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Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease
BACKGROUND: To evaluate the macrophage migration inhibitory factor and E-selectin levels in patients with acute coronary syndrome. MATERIALS/METHODS: We examined the plasma migration inhibitory factor and E-selectin levels in 87 patients who presented with chest pain at our hospital. The patients we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculdade de Medicina / USP
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449471/ https://www.ncbi.nlm.nih.gov/pubmed/26017646 http://dx.doi.org/10.6061/clinics/2015(03)03 |
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author | Yüksel, Arif Bilgir, Ferda Bilgir, Oktay Calan, Mehmet Bozkaya, Giray |
author_facet | Yüksel, Arif Bilgir, Ferda Bilgir, Oktay Calan, Mehmet Bozkaya, Giray |
author_sort | Yüksel, Arif |
collection | PubMed |
description | BACKGROUND: To evaluate the macrophage migration inhibitory factor and E-selectin levels in patients with acute coronary syndrome. MATERIALS/METHODS: We examined the plasma migration inhibitory factor and E-selectin levels in 87 patients who presented with chest pain at our hospital. The patients were classified into two groups according to their cardiac status. Sixty-five patients had acute myocardial infarction, and 22 patients had non-cardiac chest pain (non-coronary disease). We designated the latter group of patients as the control group. The patients who presented with acute myocardial infarction were further divided into two subgroups: ST-elevated myocardial infarction (n = 30) and non-ST elevated myocardial infarction (n = 35). RESULTS: We found higher plasma migration inhibitory factor levels in both acute myocardial infarction subgroups than in the control group. However, the E-selectin levels were similar between the acute myocardial infarction and control patients. In addition, we did not find a significant difference in the plasma migration inhibitory factor levels between the ST elevated myocardial infarction and NST-elevated myocardial infarction subgroups. DISCUSSION: The circulating concentrations of migration inhibitory factor were significantly increased in acute myocardial infarction patients, whereas the soluble E-selectin levels were similar between acute myocardial infarction patients and control subjects. Our results suggest that migration inhibitory factor may play a role in the atherosclerotic process. |
format | Online Article Text |
id | pubmed-4449471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Faculdade de Medicina / USP |
record_format | MEDLINE/PubMed |
spelling | pubmed-44494712015-07-08 Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease Yüksel, Arif Bilgir, Ferda Bilgir, Oktay Calan, Mehmet Bozkaya, Giray Clinics (Sao Paulo) Clinical Science BACKGROUND: To evaluate the macrophage migration inhibitory factor and E-selectin levels in patients with acute coronary syndrome. MATERIALS/METHODS: We examined the plasma migration inhibitory factor and E-selectin levels in 87 patients who presented with chest pain at our hospital. The patients were classified into two groups according to their cardiac status. Sixty-five patients had acute myocardial infarction, and 22 patients had non-cardiac chest pain (non-coronary disease). We designated the latter group of patients as the control group. The patients who presented with acute myocardial infarction were further divided into two subgroups: ST-elevated myocardial infarction (n = 30) and non-ST elevated myocardial infarction (n = 35). RESULTS: We found higher plasma migration inhibitory factor levels in both acute myocardial infarction subgroups than in the control group. However, the E-selectin levels were similar between the acute myocardial infarction and control patients. In addition, we did not find a significant difference in the plasma migration inhibitory factor levels between the ST elevated myocardial infarction and NST-elevated myocardial infarction subgroups. DISCUSSION: The circulating concentrations of migration inhibitory factor were significantly increased in acute myocardial infarction patients, whereas the soluble E-selectin levels were similar between acute myocardial infarction patients and control subjects. Our results suggest that migration inhibitory factor may play a role in the atherosclerotic process. Faculdade de Medicina / USP 2015-03 2015-03 /pmc/articles/PMC4449471/ /pubmed/26017646 http://dx.doi.org/10.6061/clinics/2015(03)03 Text en Copyright © 2015 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Yüksel, Arif Bilgir, Ferda Bilgir, Oktay Calan, Mehmet Bozkaya, Giray Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title | Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title_full | Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title_fullStr | Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title_full_unstemmed | Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title_short | Increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
title_sort | increased circulating macrophage migration inhibitory factor levels are associated with coronary artery disease |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449471/ https://www.ncbi.nlm.nih.gov/pubmed/26017646 http://dx.doi.org/10.6061/clinics/2015(03)03 |
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