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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
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.
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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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