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Published on: April 1, 2019
The -844 G>A PAI-1 polymorphism is associated with acute coronary syndrome in Mexican population
Ilian Janet García-González1, Yeminia Valle2, Elena Sandoval-Pinto3
1Instituto de Investigación en Ciencias Biomédicas, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, 44350 Guadalajara, JAL, Mexico ; Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, 44350 Guadalajara, JAL, Mexico.
Insights
The -844 G>A polymorphism in the plasminogen activator inhibitor-1 (PAI-1) gene is associated with an increased risk of acute coronary syndrome (ACS). The A allele and AA genotype are identified as risk factors for ACS and potentially dyslipidemia.
Area of Science:
- Genetics
- Cardiovascular Medicine
- Molecular Biology
Background:
- Acute coronary syndrome (ACS) poses a significant public health challenge due to high morbidity and mortality.
- Prothrombotic and proinflammatory states are key in ACS pathogenesis.
- Plasminogen activator inhibitor-1 (PAI-1) regulates fibrinolysis and immune responses.
Purpose of the Study:
- To investigate the association between the -844 G>A PAI-1 gene polymorphism and ACS.
- To determine if this polymorphism influences PAI-1 protein levels, contributing to ACS risk.
Main Methods:
- A case-control study involving 646 individuals from Western Mexico.
- Included 350 healthy controls and 296 patients diagnosed with ACS.
- Genotyping for the -844 G>A PAI-1 polymorphism was performed.
Main Results:
- Hypertension and smoking were the primary risk factors identified in the study population.
- The A allele (OR=1.27, P=0.04) and AA genotype (OR=1.86, P=0.02) of the -844 G>A polymorphism were significantly associated with ACS.
- Recessive model analysis confirmed the association (OR=1.76, P=0.02).
- A significant association was also found between the polymorphism and dyslipidemia in ACS patients (OR=1.99, P=0.04).
Conclusions:
- The A allele and AA genotype of the -844 PAI-1 gene polymorphism are confirmed risk factors for ACS.
- The AA genotype may play a role in the development of dyslipidemia among ACS patients.
- This genetic variant represents a potential biomarker for ACS risk stratification.
Background:
Acute coronary syndrome (ACS) has an important impact in public health with high morbidity and mortality. Prothrombotic and proinflammatory states are involved in the pathogenesis of the disease. Plasminogen activator inhibitor-1 (PAI-1) is the major inhibitor of the fibrinolysis and also is part of immune response. The -844 G>A gene polymorphism is related to increased PAI-1 protein levels. The aim of the study is to evaluate the association of -844 G>A PAI-1 polymorphism with ACS.
Methods:
A total of 646 individuals were recruited from Western Mexico: 350 unrelated healthy subjects and 296 patients with diagnosis of ACS.
Results:
The most important risk factor in our population was hypertension, followed by smoking. The genetic distribution showed an association of the A allele (OR = 1.27, P = 0.04) and AA genotype (OR = 1.86, P = 0.02) with ACS. The recessive model displayed similar results (OR = 1.76, P = 0.02). As additional finding, we observed significant differences in the genetic distribution of ACS dyslipidemic patients (OR = 1.99, P = 0.04). The A allele and AA genotype of -844 polymorphism of PAI-1 gene are risk factors for ACS. The AA genotype might be associated with the development of dyslipidemia in ACS patients.
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