), leaflets tethering (maximal tenting height increase from 7.3 ± 2.5 mm to 12.7 ± 3.4 mm, p < 0.001) and left ventricular diameter increase (from 67.8 ± 7.5 mm to 79.4 ± 6.5 mm, p = 0.004). These geometrical reconfigurations led to restricted mitral valve leaflets motion and leaflet coaptation loss. Preliminary feasibility assessment of two FMR treatments was performed in the developed model. Deer hearts showed ability to dilate under constant pressurization and have potential to be used for realistic preclinical research of novel FMR therapies. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12265-020-10071-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-82195752021-06-28 Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts Jaworek, Michal Mangini, Andrea Maroncelli, Edoardo Lucherini, Federico Rosa, Rubina Salurso, Eleonora Votta, Emiliano Antona, Carlo Fiore, Gianfranco Beniamino Vismara, Riccardo J Cardiovasc Transl Res Original Article Transcatheter therapies are emerging for functional mitral regurgitation (FMR) treatment, however there is lack of pathological models for their preclinical assessment. We investigated the applicability of deer hearts for this purpose. 8 whole deer hearts were housed in a pulsatile flow bench. At baseline, all mitral valves featured normal coaptation. The pathological state was induced by 60-minutes intraventricular constant pressurization. It caused mitral annulus dilation (antero-posterior diameter increase from 31.8 ± 5.6 mm to 39.5 ± 4.9 mm, p = 0.001), leaflets tethering (maximal tenting height increase from 7.3 ± 2.5 mm to 12.7 ± 3.4 mm, p < 0.001) and left ventricular diameter increase (from 67.8 ± 7.5 mm to 79.4 ± 6.5 mm, p = 0.004). These geometrical reconfigurations led to restricted mitral valve leaflets motion and leaflet coaptation loss. Preliminary feasibility assessment of two FMR treatments was performed in the developed model. Deer hearts showed ability to dilate under constant pressurization and have potential to be used for realistic preclinical research of novel FMR therapies. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12265-020-10071-y) contains supplementary material, which is available to authorized users. Springer US 2020-09-21 2021 /pmc/articles/PMC8219575/ /pubmed/32959169 http://dx.doi.org/10.1007/s12265-020-10071-y Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Jaworek, Michal
Mangini, Andrea
Maroncelli, Edoardo
Lucherini, Federico
Rosa, Rubina
Salurso, Eleonora
Votta, Emiliano
Antona, Carlo
Fiore, Gianfranco Beniamino
Vismara, Riccardo
Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title_full Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title_fullStr Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title_full_unstemmed Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title_short Ex Vivo Model of Functional Mitral Regurgitation Using Deer Hearts
title_sort ex vivo model of functional mitral regurgitation using deer hearts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219575/
https://www.ncbi.nlm.nih.gov/pubmed/32959169
http://dx.doi.org/10.1007/s12265-020-10071-y
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