Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica

Detalhes bibliográficos
Autor(a) principal: Monteiro, Carlos Manoel de Castro [UNIFESP]
Data de Publicação: 2009
Outros Autores: Oliveira, Luciene [UNIFESP], Izar, Maria Cristina de Oliveira [UNIFESP], Helfenstein, Tatiana [UNIFESP], Santos, Andreza Oliveira dos [UNIFESP], Fischer, Simone M. [UNIFESP], Barros, Sahana W. [UNIFESP], Pinheiro, Luiz Fernando Muniz [UNIFESP], Carvalho, Antonio Carlos [UNIFESP], Fonseca, Francisco Antonio Helfenstein [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0066-782X2009000200004
http://repositorio.unifesp.br/handle/11600/4890
Resumo: BACKGROUND: Patients with metabolic syndrome (MetS) are at high coronary risk and beta-cell dysfunction or insulin resistance might predict an additional risk for early cardiovascular events. OBJECTIVE: This study aimed to evaluate early glucometabolic alterations in patients with MetS, but without previously known type 2 diabetes, after acute coronary syndrome. METHODS: A total of 114 patients were submitted to an oral glucose tolerance test (OGTT) 1-3 days after hospital discharge due to myocardial infarction or unstable angina. Based on the OGTT, we defined three groups of patients: normal glucose tolerance (NGT; n=26), impaired glucose tolerance (IGT; n=39), or diabetes (DM; n=49). The homeostasis model assessment (HOMA-IR) was used to measure insulin resistance; beta-cell responsiveness was assessed by the insulinogenic index at 30 min (ΔI30/ΔG30). RESULTS: Based on the HOMA-IR, patients with DM were more insulin-resistant than those with NGT or IGT (p<0.001). According to the insulinogenic index, the beta-cell responsiveness was also impaired in subjects with DM (p<0.001 vs NGT or IGT). CONCLUSION: High rates of glucometabolic alterations were found after acute coronary syndrome in patients with MetS. As these abnormalities markedly increase the risk for adverse outcomes, early OGTT among MetS patients might be used to identify those at the highest coronary risk.
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spelling Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólicaEarly glucometabolic profile in patients with acute coronary syndromes and metabolic syndromePerfil glucometabólico inicial en pacientes con síndrome coronario agudo y síndrome metabólicoInsulin resistancemetabolic syndromeacute coronary syndromediabetes mellitus, type 2insulin-secreting cellsResistência à insulinasíndrome metabólicasíndrome coronariana agudadiabetes mellitus tipo 2células secretoras de insulinaBACKGROUND: Patients with metabolic syndrome (MetS) are at high coronary risk and beta-cell dysfunction or insulin resistance might predict an additional risk for early cardiovascular events. OBJECTIVE: This study aimed to evaluate early glucometabolic alterations in patients with MetS, but without previously known type 2 diabetes, after acute coronary syndrome. METHODS: A total of 114 patients were submitted to an oral glucose tolerance test (OGTT) 1-3 days after hospital discharge due to myocardial infarction or unstable angina. Based on the OGTT, we defined three groups of patients: normal glucose tolerance (NGT; n=26), impaired glucose tolerance (IGT; n=39), or diabetes (DM; n=49). The homeostasis model assessment (HOMA-IR) was used to measure insulin resistance; beta-cell responsiveness was assessed by the insulinogenic index at 30 min (ΔI30/ΔG30). RESULTS: Based on the HOMA-IR, patients with DM were more insulin-resistant than those with NGT or IGT (p<0.001). According to the insulinogenic index, the beta-cell responsiveness was also impaired in subjects with DM (p<0.001 vs NGT or IGT). CONCLUSION: High rates of glucometabolic alterations were found after acute coronary syndrome in patients with MetS. As these abnormalities markedly increase the risk for adverse outcomes, early OGTT among MetS patients might be used to identify those at the highest coronary risk.FUNDAMENTO: Pacientes con síndrome metabólico (SM) tienen alto riesgo coronario y la disfunción de la célula beta o la resistencia a la insulina puede prever un riesgo adicional de eventos cardiovasculares precoces. OBJETIVO: Evaluar las alteraciones glucometabólicas precoces en pacientes con SM, pero sin diagnóstico de diabetes tipo 2, tras el síndrome coronario agudo. MÉTODOS: Un total de 114 pacientes fue sometido a la prueba oral de tolerancia a la glucosa (POTG), de un a tres días tras el alta hospitalaria, y luego de infarto agudo de miocardio o angina inestable. Basado