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The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population
Background. Acute coronary syndrome (ACS) has an important impact in public health with high morbidity and mortality. Prothrombotic and proinflammatory states are involved in the pathogenesis of the disease. Plasminogen activator inhibitor-1 (PAI-1) is the major inhibitor of the fibrinolysis and als...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350946/ https://www.ncbi.nlm.nih.gov/pubmed/25788758 http://dx.doi.org/10.1155/2015/460974 |
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author | García-González, Ilian Janet Valle, Yeminia Sandoval-Pinto, Elena Valdés-Alvarado, Emmanuel Valdez-Haro, Angélica Francisco Muñoz-Valle, José Flores-Salinas, Héctor Enrique Figuera-Villanueva, Luis Eduardo Dávalos-Rodríguez, Nory Omayra Padilla-Gutiérrez, Jorge Ramón |
author_facet | García-González, Ilian Janet Valle, Yeminia Sandoval-Pinto, Elena Valdés-Alvarado, Emmanuel Valdez-Haro, Angélica Francisco Muñoz-Valle, José Flores-Salinas, Héctor Enrique Figuera-Villanueva, Luis Eduardo Dávalos-Rodríguez, Nory Omayra Padilla-Gutiérrez, Jorge Ramón |
author_sort | García-González, Ilian Janet |
collection | PubMed |
description | Background. Acute coronary syndrome (ACS) has an important impact in public health with high morbidity and mortality. Prothrombotic and proinflammatory states are involved in the pathogenesis of the disease. Plasminogen activator inhibitor-1 (PAI-1) is the major inhibitor of the fibrinolysis and also is part of immune response. The -844 G>A gene polymorphism is related to increased PAI-1 protein levels. The aim of the study is to evaluate the association of -844 G>A PAI-1 polymorphism with ACS. Methods. A total of 646 individuals were recruited from Western Mexico: 350 unrelated healthy subjects and 296 patients with diagnosis of ACS. Results. The most important risk factor in our population was hypertension, followed by smoking. The genetic distribution showed an association of the A allele (OR = 1.27, P = 0.04) and AA genotype (OR = 1.86, P = 0.02) with ACS. The recessive model displayed similar results (OR = 1.76, P = 0.02). As additional finding, we observed significant differences in the genetic distribution of ACS dyslipidemic patients (OR = 1.99, P = 0.04). The A allele and AA genotype of -844 polymorphism of PAI-1 gene are risk factors for ACS. The AA genotype might be associated with the development of dyslipidemia in ACS patients. |
format | Online Article Text |
id | pubmed-4350946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43509462015-03-18 The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population García-González, Ilian Janet Valle, Yeminia Sandoval-Pinto, Elena Valdés-Alvarado, Emmanuel Valdez-Haro, Angélica Francisco Muñoz-Valle, José Flores-Salinas, Héctor Enrique Figuera-Villanueva, Luis Eduardo Dávalos-Rodríguez, Nory Omayra Padilla-Gutiérrez, Jorge Ramón Dis Markers Research Article Background. Acute coronary syndrome (ACS) has an important impact in public health with high morbidity and mortality. Prothrombotic and proinflammatory states are involved in the pathogenesis of the disease. Plasminogen activator inhibitor-1 (PAI-1) is the major inhibitor of the fibrinolysis and also is part of immune response. The -844 G>A gene polymorphism is related to increased PAI-1 protein levels. The aim of the study is to evaluate the association of -844 G>A PAI-1 polymorphism with ACS. Methods. A total of 646 individuals were recruited from Western Mexico: 350 unrelated healthy subjects and 296 patients with diagnosis of ACS. Results. The most important risk factor in our population was hypertension, followed by smoking. The genetic distribution showed an association of the A allele (OR = 1.27, P = 0.04) and AA genotype (OR = 1.86, P = 0.02) with ACS. The recessive model displayed similar results (OR = 1.76, P = 0.02). As additional finding, we observed significant differences in the genetic distribution of ACS dyslipidemic patients (OR = 1.99, P = 0.04). The A allele and AA genotype of -844 polymorphism of PAI-1 gene are risk factors for ACS. The AA genotype might be associated with the development of dyslipidemia in ACS patients. Hindawi Publishing Corporation 2015 2015-02-19 /pmc/articles/PMC4350946/ /pubmed/25788758 http://dx.doi.org/10.1155/2015/460974 Text en Copyright © 2015 Ilian Janet García-González et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article García-González, Ilian Janet Valle, Yeminia Sandoval-Pinto, Elena Valdés-Alvarado, Emmanuel Valdez-Haro, Angélica Francisco Muñoz-Valle, José Flores-Salinas, Héctor Enrique Figuera-Villanueva, Luis Eduardo Dávalos-Rodríguez, Nory Omayra Padilla-Gutiérrez, Jorge Ramón The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title | The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title_full | The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title_fullStr | The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title_full_unstemmed | The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title_short | The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population |
title_sort | -844 g>a pai-1 polymorphism is associated with acute coronary syndrome in mexican population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350946/ https://www.ncbi.nlm.nih.gov/pubmed/25788758 http://dx.doi.org/10.1155/2015/460974 |
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