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Published on: June 20, 2020
Association Between ACE Gene Polymorphism and QT Dispersion in Patients with Acute Myocardial Infarction.
Zulkuf Karahan1, Murat Ugurlu1, Berzal Ucaman1
1Gazi Yasargil Education and Research Hospital, Cardiology, Diyarbakir, Turkey.
The ACE gene D allele may be linked to prolonged QT dispersion after myocardial infarction (MI). This suggests a potential interaction between genetic factors and heart rhythm abnormalities in MI patients.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Angiotensin converting enzyme (ACE) gene polymorphism is linked to the renin-angiotensin system, myocardial fibrosis, and ventricular repolarization abnormalities.
- Previous research suggests a connection between ACE gene variations and cardiovascular conditions.
Purpose of the Study:
- To investigate the association between the ACE gene insertion/deletion (I/D) polymorphism and QT dispersion in patients following acute myocardial infarction (MI).
Main Methods:
- The study involved 108 acute MI patients.
- Genomic DNA was analyzed for ACE gene I/D polymorphism.
- Electrocardiograms (ECGs) were recorded at baseline and 6-month follow-up to calculate QT dispersion.
Main Results:
- Patients with the DD genotype showed longer baseline QT dispersion compared to II or DI genotypes.
- At 6-month follow-up, DI genotype patients exhibited longer QT dispersion than DD or II genotypes.
- Carriers of the ACE D allele demonstrated a higher magnitude of QT dispersion prolongation at both baseline and 6-month follow-up.
Conclusions:
- The D allele of the ACE gene I/D polymorphism may be associated with QT dispersion prolongation in MI patients.
- This interaction could potentially elevate serum type I-C terminal pro-collagen, leading to myocardial fibrosis and increased action potential duration.
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