en el POTG, definimos tres grupos de pacientes: tolerancia normal a la glucosa (TNG; n=26), tolerancia alterada a la glucosa (TAG; n=39) o diabetes mellitus (DM; n=49). Se utilizó el Modelo de Evaluación de la Homeostasis (HOMA-IR) para estimarse la resistencia a la insulina; se evaluó la responsividad de la célula beta a través del índice insulinogénico de 30 minutos (ΔI30/ΔG30). RESULTADOS: Basado en el HOMA-IR, los pacientes con DM se mostraban más insulinoresistentes que los individuos con TNG o TAG (p<0,001). De acuerdo con el índice insulinogénico, la responsividad de la célula beta también estaba alterada en individuos con DM (p<0,001 vs. TNG o TAG). CONCLUSIONES: Se encontraron altas tasas de alteraciones glucometabólicas tras el síndrome coronario agudo en pacientes con SM. Como esas anormalidades incrementan acentuadamente el riesgo de desenlaces adversos, el POTG precoz se puede utilizar en pacientes con SM para identificar a los que presentan mayor riesgo coronario.FUNDAMENTO: Pacientes com síndrome metabólica (SM) têm alto risco coronariano e a disfunção da célula beta ou resistência à insulina pode prever um risco adicional de eventos cardiovasculares precoces. OBJETIVO: Avaliar as alterações glicometabólicas precoces em pacientes com SM, mas sem diagnóstico de diabete tipo 2, após síndrome coronariana aguda. MÉTODOS: Um total de 114 pacientes foi submetido ao teste oral de tolerância à glicose (TOTG), 1-3 dias da alta hospitalar, após infarto agudo do miocárdio ou angina instável. Baseado no TOTG, definimos três grupos de pacientes: tolerância normal à glicose (TNG; n=26), tolerância alterada à glicose (TAG; n=39) ou diabetes mellitus (DM; n=49). O Modelo de Avaliação da Homeostase (HOMA-IR) foi usado para estimar a resistência à insulina; a responsividade da célula beta foi avaliada através do índice insulinogênico de 30 minutos (ΔI30/ΔG30). RESULTADOS: Baseado no HOMA-IR, os pacientes com DM eram mais insulino-resistentes do que aqueles com TNG ou TAG (p<0,001). De acordo com o índice insulinogênico, a responsividade da célula beta também estava alterada em indivíduos com DM (p<0,001 vs TNG ou TAG). CONCLUSÃO: Altas taxas de alterações glicometabólicas foram encontradas após síndrome coronariana aguda em pacientes com SM. Como essas anormalidades acentuadamente aumentam o risco de desfechos adversos, o TOTG precoce pode ser utilizado em pacientes com SM para identificar aqueles que apresentam maior risco coronariano.Universidade Federal de São Paulo (UNIFESP)UNIFESP, EPM, Sao Paulo, BrazilSciELOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Sociedade Brasileira de Cardiologia - SBCUniversidade Federal de São Paulo (UNIFESP)Monteiro, Carlos Manoel de Castro [UNIFESP]Oliveira, Luciene [UNIFESP]Izar, Maria Cristina de Oliveira [UNIFESP]Helfenstein, Tatiana [UNIFESP]Santos, Andreza Oliveira dos [UNIFESP]Fischer, Simone M. [UNIFESP]Barros, Sahana W. [UNIFESP]Pinheiro, Luiz Fernando Muniz [UNIFESP]Carvalho, Antonio Carlos [UNIFESP]Fonseca, Francisco Antonio Helfenstein [UNIFESP]2015-06-14T13:39:04Z2015-06-14T13:39:04Z2009-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion94-99application/pdfapplication/pdfapplication/pdfhttp://dx.doi.org/10.1590/S0066-782X2009000200004Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 92, n. 2, p. 94-99, 2009.10.1590/S0066-782X2009000200004S0066-782X2009000200004-en.pdfS0066-782X2009000200004-es.pdfS0066-782X2009000200004-pt.pdf0066-782XS0066-782X2009000200004http://repositorio.unifesp.br/handle/11600/4890WOS:000265050600004porArquivos Brasileiros de Cardiologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-10-14T13:57:40Zoai:repositorio.unifesp.br/:11600/4890Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-10-14T13:57:40Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
Early glucometabolic profile in patients with acute coronary syndromes and metabolic syndrome
Perfil glucometabólico inicial en pacientes con síndrome coronario agudo y síndrome metabólico
title Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
spellingShingle Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
Monteiro, Carlos Manoel de Castro [UNIFESP]
Insulin resistance
metabolic syndrome
acute coronary syndrome
diabetes mellitus, type 2
insulin-secreting cells
Resistência à insulina
síndrome metabólica
síndrome coronariana aguda
diabetes mellitus tipo 2
células secretoras de insulina
title_short Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
title_full Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
