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Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease

INTRODUCTION: Mitral valve (MV) prolapse (MVP) is a primary valvular abnormality. We hypothesized that additionally there are concomitant abnormalities of the left ventricle (LV) and MV apparatus in this entity even in the absence of significant mitral regurgitation (MR). OBJECTIVE: To characterize...

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Autores principales: Romero Daza, Angélica, Chokshi, Aalap, Pardo, Patricia, Maneiro, Nicolas, Guijarro Contreras, Ana, Larrañaga-Moreira, Jose M., Ibañez, Borja, Fuster, Valentin, Fernández Friera, Leticia, Solís, Jorge, Sanz, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504058/
https://www.ncbi.nlm.nih.gov/pubmed/34629093
http://dx.doi.org/10.1186/s12968-021-00800-w
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author Romero Daza, Angélica
Chokshi, Aalap
Pardo, Patricia
Maneiro, Nicolas
Guijarro Contreras, Ana
Larrañaga-Moreira, Jose M.
Ibañez, Borja
Fuster, Valentin
Fernández Friera, Leticia
Solís, Jorge
Sanz, Javier
author_facet Romero Daza, Angélica
Chokshi, Aalap
Pardo, Patricia
Maneiro, Nicolas
Guijarro Contreras, Ana
Larrañaga-Moreira, Jose M.
Ibañez, Borja
Fuster, Valentin
Fernández Friera, Leticia
Solís, Jorge
Sanz, Javier
author_sort Romero Daza, Angélica
collection PubMed
description INTRODUCTION: Mitral valve (MV) prolapse (MVP) is a primary valvular abnormality. We hypothesized that additionally there are concomitant abnormalities of the left ventricle (LV) and MV apparatus in this entity even in the absence of significant mitral regurgitation (MR). OBJECTIVE: To characterize MV and LV anatomic and functional features in MVP with preserved LV ejection fraction, with and without significant MR, using cardiovascular magnetic resonance (CMR). METHODS: Consecutive MVP patients (n = 80, mean 52 years, 37% males) with preserved LV ejection fraction, and 44 controls (46 years, 52% males) by CMR were included, as well as 13 additional patients with “borderline” MVP. From cine images we quantified LV volumes, MV and LV anatomic measurements (including angle between diastolic and systolic annular planes, annular displacement, and basal inferolateral hypertrophy) and, using feature tracking, longitudinal and circumferential peak systolic strains. RESULTS: Significant MR was found in 46 (56%) MVP patients. Compared with controls, MVP patients had LV enlargement, basal inferolateral hypertrophy, higher posterior annular excursion, and reduced shortening of the papillary muscles. LV basal strains were significantly increased, particularly in several basal segments. These differences remained significant in patients without significant MR, and many persisted in “borderline” MVP. CONCLUSIONS: In patients with MVP and preserved LV ejection fraction there is LV dilatation, basal inferolateral hypertrophy, exaggerated posterior annular displacement and increased basal deformation, even in the absence of significant MR or overt MVP. These findings suggest that MVP is a disease not only of the MV but also of the adjacent myocardium. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-021-00800-w.
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spelling pubmed-85040582021-10-25 Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease Romero Daza, Angélica Chokshi, Aalap Pardo, Patricia Maneiro, Nicolas Guijarro Contreras, Ana Larrañaga-Moreira, Jose M. Ibañez, Borja Fuster, Valentin Fernández Friera, Leticia Solís, Jorge Sanz, Javier J Cardiovasc Magn Reson Research INTRODUCTION: Mitral valve (MV) prolapse (MVP) is a primary valvular abnormality. We hypothesized that additionally there are concomitant abnormalities of the left ventricle (LV) and MV apparatus in this entity even in the absence of significant mitral regurgitation (MR). OBJECTIVE: To characterize MV and LV anatomic and functional features in MVP with preserved LV ejection fraction, with and without significant MR, using cardiovascular magnetic resonance (CMR). METHODS: Consecutive MVP patients (n = 80, mean 52 years, 37% males) with preserved LV ejection fraction, and 44 controls (46 years, 52% males) by CMR were included, as well as 13 additional patients with “borderline” MVP. From cine images we quantified LV volumes, MV and LV anatomic measurements (including angle between diastolic and systolic annular planes, annular displacement, and basal inferolateral hypertrophy) and, using feature tracking, longitudinal and circumferential peak systolic strains. RESULTS: Significant MR was found in 46 (56%) MVP patients. Compared with controls, MVP patients had LV enlargement, basal inferolateral hypertrophy, higher posterior annular excursion, and reduced shortening of the papillary muscles. LV basal strains were significantly increased, particularly in several basal segments. These differences remained significant in patients without significant MR, and many persisted in “borderline” MVP. CONCLUSIONS: In patients with MVP and preserved LV ejection fraction there is LV dilatation, basal inferolateral hypertrophy, exaggerated posterior annular displacement and increased basal deformation, even in the absence of significant MR or overt MVP. These findings suggest that MVP is a disease not only of the MV but also of the adjacent myocardium. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-021-00800-w. BioMed Central 2021-10-11 /pmc/articles/PMC8504058/ /pubmed/34629093 http://dx.doi.org/10.1186/s12968-021-00800-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Romero Daza, Angélica
Chokshi, Aalap
Pardo, Patricia
Maneiro, Nicolas
Guijarro Contreras, Ana
Larrañaga-Moreira, Jose M.
Ibañez, Borja
Fuster, Valentin
Fernández Friera, Leticia
Solís, Jorge
Sanz, Javier
Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title_full Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title_fullStr Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title_full_unstemmed Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title_short Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
title_sort mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504058/
https://www.ncbi.nlm.nih.gov/pubmed/34629093
http://dx.doi.org/10.1186/s12968-021-00800-w
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