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Published on: July 3, 2018
Genetic polymorphisms in preoperative myocardial infarction
Sefa Senol1, Mehmet Ugur Es2, Gökhan Gokmen3
1Department of Cardiovascular Surgery, Educational and Research Hospital, Elazig, Turkey ssenol2012@gmail.com.
Insights
Plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase gene polymorphisms were not associated with myocardial infarction with ST-segment elevation in patients undergoing coronary artery bypass grafting. These genetic factors did not prove to be risk factors in the studied population.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Thrombosis Research
Background:
- Myocardial infarction with ST-segment elevation (STEMI) is a critical cardiovascular event.
- Coronary artery bypass grafting (CABG) is a common revascularization strategy for STEMI.
- Genetic predispositions are increasingly investigated for cardiovascular disease risk.
Purpose of the Study:
- To investigate the association of plasminogen activator inhibitor 1 (PAI-1) and methylenetetrahydrofolate reductase (MTHFR) polymorphisms with STEMI.
- To compare PAI-1 and MTHFR C677T and A1298C allele frequencies in STEMI patients before CABG versus controls with prior CABG.
Main Methods:
- Real-time polymerase chain reaction (PCR) was used to determine genetic polymorphisms.
- A study group comprised 70 STEMI patients scheduled for CABG.
- A control group consisted of 70 patients with a history of CABG.
Main Results:
- No significant differences were observed in PAI-1 polymorphisms between the groups.
- MTHFR C677T and A1298C polymorphisms showed no significant differences between STEMI patients and controls.
- Allele frequencies for both PAI-1 and MTHFR polymorphisms were comparable between the two groups.
Conclusions:
- PAI-1 and MTHFR gene polymorphisms are not associated with STEMI in patients undergoing CABG.
- These specific genetic variations do not appear to be risk factors for STEMI in this patient cohort.
- Further research may explore other genetic markers in relation to STEMI and CABG outcomes.
Objective:
This study compared plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in patients with myocardial infarction with ST-segment elevation before undergoing to coronary artery bypass grafting, and in patients who had previously undergone coronary artery bypass grafting.
Method:
Seventy patients with myocardial infarction with ST-segment elevation, scheduled to undergo coronary artery bypass grafting, were included in the study group, and 70 patients who had previously undergone coronary artery bypass grafting were included in the control group. Genetic polymorphisms were determined using real-time polymerase chain reaction methods.
Results:
Our data showed that there were no significant differences in plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms or allele frequencies between the 2 groups.
Conclusion:
Plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms were not associated risk factors in patients who had myocardial infarction with ST-segment elevation and planned to have coronary artery bypass grafting.
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