The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/45873 |
Resumo: | OBJECTIVE: Chagas' disease has spread throughout Latin America because of the high rate of migration among these countries. Approximately 30% of Chagas' patients will develop cardiomyopathy, and 10% of these will develop severe cardiac damage leading to heart failure. Beta-blockade improves symptoms and survival in heart failure patients; however, its efficacy has not been well established in Chagas' disease. We evaluated the role of carvedilol in cardiac remodeling and mortality in a Chagas' cardiomyopathy animal model. METHODS: We studied Trypanosoma cruzi infection in 55 Syrian hamsters that were divided into three groups: control (15), infected (20), and infected + carvedilol (20). Animals underwent echocardiography, electrocardiography, and morphometry for collagen evaluation in ventricles stained with picrosirius red. RESULTS: The left ventricular diastolic diameter did not change between groups, although it was slightly larger in infected groups, as was left ventricular systolic diameter. Fractional shortening also did not change between groups, although it was slightly lower in infected groups. Collagen accumulation in the interstitial myocardial space was significantly higher in infected groups and was not attenuated by carvedilol. The same response was observed in the perivascular space. The survival curve showed significantly better survival in the control group compared with the infected groups; but no benefit of carvedilol was observed during the study. However, in the acute phase (up to 100 days of infection), carvedilol did reduce mortality. CONCLUSION: Carvedilol did not attenuate cardiac remodeling or mortality in this model of Chagas' cardiomyopathy. The treatment did improve survival in the acute phase of the disease. |
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Clinics |
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The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathyChagas' CardiomyopathyMyocardial FibrosisBeta-BlockerCardiac DysfunctionMyocardial RemodelingOBJECTIVE: Chagas' disease has spread throughout Latin America because of the high rate of migration among these countries. Approximately 30% of Chagas' patients will develop cardiomyopathy, and 10% of these will develop severe cardiac damage leading to heart failure. Beta-blockade improves symptoms and survival in heart failure patients; however, its efficacy has not been well established in Chagas' disease. We evaluated the role of carvedilol in cardiac remodeling and mortality in a Chagas' cardiomyopathy animal model. METHODS: We studied Trypanosoma cruzi infection in 55 Syrian hamsters that were divided into three groups: control (15), infected (20), and infected + carvedilol (20). Animals underwent echocardiography, electrocardiography, and morphometry for collagen evaluation in ventricles stained with picrosirius red. RESULTS: The left ventricular diastolic diameter did not change between groups, although it was slightly larger in infected groups, as was left ventricular systolic diameter. Fractional shortening also did not change between groups, although it was slightly lower in infected groups. Collagen accumulation in the interstitial myocardial space was significantly higher in infected groups and was not attenuated by carvedilol. The same response was observed in the perivascular space. The survival curve showed significantly better survival in the control group compared with the infected groups; but no benefit of carvedilol was observed during the study. However, in the acute phase (up to 100 days of infection), carvedilol did reduce mortality. CONCLUSION: Carvedilol did not attenuate cardiac remodeling or mortality in this model of Chagas' cardiomyopathy. The treatment did improve survival in the acute phase of the disease.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/4587310.6061/clinics/2012(09)14Clinics; Vol. 67 No. 9 (2012); 1063-1069Clinics; v. 67 n. 9 (2012); 1063-1069Clinics; Vol. 67 Núm. 9 (2012); 1063-10691980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/45873/49476Pimentel, Walace de SouzaRamires, Felix José Alvarezlanni, Barbara MariaSalemi, Vera Maria CuryBilate, Angelina Morand BianchiCunha-Neto, EdecioOliveira, Adriana Morgan deFernandes, FábioMady, Charlesinfo:eu-repo/semantics/openAccess2012-10-10T20:42:29Zoai:revistas.usp.br:article/45873Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-10-10T20:42:29Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
title |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
spellingShingle |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy Pimentel, Walace de Souza Chagas' Cardiomyopathy Myocardial Fibrosis Beta-Blocker Cardiac Dysfunction Myocardial Remodeling |
title_short |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
title_full |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
title_fullStr |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
title_full_unstemmed |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
title_sort |
The effect of beta-blockade on myocardial remodelling in Chagas' cardiomyopathy |
author |
Pimentel, Walace de Souza |
author_facet |
Pimentel, Walace de Souza Ramires, Felix José Alvarez lanni, Barbara Maria Salemi, Vera Maria Cury Bilate, Angelina Morand Bianchi Cunha-Neto, Edecio Oliveira, Adriana Morgan de Fernandes, Fábio Mady, Charles |
author_role |
author |
author2 |
Ramires, Felix José Alvarez lanni, Barbara Maria Salemi, Vera Maria Cury Bilate, Angelina Morand Bianchi Cunha-Neto, Edecio Oliveira, Adriana Morgan de Fernandes, Fábio Mady, Charles |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Pimentel, Walace de Souza Ramires, Felix José Alvarez lanni, Barbara Maria Salemi, Vera Maria Cury Bilate, Angelina Morand Bianchi Cunha-Neto, Edecio Oliveira, Adriana Morgan de Fernandes, Fábio Mady, Charles |
dc.subject.por.fl_str_mv |
Chagas' Cardiomyopathy Myocardial Fibrosis Beta-Blocker Cardiac Dysfunction Myocardial Remodeling |
topic |
Chagas' Cardiomyopathy Myocardial Fibrosis Beta-Blocker Cardiac Dysfunction Myocardial Remodeling |
description |
OBJECTIVE: Chagas' disease has spread throughout Latin America because of the high rate of migration among these countries. Approximately 30% of Chagas' patients will develop cardiomyopathy, and 10% of these will develop severe cardiac damage leading to heart failure. Beta-blockade improves symptoms and survival in heart failure patients; however, its efficacy has not been well established in Chagas' disease. We evaluated the role of carvedilol in cardiac remodeling and mortality in a Chagas' cardiomyopathy animal model. METHODS: We studied Trypanosoma cruzi infection in 55 Syrian hamsters that were divided into three groups: control (15), infected (20), and infected + carvedilol (20). Animals underwent echocardiography, electrocardiography, and morphometry for collagen evaluation in ventricles stained with picrosirius red. RESULTS: The left ventricular diastolic diameter did not change between groups, although it was slightly larger in infected groups, as was left ventricular systolic diameter. Fractional shortening also did not change between groups, although it was slightly lower in infected groups. Collagen accumulation in the interstitial myocardial space was significantly higher in infected groups and was not attenuated by carvedilol. The same response was observed in the perivascular space. The survival curve showed significantly better survival in the control group compared with the infected groups; but no benefit of carvedilol was observed during the study. However, in the acute phase (up to 100 days of infection), carvedilol did reduce mortality. CONCLUSION: Carvedilol did not attenuate cardiac remodeling or mortality in this model of Chagas' cardiomyopathy. The treatment did improve survival in the acute phase of the disease. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-09-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/45873 10.6061/clinics/2012(09)14 |
url |
https://www.revistas.usp.br/clinics/article/view/45873 |
identifier_str_mv |
10.6061/clinics/2012(09)14 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/45873/49476 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 67 No. 9 (2012); 1063-1069 Clinics; v. 67 n. 9 (2012); 1063-1069 Clinics; Vol. 67 Núm. 9 (2012); 1063-1069 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222759139147776 |