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Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse
OBJECTIVES: We aimed to evaluate the relationship between mitral annular disjunction (MAD) severity and myocardial interstitial fibrosis at the left ventricular (LV) base in patients with mitral valve prolapse (MVP), and to assess the association between severity of interstitial fibrosis and the occ...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438990/ https://www.ncbi.nlm.nih.gov/pubmed/34517908 http://dx.doi.org/10.1186/s12968-021-00797-2 |
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author | Pavon, Anna Giulia Arangalage, Dimitri Pascale, Patrizio Hugelshofer, Sarah Rutz, Tobias Porretta, Alessandra Pia Le Bloa, Mathieu Muller, Olivier Pruvot, Etienne Schwitter, Juerg Monney, Pierre |
author_facet | Pavon, Anna Giulia Arangalage, Dimitri Pascale, Patrizio Hugelshofer, Sarah Rutz, Tobias Porretta, Alessandra Pia Le Bloa, Mathieu Muller, Olivier Pruvot, Etienne Schwitter, Juerg Monney, Pierre |
author_sort | Pavon, Anna Giulia |
collection | PubMed |
description | OBJECTIVES: We aimed to evaluate the relationship between mitral annular disjunction (MAD) severity and myocardial interstitial fibrosis at the left ventricular (LV) base in patients with mitral valve prolapse (MVP), and to assess the association between severity of interstitial fibrosis and the occurrence of ventricular arrhythmic events. BACKGROUND: In MVP, MAD has been associated with myocardial replacement fibrosis and arrhythmia, but the importance of interstitial fibrosis remains unknown. METHODS: In this retrospective study, 30 patients with MVP and MAD (MVP–MAD) underwent cardiovascular magnetic resonance (CMR) with assessment of MAD length, late gadolinium enhancement (LGE), and basal segments myocardial extracellular volume (ECVsyn). The control group included 14 patients with mitral regurgitation (MR) but no MAD (MR-NoMAD) and 10 patients with normal CMR (NoMR-NoMAD). Fifteen MVP–MAD patients underwent 24 h-Holter monitoring. RESULTS: LGE was observed in 47% of MVP–MAD patients and was absent in all controls. ECVsyn was higher in MVP–MAD (30 ± 3% vs 24 ± 3% MR-NoMAD, p < 0.001 and vs 24 ± 2% NoMR-NoMAD, p < 0.001), even in MVP–MAD patients without LGE (29 ± 3% vs 24 ± 3%, p < 0.001 and vs 24 ± 2%, p < 0.001, respectively). MAD length correlated with ECVsyn (rho = 0.61, p < 0.001), but not with LGE extent. Four patients had history of out-of-hospital cardiac arrest; LGE and ECVsyn were equally performant to identify those high-risk patients, area under the receiver operating characteristic (ROC) curve 0.81 vs 0.83, p = 0.84). Among patients with Holter, 87% had complex ventricular arrhythmia. ECVsyn was above the cut-off value in all while only 53% had LGE. CONCLUSION: Increase in ECVsyn, a marker of interstitial fibrosis, occurs in MVP–MAD even in the absence of LGE, and was correlated with MAD length and increased risk of out-of-hospital cardiac arrest. ECV should be includedin the CMR examination of MVP patients in an effort to better assess fibrous remodelling as it may provide additional value beyond the assessment of LGE in the arrhythmic risk stratification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-021-00797-2. |
format | Online Article Text |
id | pubmed-8438990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84389902021-09-14 Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse Pavon, Anna Giulia Arangalage, Dimitri Pascale, Patrizio Hugelshofer, Sarah Rutz, Tobias Porretta, Alessandra Pia Le Bloa, Mathieu Muller, Olivier Pruvot, Etienne Schwitter, Juerg Monney, Pierre J Cardiovasc Magn Reson Research OBJECTIVES: We aimed to evaluate the relationship between mitral annular disjunction (MAD) severity and myocardial interstitial fibrosis at the left ventricular (LV) base in patients with mitral valve prolapse (MVP), and to assess the association between severity of interstitial fibrosis and the occurrence of ventricular arrhythmic events. BACKGROUND: In MVP, MAD has been associated with myocardial replacement fibrosis and arrhythmia, but the importance of interstitial fibrosis remains unknown. METHODS: In this retrospective study, 30 patients with MVP and MAD (MVP–MAD) underwent cardiovascular magnetic resonance (CMR) with assessment of MAD length, late gadolinium enhancement (LGE), and basal segments myocardial extracellular volume (ECVsyn). The control group included 14 patients with mitral regurgitation (MR) but no MAD (MR-NoMAD) and 10 patients with normal CMR (NoMR-NoMAD). Fifteen MVP–MAD patients underwent 24 h-Holter monitoring. RESULTS: LGE was observed in 47% of MVP–MAD patients and was absent in all controls. ECVsyn was higher in MVP–MAD (30 ± 3% vs 24 ± 3% MR-NoMAD, p < 0.001 and vs 24 ± 2% NoMR-NoMAD, p < 0.001), even in MVP–MAD patients without LGE (29 ± 3% vs 24 ± 3%, p < 0.001 and vs 24 ± 2%, p < 0.001, respectively). MAD length correlated with ECVsyn (rho = 0.61, p < 0.001), but not with LGE extent. Four patients had history of out-of-hospital cardiac arrest; LGE and ECVsyn were equally performant to identify those high-risk patients, area under the receiver operating characteristic (ROC) curve 0.81 vs 0.83, p = 0.84). Among patients with Holter, 87% had complex ventricular arrhythmia. ECVsyn was above the cut-off value in all while only 53% had LGE. CONCLUSION: Increase in ECVsyn, a marker of interstitial fibrosis, occurs in MVP–MAD even in the absence of LGE, and was correlated with MAD length and increased risk of out-of-hospital cardiac arrest. ECV should be includedin the CMR examination of MVP patients in an effort to better assess fibrous remodelling as it may provide additional value beyond the assessment of LGE in the arrhythmic risk stratification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-021-00797-2. BioMed Central 2021-09-13 /pmc/articles/PMC8438990/ /pubmed/34517908 http://dx.doi.org/10.1186/s12968-021-00797-2 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 Pavon, Anna Giulia Arangalage, Dimitri Pascale, Patrizio Hugelshofer, Sarah Rutz, Tobias Porretta, Alessandra Pia Le Bloa, Mathieu Muller, Olivier Pruvot, Etienne Schwitter, Juerg Monney, Pierre Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title | Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title_full | Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title_fullStr | Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title_full_unstemmed | Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title_short | Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse |
title_sort | myocardial extracellular volume by t1 mapping: a new marker of arrhythmia in mitral valve prolapse |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438990/ https://www.ncbi.nlm.nih.gov/pubmed/34517908 http://dx.doi.org/10.1186/s12968-021-00797-2 |
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