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Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease
Background. Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine. This study explored the association of 173G/C polymorphism of the MIF gene with coronary heart disease (CHD). Methods. Sequencing was carried out after polymerase chain reaction with DNA specimens from 186 volunt...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364024/ https://www.ncbi.nlm.nih.gov/pubmed/25821795 http://dx.doi.org/10.1155/2015/315174 |
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author | Ji, Kangting Wang, Xiaoyan Li, Ji Lu, Qin Wang, Guoqiang Xue, Yangjing Zhang, Suqin Qian, Lu Wu, Wenwu Zhu, Yongjin Wang, Luping Liao, Lianming Tang, Jifei |
author_facet | Ji, Kangting Wang, Xiaoyan Li, Ji Lu, Qin Wang, Guoqiang Xue, Yangjing Zhang, Suqin Qian, Lu Wu, Wenwu Zhu, Yongjin Wang, Luping Liao, Lianming Tang, Jifei |
author_sort | Ji, Kangting |
collection | PubMed |
description | Background. Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine. This study explored the association of 173G/C polymorphism of the MIF gene with coronary heart disease (CHD). Methods. Sequencing was carried out after polymerase chain reaction with DNA specimens from 186 volunteers without CHD and 70 patients with CHD. Plasma MIF levels on admission were measured by ELISA. Patients were classified into either stable angina pectoris (SAP) or unstable angina pectoris (UAP). Genotype distribution between cases and controls and the association of patients' genotypes with MIF level and plaque stability were statistically evaluated (ethical approval number: 2012-01). Results. The frequency of the C genotype was higher in CHD patients than in the control (P = 0.014). The frequency of the 173(*)CC genotype was higher in CHD patients than in the control (P = 0.005). The plasma MIF level was higher in MIF173(*)C carriers than in MIF173(*)G carriers (P = 0.033). CHD patients had higher plasma MIF levels than the control (P = 0.000). Patients with UAP had higher plasma MIF levels than patients with SAP (P = 0.014). Conclusions. These data suggest that MIF −173G/C polymorphism may be related to the development of CHD in a Chinese population. Plasma MIF level is a predictor of plaque stability. This trial is registered with NCT01750502 . |
format | Online Article Text |
id | pubmed-4364024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43640242015-03-29 Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease Ji, Kangting Wang, Xiaoyan Li, Ji Lu, Qin Wang, Guoqiang Xue, Yangjing Zhang, Suqin Qian, Lu Wu, Wenwu Zhu, Yongjin Wang, Luping Liao, Lianming Tang, Jifei Biomed Res Int Research Article Background. Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine. This study explored the association of 173G/C polymorphism of the MIF gene with coronary heart disease (CHD). Methods. Sequencing was carried out after polymerase chain reaction with DNA specimens from 186 volunteers without CHD and 70 patients with CHD. Plasma MIF levels on admission were measured by ELISA. Patients were classified into either stable angina pectoris (SAP) or unstable angina pectoris (UAP). Genotype distribution between cases and controls and the association of patients' genotypes with MIF level and plaque stability were statistically evaluated (ethical approval number: 2012-01). Results. The frequency of the C genotype was higher in CHD patients than in the control (P = 0.014). The frequency of the 173(*)CC genotype was higher in CHD patients than in the control (P = 0.005). The plasma MIF level was higher in MIF173(*)C carriers than in MIF173(*)G carriers (P = 0.033). CHD patients had higher plasma MIF levels than the control (P = 0.000). Patients with UAP had higher plasma MIF levels than patients with SAP (P = 0.014). Conclusions. These data suggest that MIF −173G/C polymorphism may be related to the development of CHD in a Chinese population. Plasma MIF level is a predictor of plaque stability. This trial is registered with NCT01750502 . Hindawi Publishing Corporation 2015 2015-03-04 /pmc/articles/PMC4364024/ /pubmed/25821795 http://dx.doi.org/10.1155/2015/315174 Text en Copyright © 2015 Kangting Ji 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 Ji, Kangting Wang, Xiaoyan Li, Ji Lu, Qin Wang, Guoqiang Xue, Yangjing Zhang, Suqin Qian, Lu Wu, Wenwu Zhu, Yongjin Wang, Luping Liao, Lianming Tang, Jifei Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title | Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title_full | Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title_fullStr | Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title_full_unstemmed | Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title_short | Macrophage Migration Inhibitory Factor Polymorphism Is Associated with Susceptibility to Inflammatory Coronary Heart Disease |
title_sort | macrophage migration inhibitory factor polymorphism is associated with susceptibility to inflammatory coronary heart disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364024/ https://www.ncbi.nlm.nih.gov/pubmed/25821795 http://dx.doi.org/10.1155/2015/315174 |
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