title_fullStr Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
title_full_unstemmed Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
title_sort Perfil glicometabólico inicial em pacientes com síndrome coronariana aguda e síndrome metabólica
author Monteiro, Carlos Manoel de Castro [UNIFESP]
author_facet Monteiro, Carlos Manoel de Castro [UNIFESP]
Oliveira, Luciene [UNIFESP]
Izar, Maria Cristina de Oliveira [UNIFESP]
Helfenstein, Tatiana [UNIFESP]
Santos, Andreza Oliveira dos [UNIFESP]
Fischer, Simone M. [UNIFESP]
Barros, Sahana W. [UNIFESP]
Pinheiro, Luiz Fernando Muniz [UNIFESP]
Carvalho, Antonio Carlos [UNIFESP]
Fonseca, Francisco Antonio Helfenstein [UNIFESP]
author_role author
author2 Oliveira, Luciene [UNIFESP]
Izar, Maria Cristina de Oliveira [UNIFESP]
Helfenstein, Tatiana [UNIFESP]
Santos, Andreza Oliveira dos [UNIFESP]
Fischer, Simone M. [UNIFESP]
Barros, Sahana W. [UNIFESP]
Pinheiro, Luiz Fernando Muniz [UNIFESP]
Carvalho, Antonio Carlos [UNIFESP]
Fonseca, Francisco Antonio Helfenstein [UNIFESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Monteiro, Carlos Manoel de Castro [UNIFESP]
Oliveira, Luciene [UNIFESP]
Izar, Maria Cristina de Oliveira [UNIFESP]
Helfenstein, Tatiana [UNIFESP]
Santos, Andreza Oliveira dos [UNIFESP]
Fischer, Simone M. [UNIFESP]
Barros, Sahana W. [UNIFESP]
Pinheiro, Luiz Fernando Muniz [UNIFESP]
Carvalho, Antonio Carlos [UNIFESP]
Fonseca, Francisco Antonio Helfenstein [UNIFESP]
dc.subject.por.fl_str_mv Insulin resistance
metabolic syndrome
acute coronary syndrome
diabetes mellitus, type 2
insulin-secreting cells
Resistência à insulina
síndrome metabólica
síndrome coronariana aguda
diabetes mellitus tipo 2
células secretoras de insulina
topic Insulin resistance
metabolic syndrome
acute coronary syndrome
diabetes mellitus, type 2
insulin-secreting cells
Resistência à insulina
síndrome metabólica
síndrome coronariana aguda
diabetes mellitus tipo 2
células secretoras de insulina
description BACKGROUND: Patients with metabolic syndrome (MetS) are at high coronary risk and beta-cell dysfunction or insulin resistance might predict an additional risk for early cardiovascular events. OBJECTIVE: This study aimed to evaluate early glucometabolic alterations in patients with MetS, but without previously known type 2 diabetes, after acute coronary syndrome. METHODS: A total of 114 patients were submitted to an oral glucose tolerance test (OGTT) 1-3 days after hospital discharge due to myocardial infarction or unstable angina. Based on the OGTT, we defined three groups of patients: normal glucose tolerance (NGT; n=26), impaired glucose tolerance (IGT; n=39), or diabetes (DM; n=49). The homeostasis model assessment (HOMA-IR) was used to measure insulin resistance; beta-cell responsiveness was assessed by the insulinogenic index at 30 min (ΔI30/ΔG30). RESULTS: Based on the HOMA-IR, patients with DM were more insulin-resistant than those with NGT or IGT (p<0.001). According to the insulinogenic index, the beta-cell responsiveness was also impaired in subjects with DM (p<0.001 vs NGT or IGT). CONCLUSION: High rates of glucometabolic alterations were found after acute coronary syndrome in patients with MetS. As these abnormalities markedly increase the risk for adverse outcomes, early OGTT among MetS patients might be used to identify those at the highest coronary risk.
publishDate 2009
dc.date.none.fl_str_mv 2009-02-01
2015-06-14T13:39:04Z
2015-06-14T13:39:04Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0066-782X2009000200004
Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 92, n. 2, p. 94-99, 2009.
10.1590/S0066-782X2009000200004
S0066-782X2009000200004-en.pdf
S0066-782X2009000200004-es.pdf
S0066-782X2009000200004-pt.pdf
0066-782X
S0066-782X2009000200004
http://repositorio.unifesp.br/handle/11600/4890
WOS:000265050600004
url http://dx.doi.org/10.1590/S0066-782X2009000200004
http://repositorio.unifesp.br/handle/11600/4890
identifier_str_mv Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 92, n. 2, p. 94-99, 2009.
10.1590/S0066-782X2009000200004
S0066-782X2009000200004-en.pdf
S0066-782X2009000200004-es.pdf
S0066-782X2009000200004-pt.pdf
0066-782X
S0066-782X2009000200004
WOS:000265050600004
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Arquivos Brasileiros de Cardiologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 94-99
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
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
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