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Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation

Background. Thrombin has been implicated as a key molecule in atherosclerotic progression. Clinical evidence shows that thrombin generation is enhanced in atherosclerosis, but its role as a risk factor for coronary atherosclerotic burden has not been proven in coronary artery disease (CAD) stable pa...

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Autores principales: Valente-Acosta, Benjamin, Baños-González, Manuel Alfonso, Peña-Duque, Marco Antonio, Martínez-Ríos, Marco Antonio, Quintanar-Trejo, Leslie, Aptilon-Duque, Gad, Flores-García, Mirthala, Cruz-Robles, David, Cardoso-Saldaña, Guillermo, de la Peña-Díaz, Aurora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997082/
https://www.ncbi.nlm.nih.gov/pubmed/27597926
http://dx.doi.org/10.1155/2016/5149825
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author Valente-Acosta, Benjamin
Baños-González, Manuel Alfonso
Peña-Duque, Marco Antonio
Martínez-Ríos, Marco Antonio
Quintanar-Trejo, Leslie
Aptilon-Duque, Gad
Flores-García, Mirthala
Cruz-Robles, David
Cardoso-Saldaña, Guillermo
de la Peña-Díaz, Aurora
author_facet Valente-Acosta, Benjamin
Baños-González, Manuel Alfonso
Peña-Duque, Marco Antonio
Martínez-Ríos, Marco Antonio
Quintanar-Trejo, Leslie
Aptilon-Duque, Gad
Flores-García, Mirthala
Cruz-Robles, David
Cardoso-Saldaña, Guillermo
de la Peña-Díaz, Aurora
author_sort Valente-Acosta, Benjamin
collection PubMed
description Background. Thrombin has been implicated as a key molecule in atherosclerotic progression. Clinical evidence shows that thrombin generation is enhanced in atherosclerosis, but its role as a risk factor for coronary atherosclerotic burden has not been proven in coronary artery disease (CAD) stable patients. Objectives. To evaluate the association between TAT levels and homocysteine levels and the presence of coronary artery disease diagnosed by coronary angiography in patients with stable CAD. Methods and Results. We included 95 stable patients admitted to the Haemodynamics Department, including 63 patients with significant CAD and 32 patients without. We measured the thrombin-antithrombin complex (TAT) and homocysteine concentrations in all the patients. The CAD patients exhibited higher concentrations of TAT (40.76 μg/L versus 20.81 μg/L, p = 0.002) and homocysteine (11.36 μmol/L versus 8.81 μmol/L, p < 0.01) compared to the patients without significant CAD. Specifically, in patients with CAD+ the level of TAT level was associated with the severity of CAD being 36.17 ± 24.48 μg/L in the patients with bivascular obstruction and 42.77 ± 31.81 μg/L in trivascular coronary obstruction, p = 0.002. Conclusions. The level of in vivo thrombin generation, quantified as TAT complexes, is associated with the presence and severity of CAD assessed by coronary angiography in stable CAD patients.
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spelling pubmed-49970822016-09-05 Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation Valente-Acosta, Benjamin Baños-González, Manuel Alfonso Peña-Duque, Marco Antonio Martínez-Ríos, Marco Antonio Quintanar-Trejo, Leslie Aptilon-Duque, Gad Flores-García, Mirthala Cruz-Robles, David Cardoso-Saldaña, Guillermo de la Peña-Díaz, Aurora Cardiol Res Pract Research Article Background. Thrombin has been implicated as a key molecule in atherosclerotic progression. Clinical evidence shows that thrombin generation is enhanced in atherosclerosis, but its role as a risk factor for coronary atherosclerotic burden has not been proven in coronary artery disease (CAD) stable patients. Objectives. To evaluate the association between TAT levels and homocysteine levels and the presence of coronary artery disease diagnosed by coronary angiography in patients with stable CAD. Methods and Results. We included 95 stable patients admitted to the Haemodynamics Department, including 63 patients with significant CAD and 32 patients without. We measured the thrombin-antithrombin complex (TAT) and homocysteine concentrations in all the patients. The CAD patients exhibited higher concentrations of TAT (40.76 μg/L versus 20.81 μg/L, p = 0.002) and homocysteine (11.36 μmol/L versus 8.81 μmol/L, p < 0.01) compared to the patients without significant CAD. Specifically, in patients with CAD+ the level of TAT level was associated with the severity of CAD being 36.17 ± 24.48 μg/L in the patients with bivascular obstruction and 42.77 ± 31.81 μg/L in trivascular coronary obstruction, p = 0.002. Conclusions. The level of in vivo thrombin generation, quantified as TAT complexes, is associated with the presence and severity of CAD assessed by coronary angiography in stable CAD patients. Hindawi Publishing Corporation 2016 2016-08-11 /pmc/articles/PMC4997082/ /pubmed/27597926 http://dx.doi.org/10.1155/2016/5149825 Text en Copyright © 2016 Benjamin Valente-Acosta et al. https://creativecommons.org/licenses/by/4.0/ 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
Valente-Acosta, Benjamin
Baños-González, Manuel Alfonso
Peña-Duque, Marco Antonio
Martínez-Ríos, Marco Antonio
Quintanar-Trejo, Leslie
Aptilon-Duque, Gad
Flores-García, Mirthala
Cruz-Robles, David
Cardoso-Saldaña, Guillermo
de la Peña-Díaz, Aurora
Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title_full Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title_fullStr Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title_full_unstemmed Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title_short Association between Stable Coronary Artery Disease and In Vivo Thrombin Generation
title_sort association between stable coronary artery disease and in vivo thrombin generation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997082/
https://www.ncbi.nlm.nih.gov/pubmed/27597926
http://dx.doi.org/10.1155/2016/5149825
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