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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...

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