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Published on: July 3, 2018
Aspects of the molecular-genetic profile in patients with ischemic heart disease
Natalia Caproş1, N Barbacar2, V Istrati1
1Institute of Genetics and Plant Physiology, Academy of Science, Chişinau, Republic of Moldova.
Insights
Genetic markers like the ACE gene DD genotype and D allele are linked to higher risk of ischemic heart disease (IHD) and myocardial infarction. The GPIIb/IIIa A2A2 haplotype is also associated with IHD susceptibility.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Ischemic Heart Disease Research
Background:
- Ischemic heart disease (IHD) poses a significant global health burden.
- Understanding the genetic underpinnings of IHD is crucial for risk stratification and prevention.
- Previous studies have implicated various genetic polymorphisms in IHD susceptibility.
Purpose of the Study:
- To investigate the clinical and molecular-genetic factors associated with different forms of ischemic heart disease.
- To identify specific gene polymorphisms that may serve as risk markers for IHD.
Main Methods:
- A case-control study involving 405 patients with acute coronary episodes.
- Analysis of polymorphisms in candidate genes: angiotensin converting enzyme (ACE), angiotensin II type 1 receptors (AT1R), endothelial nitric oxide synthase (eNOS), and platelet GPIIb/IIIa receptors (PlA1/PlA2).
- Genotyping performed using amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP).
Main Results:
- Significant differences in the frequency of the D risk allele of the ACE gene were observed between coronary patients and controls (78.65% vs. 61.24%, p < 0.05).
- The distribution of angiotensin II type 1 receptor A1166C gene polymorphism in IHD patients was: AA genotype (25.74%), CC genotype (16.78%), and CA genotype (59.28%).
Conclusions:
- The GPIIb/IIIa A2A2 gene haplotype is associated with increased susceptibility to IHD and a higher prevalence of dyslipidemia, especially in smokers.
- Carriage of the DD genotype and D allele of the ACE gene are potential markers for increased risk of IHD and myocardial infarction (MI).
- These genetic factors are also linked to elevated blood pressure.
Aim:
To assess the clinical and molecular-genetic aspects in patients with various forms of ischemic heart disease (IHD).
Material And Methods:
This case-control study was conducted in the interval 2007-2011 and included 405 patients with acute coronary episodes admitted to the Chisinau "Sfanta Treime" Municipal Hospital and Institute of Cardiology. Polymorphism of candidate genes angiotensin converting enzyme (ACE), angiotensin II type 1 receptors (AT1R), endothelial nitric oxide synthase (eNOS), and platelet GPIIb/IIIa receptors (PlA1/PlA2) were identified by amplified fragment length (AFLP) and restriction fragment length polymorphism (RFLP).
Results:
There were significant differences in the frequency of D risk alleles in coronary patients compared with controls (78.65% vs. 61.24%, p < 0.05). The distribution of angiotensin II type 1 receptor A1166C gene polymorphism in the group of patients with IHD was: AA genotype--72 (25.74%), CC genotype--47 (16.78%), CA genotype--161 (59.28%) patients.
Conclusions:
GPIIb/IIIa A2A2 gene haplotype is associated with susceptibility to IHD and increased prevalence of dyslipidemia, particularly in smokers. The carrier state of DD genotype and D allele of ACE gene can be used as markers of increased risk for IHD and myocardial infarction (MI) and is associated with increased blood pressure.
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