Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6363160 https://repositorio.unifesp.br/handle/11600/52132 |
Resumo: | Objectives: To evaluate the effects of antiplatelet and statin therapies on the interleukin profile in the acute phase of myocardial infarction and after 30 and 180 days. Methods: A prospective, randomized, open label trial with blinded endpoints aimed to compare four arms of therapies: Ticagrelor/Rosuvastatin (TR), Ticagrelor/Simvastatin (TS), Clopidogrel/Rosuvastatin (CR), Clopidogrel/Simvastatin (CS). The inflammatory response was assessed by IL1β, IL4, IL6, IL10, and IL18 concentrations by ELISA. One hundred and thirtyeight patients of both sexes with acute myocardial infarction with ST segment elevation (STEMI) were included and randomized to one of the four groups of treatment in the first 24hours. All patients followed a pharmacoinvasive strategy. Statistical analysis was performed to compare the effects between treatment groups at the baseline and after 30 and 180 days of the acute event. Results: The mean±SD age of the studied population was 56 ± 9 years, and 92 (66%) were male. The concentrations of IL1β, IL6 and IL18 did not show differences between groups of therapies at baseline. There was a decrease in the four arms of therapies for the concentrations of IL1β, IL6, and IL18 during the study followup. However, an increase in the concentrations of IL4 and IL10 was observed after 30 days of STEMI. There was no correlation at baseline, 30 days and 180 days between LDLC and CT levels and interleukins concentrations (except weak correlation with IL4 and IL6 at 180 days), suggesting low correlation between inflammation and lipids. Conclusions: All the strategies were equally associated with favorable changes in the interleukins profile throughout the treatment. |
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Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdioEffects of antiplatelets and statins on inflammatory biomarkers after acute myocardial infarctionInflammationInterleukinsAntiplateletsStatinsAcute myocardial infarctionInflamaçãoInterleucinasAntiplaquetáriosEstatinasInfarto agudo do miocárdioObjectives: To evaluate the effects of antiplatelet and statin therapies on the interleukin profile in the acute phase of myocardial infarction and after 30 and 180 days. Methods: A prospective, randomized, open label trial with blinded endpoints aimed to compare four arms of therapies: Ticagrelor/Rosuvastatin (TR), Ticagrelor/Simvastatin (TS), Clopidogrel/Rosuvastatin (CR), Clopidogrel/Simvastatin (CS). The inflammatory response was assessed by IL1β, IL4, IL6, IL10, and IL18 concentrations by ELISA. One hundred and thirtyeight patients of both sexes with acute myocardial infarction with ST segment elevation (STEMI) were included and randomized to one of the four groups of treatment in the first 24hours. All patients followed a pharmacoinvasive strategy. Statistical analysis was performed to compare the effects between treatment groups at the baseline and after 30 and 180 days of the acute event. Results: The mean±SD age of the studied population was 56 ± 9 years, and 92 (66%) were male. The concentrations of IL1β, IL6 and IL18 did not show differences between groups of therapies at baseline. There was a decrease in the four arms of therapies for the concentrations of IL1β, IL6, and IL18 during the study followup. However, an increase in the concentrations of IL4 and IL10 was observed after 30 days of STEMI. There was no correlation at baseline, 30 days and 180 days between LDLC and CT levels and interleukins concentrations (except weak correlation with IL4 and IL6 at 180 days), suggesting low correlation between inflammation and lipids. Conclusions: All the strategies were equally associated with favorable changes in the interleukins profile throughout the treatment.Objetivos: Avaliar os efeitos da terapia baseada em antiplaquetários e estatinas sobre o perfil de interleucinas após o infarto agudo do miocárdio na fase aguda e após 30 e 180 dias. Métodos: Estudo prospectivo, aberto, aleatório e com análise cega de desfechos com quatro braços de terapias: Ticagrelor/Rosuvastatina (TR), Ticagrelor/Sinvastatina (TS),Clopidogrel/Rosuvastatina (CR),Clopidogrel/Sinvastatina (CS). Foi avaliada a resposta inflamatória or meio das concentrações das interleucinas IL1β, IL4, IL6, IL10 e IL18, pela técnica de ELISA. Foram incluídos 138 pacientes de ambos os sexos, na fase aguda do infarto do miocárdio com supradesnível do segmento ST sob estratégia farmacoinvasiva. A análise estatística examinou efeitos entre grupos de tratamento no período basal e durante o seguimento aos 30 e 180 dias após o infarto. Resultados: A idade média ±DP da população estudada foi de 56±9 anos, sendo 92 (66%) do sexo masculino. As concentrações de IL1β, IL6 e IL18 não apresentaram diferenças entre os grupos de terapias no período basal. Os quatro braços de terapias foram associados com reduções nas concentrações de IL1β, IL6 e IL18 durante o seguimento do estudo. Contudo, para IL4 e IL10 foi observado aumento dos níveis após 30 dias do infarto. Não houve correlação na condição basal, 