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Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy
AIMS: Hypertrophic cardiomyopathy (HCM) is an important cause of heart failure-related disability over a wide range of ages. Profiles of severe progressive heart failure symptoms and death, or heart transplantation deserve more complete definition within large patient cohorts. METHODS AND RESULTS: C...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930982/ https://www.ncbi.nlm.nih.gov/pubmed/20513729 http://dx.doi.org/10.1093/eurheartj/ehq136 |
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author | Melacini, Paola Basso, Cristina Angelini, Annalisa Calore, Chiara Bobbo, Fabiana Tokajuk, Barbara Bellini, Nicoletta Smaniotto, Gessica Zucchetto, Mauro Iliceto, Sabino Thiene, Gaetano Maron, Barry J. |
author_facet | Melacini, Paola Basso, Cristina Angelini, Annalisa Calore, Chiara Bobbo, Fabiana Tokajuk, Barbara Bellini, Nicoletta Smaniotto, Gessica Zucchetto, Mauro Iliceto, Sabino Thiene, Gaetano Maron, Barry J. |
author_sort | Melacini, Paola |
collection | PubMed |
description | AIMS: Hypertrophic cardiomyopathy (HCM) is an important cause of heart failure-related disability over a wide range of ages. Profiles of severe progressive heart failure symptoms and death, or heart transplantation deserve more complete definition within large patient cohorts. METHODS AND RESULTS: Clinical and morphological features of heart failure were assessed in 293 consecutive HCM patients over a median follow-up of 6 (inter-quartile range 2–11) years. Gross and histopathological features were analysed in 12 patients for whom the heart was available for inspection. Of the 293 patients, 50 (17%) developed severe progressive heart failure, including 18 who died or were transplanted. Three profiles of heart failure were identified predominantly associated with: (i) end-stage systolic dysfunction (ejection fraction <50%) (15; 30%); (ii) left ventricular (LV) outflow obstruction at rest (11; 22%); and (iii) non-obstructive with preserved systolic function (24; 48%). Overall, atrial fibrillation (AF) contributed to heart failure in 32 patients (64%) among the three profiles. Compared with other patients, those non-obstructive with preserved systolic function had earlier onset of heart failure symptoms mainly due to diastolic dysfunction, and the most accelerated progression to advanced heart failure and adverse outcome (P = 0.04). Thrombi were identified in the left atrial appendage of five gross heart specimens all belonging to patients with AF, including three of which were unrecognized clinically and had previously embolized. Extensive myocardial scarring with LV remodelling was evident in all end-stage patients; no or only focal scars were present in other patients. CONCLUSION: Profiles of advanced heart failure in HCM are due to diverse pathophysiological mechanisms, including LV outflow obstruction and diastolic or global systolic ventricular dysfunction. Atrial fibrillation proved to be the most common disease variable associated with progressive heart failure. Recognition of the heterogeneous pathophysiology of heart failure in HCM is relevant, given the targeted management strategies necessary in this disease. |
format | Text |
id | pubmed-2930982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29309822010-09-02 Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy Melacini, Paola Basso, Cristina Angelini, Annalisa Calore, Chiara Bobbo, Fabiana Tokajuk, Barbara Bellini, Nicoletta Smaniotto, Gessica Zucchetto, Mauro Iliceto, Sabino Thiene, Gaetano Maron, Barry J. Eur Heart J Clinical Research AIMS: Hypertrophic cardiomyopathy (HCM) is an important cause of heart failure-related disability over a wide range of ages. Profiles of severe progressive heart failure symptoms and death, or heart transplantation deserve more complete definition within large patient cohorts. METHODS AND RESULTS: Clinical and morphological features of heart failure were assessed in 293 consecutive HCM patients over a median follow-up of 6 (inter-quartile range 2–11) years. Gross and histopathological features were analysed in 12 patients for whom the heart was available for inspection. Of the 293 patients, 50 (17%) developed severe progressive heart failure, including 18 who died or were transplanted. Three profiles of heart failure were identified predominantly associated with: (i) end-stage systolic dysfunction (ejection fraction <50%) (15; 30%); (ii) left ventricular (LV) outflow obstruction at rest (11; 22%); and (iii) non-obstructive with preserved systolic function (24; 48%). Overall, atrial fibrillation (AF) contributed to heart failure in 32 patients (64%) among the three profiles. Compared with other patients, those non-obstructive with preserved systolic function had earlier onset of heart failure symptoms mainly due to diastolic dysfunction, and the most accelerated progression to advanced heart failure and adverse outcome (P = 0.04). Thrombi were identified in the left atrial appendage of five gross heart specimens all belonging to patients with AF, including three of which were unrecognized clinically and had previously embolized. Extensive myocardial scarring with LV remodelling was evident in all end-stage patients; no or only focal scars were present in other patients. CONCLUSION: Profiles of advanced heart failure in HCM are due to diverse pathophysiological mechanisms, including LV outflow obstruction and diastolic or global systolic ventricular dysfunction. Atrial fibrillation proved to be the most common disease variable associated with progressive heart failure. Recognition of the heterogeneous pathophysiology of heart failure in HCM is relevant, given the targeted management strategies necessary in this disease. Oxford University Press 2010-09 2010-05-31 /pmc/articles/PMC2930982/ /pubmed/20513729 http://dx.doi.org/10.1093/eurheartj/ehq136 Text en Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2010. For permissions please email: journals.permissions@oxfordjournals.org http://creativecommons.org/licenses/by-nc/2.0/uk/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that the original authorship is properly and fully attributed; the Journal, Learned Society and Oxford University Press are attributed as the original place of publication with correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org. |
spellingShingle | Clinical Research Melacini, Paola Basso, Cristina Angelini, Annalisa Calore, Chiara Bobbo, Fabiana Tokajuk, Barbara Bellini, Nicoletta Smaniotto, Gessica Zucchetto, Mauro Iliceto, Sabino Thiene, Gaetano Maron, Barry J. Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title | Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title_full | Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title_fullStr | Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title_full_unstemmed | Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title_short | Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
title_sort | clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930982/ https://www.ncbi.nlm.nih.gov/pubmed/20513729 http://dx.doi.org/10.1093/eurheartj/ehq136 |
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