Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/146902 |
Resumo: | OBJECTIVES: Inflammatory molecules play a role in the development of atherosclerosis, which is the primary origin of cardiovascular disorders. However, to the best of our knowledge, no study has attempted to investigate the relationship between these circulating molecules and the prediction of cardiovascular risk. The present study aimed to investigate the relationships of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 serum concentrations with the extent of coronary lesions. METHODS: Seventy-four individuals who were undergoing coronary angiography for the first time for diagnostic purposes were enrolled in this study. The extent of the coronary lesion was assessed using the Friesinger Index, and subjects were classified into four groups: no lesions, minor lesions, intermediate lesions and major lesions. Serum biochemical parameters and serum concentrations of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 were analyzed. RESULTS: The vascular cell adhesion molecule-1 concentration was higher than 876 ng/mL in individuals with intermediate and major lesions (p |
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Clinics |
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Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesionsVCAM-1Cardiovascular DiseasesAtherosclerosisInflammatory MoleculesOBJECTIVES: Inflammatory molecules play a role in the development of atherosclerosis, which is the primary origin of cardiovascular disorders. However, to the best of our knowledge, no study has attempted to investigate the relationship between these circulating molecules and the prediction of cardiovascular risk. The present study aimed to investigate the relationships of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 serum concentrations with the extent of coronary lesions. METHODS: Seventy-four individuals who were undergoing coronary angiography for the first time for diagnostic purposes were enrolled in this study. The extent of the coronary lesion was assessed using the Friesinger Index, and subjects were classified into four groups: no lesions, minor lesions, intermediate lesions and major lesions. Serum biochemical parameters and serum concentrations of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 were analyzed. RESULTS: The vascular cell adhesion molecule-1 concentration was higher than 876 ng/mL in individuals with intermediate and major lesions (pHospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2018-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/14690210.6061/clinics/2018/e203Clinics; Vol. 73 (2018); e203Clinics; v. 73 (2018); e203Clinics; Vol. 73 (2018); e2031980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/146902/140437Copyright (c) 2018 Clinicsinfo:eu-repo/semantics/openAccessSantos, Jéssica Cavalcante dosCruz, Marina SampaioBortolin, Raul HernandesOliveira, Katiene Macêdo deAraújo, Jéssica Nayara Góes deDuarte, Victor Hugo RezendeSilva, Ananília Medeiros Gomes daSantos, Isabelle Cristina Clemente dosDantas, Juliana Marinho de OliveiraPaiva, Maria Sanali Moura de OliveiraRezende, Adriana AugustoHirata, Mario HiroyukiHirata, Rosario Dominguez CrespoLuchessi, André DucatiSilbiger, Vivian Nogueira2019-05-14T11:48:50Zoai:revistas.usp.br:article/146902Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-05-14T11:48:50Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
title |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
spellingShingle |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions Santos, Jéssica Cavalcante dos VCAM-1 Cardiovascular Diseases Atherosclerosis Inflammatory Molecules |
title_short |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
title_full |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
title_fullStr |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
title_full_unstemmed |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
title_sort |
Relationship between circulating VCAM-1, ICAM-1, E-selectin and MMP9 and the extent of coronary lesions |
author |
Santos, Jéssica Cavalcante dos |
author_facet |
Santos, Jéssica Cavalcante dos Cruz, Marina Sampaio Bortolin, Raul Hernandes Oliveira, Katiene Macêdo de Araújo, Jéssica Nayara Góes de Duarte, Victor Hugo Rezende Silva, Ananília Medeiros Gomes da Santos, Isabelle Cristina Clemente dos Dantas, Juliana Marinho de Oliveira Paiva, Maria Sanali Moura de Oliveira Rezende, Adriana Augusto Hirata, Mario Hiroyuki Hirata, Rosario Dominguez Crespo Luchessi, André Ducati Silbiger, Vivian Nogueira |
author_role |
author |
author2 |
Cruz, Marina Sampaio Bortolin, Raul Hernandes Oliveira, Katiene Macêdo de Araújo, Jéssica Nayara Góes de Duarte, Victor Hugo Rezende Silva, Ananília Medeiros Gomes da Santos, Isabelle Cristina Clemente dos Dantas, Juliana Marinho de Oliveira Paiva, Maria Sanali Moura de Oliveira Rezende, Adriana Augusto Hirata, Mario Hiroyuki Hirata, Rosario Dominguez Crespo Luchessi, André Ducati Silbiger, Vivian Nogueira |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Santos, Jéssica Cavalcante dos Cruz, Marina Sampaio Bortolin, Raul Hernandes Oliveira, Katiene Macêdo de Araújo, Jéssica Nayara Góes de Duarte, Victor Hugo Rezende Silva, Ananília Medeiros Gomes da Santos, Isabelle Cristina Clemente dos Dantas, Juliana Marinho de Oliveira Paiva, Maria Sanali Moura de Oliveira Rezende, Adriana Augusto Hirata, Mario Hiroyuki Hirata, Rosario Dominguez Crespo Luchessi, André Ducati Silbiger, Vivian Nogueira |
dc.subject.por.fl_str_mv |
VCAM-1 Cardiovascular Diseases Atherosclerosis Inflammatory Molecules |
topic |
VCAM-1 Cardiovascular Diseases Atherosclerosis Inflammatory Molecules |
description |
OBJECTIVES: Inflammatory molecules play a role in the development of atherosclerosis, which is the primary origin of cardiovascular disorders. However, to the best of our knowledge, no study has attempted to investigate the relationship between these circulating molecules and the prediction of cardiovascular risk. The present study aimed to investigate the relationships of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 serum concentrations with the extent of coronary lesions. METHODS: Seventy-four individuals who were undergoing coronary angiography for the first time for diagnostic purposes were enrolled in this study. The extent of the coronary lesion was assessed using the Friesinger Index, and subjects were classified into four groups: no lesions, minor lesions, intermediate lesions and major lesions. Serum biochemical parameters and serum concentrations of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin and matrix metalloproteinase 9 were analyzed. RESULTS: The vascular cell adhesion molecule-1 concentration was higher than 876 ng/mL in individuals with intermediate and major lesions (p |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-01-01 |
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/146902 10.6061/clinics/2018/e203 |
url |
https://www.revistas.usp.br/clinics/article/view/146902 |
identifier_str_mv |
10.6061/clinics/2018/e203 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/146902/140437 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2018 Clinics info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2018 Clinics |
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. 73 (2018); e203 Clinics; v. 73 (2018); e203 Clinics; Vol. 73 (2018); e203 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_ |
1800222763701501952 |