30 dias e 180 dias entre níveis de LDL ou CT com relação às concentrações das interleucinas (exceto fraca correlação de IL4 e IL6 aos 180 dias), sugerindo que a inflamação tem baixa correlação com a hipercolesterolemia. Conclusões: As estratégias terapêuticas instituídas se associaram de forma similar com modificações favoráveis no perfil das interleucinas analisadas ao longo do estudo.Dados abertos - Sucupira - Teses e dissertações (2018)Fundação de Amparo à Pesquisa do Estado de São Paulo (Fapesp),Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Federal de São Paulo (UNIFESP)Fonseca, Francisco Antonio Helfenstein [UNIFESP]http://lattes.cnpq.br/2393476657163442http://lattes.cnpq.br/9175147931402957Universidade Federal de São Paulo (UNIFESP)Coste, Maria Esther Rochael [UNIFESP]2020-03-25T11:43:22Z2020-03-25T11:43:22Z2018-08-30info:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion87 f.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=63631602018-0045.pdfhttps://repositorio.unifesp.br/handle/11600/52132porSão Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-02T12:16:26Zoai:repositorio.unifesp.br/:11600/52132Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-02T12:16:26Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio Effects of antiplatelets and statins on inflammatory biomarkers after acute myocardial infarction |
title |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
spellingShingle |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio Coste, Maria Esther Rochael [UNIFESP] Inflammation Interleukins Antiplatelets Statins Acute myocardial infarction Inflamação Interleucinas Antiplaquetários Estatinas Infarto agudo do miocárdio |
title_short |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
title_full |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
title_fullStr |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
title_full_unstemmed |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
title_sort |
Efeitos de antiplaquetários e estatinas em marcadores inflamatórios após infarto agudo do miocárdio |
author |
Coste, Maria Esther Rochael [UNIFESP] |
author_facet |
Coste, Maria Esther Rochael [UNIFESP] |
author_role |
author |
dc.contributor.none.fl_str_mv |
Fonseca, Francisco Antonio Helfenstein [UNIFESP] http://lattes.cnpq.br/2393476657163442 http://lattes.cnpq.br/9175147931402957 Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Coste, Maria Esther Rochael [UNIFESP] |
dc.subject.por.fl_str_mv |
Inflammation Interleukins Antiplatelets Statins Acute myocardial infarction Inflamação Interleucinas Antiplaquetários Estatinas Infarto agudo do miocárdio |
topic |
Inflammation Interleukins Antiplatelets Statins Acute myocardial infarction Inflamação Interleucinas Antiplaquetários Estatinas Infarto agudo do miocárdio |
description |
Objectives: To evaluate the effects of antiplatelet and statin therapies on the interleukin profile in the acute phase of myocardial infarction and after 30 and 180 days. Methods: A prospective, randomized, open label trial with blinded endpoints aimed to compare four arms of therapies: Ticagrelor/Rosuvastatin (TR), Ticagrelor/Simvastatin (TS), Clopidogrel/Rosuvastatin (CR), Clopidogrel/Simvastatin (CS). The inflammatory response was assessed by IL1β, IL4, IL6, IL10, and IL18 concentrations by ELISA. One hundred and thirtyeight patients of both sexes with acute myocardial infarction with ST segment elevation (STEMI) were included and randomized to one of the four groups of treatment in the first 24hours. All patients followed a pharmacoinvasive strategy. Statistical analysis was performed to compare the effects between treatment groups at the baseline and after 30 and 180 days of the acute event. Results: The mean±SD age of the studied population was 56 ± 9 years, and 92 (66%) were male. The concentrations of IL1β, IL6 and IL18 did not show differences between groups of therapies at baseline. There was a decrease in the four arms of therapies for the concentrations of IL1β, IL6, and IL18 during the study followup. However, an increase in the concentrations of IL4 and IL10 was observed after 30 days of STEMI. There was no correlation at baseline, 30 days and 180 days between LDLC and CT levels and interleukins concentrations (except weak correlation with IL4 and IL6 at 180 days), suggesting low correlation between inflammation and lipids. Conclusions: All the strategies were equally associated with favorable changes in the interleukins profile throughout the treatment. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-08-30 2020-03-25T11:43:22Z 2020-03-25T11:43:22Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6363160 2018-0045.pdf https://repositorio.unifesp.br/handle/11600/52132 |
url |
https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6363160 https://repositorio.unifesp.br/handle/11600/52132 |
identifier_str_mv |
2018-0045.pdf |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
87 f. application/pdf |
dc.coverage.none.fl_str_mv |
São Paulo |
dc.publisher.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
publisher.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268384697647104 |