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MIF gene rs755622 polymorphism positively associated with acute coronary syndrome in Chinese Han population:
Guo-Li Du1,2,3, Jun-Yi Luo1,4, Duolao Wang5
1State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Department of Cardiology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Abstract:
Macrophage migration inhibitory factor (MIF) has been recognized as a major player in the pathogenesis of atherosclerosis. This study determined the association between polymorphisms of MIF gene and acute coronary syndrome (ACS). The polymorphism of MIF gene (rs755622, rs1007888 and rs2096525) was analyzed in 1153 healthy controls and 699 ACS cases in Chinese Han population. Plasma MIF level was also measured in part of ACS patients (139/19.9%) and healthy controls (129/11.2%) randomly. Most participants including healthy controls and ACS patients carried rs755622 GG (63.1% vs. 56.7%) and CG genotypes (33.1% vs. 38.9%) and G allele of rs755622 (79.6% vs. 76.1%, respectively), while CC genotype (3.8% vs. 4.4%) and C allele (20.4% vs. 23.9%) carriers were the lowest. Multivariate logistic regression analysis showed that carriers with rs755622 C allele had a higher risk of ACS compared to other genotypes (AOR = 1.278, 95% CI: 1.042-1.567). In addition, CC genotype carriers had the highest plasma levels of MIF than other genotype carriers. The MIF level in ACS patients with CC genotype was significantly higher than ACS patients carrying GG genotype and healthy controls carrying 3 different genotypes of MIF gene rs755622. Our findings indicate that MIF gene rs755622 variant C allele is associated with increased risk of ACS. Identification of this MIF gene polymorphism may help for predicting the risk of ACS.
Insights
The macrophage migration inhibitory factor (MIF) gene variant rs755622 C allele is linked to a higher risk of acute coronary syndrome (ACS). This MIF gene polymorphism may aid in predicting ACS risk.
Area of Science:
- Cardiovascular Genetics
- Immunology
- Molecular Biology
Background:
- Macrophage migration inhibitory factor (MIF) plays a key role in atherosclerosis development.
- Genetic variations in the MIF gene may influence susceptibility to cardiovascular diseases.
Purpose of the Study:
- To investigate the association between MIF gene polymorphisms (rs755622, rs1007888, rs2096525) and acute coronary syndrome (ACS) in the Chinese Han population.
- To determine if plasma MIF levels correlate with specific MIF gene polymorphisms and ACS risk.
Main Methods:
- Genotyping of MIF gene polymorphisms (rs755622, rs1007888, rs2096525) in 1153 healthy controls and 699 ACS cases.
- Measurement of plasma MIF levels in a subset of ACS patients and healthy controls.
- Multivariate logistic regression analysis to assess the association between polymorphisms and ACS risk.
Main Results:
- Carriers of the rs755622 C allele exhibited a significantly higher risk of ACS (AOR = 1.278).
- Individuals with the rs755622 CC genotype showed the highest plasma MIF levels.
- Elevated plasma MIF levels were observed in ACS patients with the CC genotype compared to GG genotype carriers and healthy controls.
Conclusions:
- The C allele of the MIF gene rs755622 variant is associated with an increased risk of developing ACS.
- MIF gene rs755622 polymorphism may serve as a potential biomarker for predicting ACS risk.
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