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En Face Detection of Nitric Oxide and Superoxide in Endothelial Layer of Intact Arteries
Published on: February 25, 2016
Nitric Oxide Synthase 3 Gene Polymorphisms and Their Association with Acute Myocardial Infarction and Chronic Stable
Sunil Kumar1, Deepak Juyal2, Arun Pandey3
1Department of Microbiology, Veer Chandra Singh Garhwali Government Institute of Medical Science and Research, Srinagar, Uttarakhand, India.
Genetic variations in the NOS3 gene, specifically the 894G/T polymorphism, are linked to coronary artery disease (CAD) risk. Lower nitric oxide (NO) levels are also associated with CAD in the North Indian population.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Atherosclerosis Research
Background:
- Coronary artery disease (CAD), including acute myocardial infarction (AMI) and chronic stable angina (CSA), has known risk factors, with genetic predispositions playing a significant role.
- The nitric oxide synthase 3 (NOS3) gene, crucial for nitric oxide (NO) production, is important in regulating atherosclerosis and preventing CAD.
Purpose of the Study:
- To investigate the association of three NOS3 gene polymorphisms (-786C/T, 894G/T, and 4a4b) with CAD, specifically AMI and CSA.
- To compare the prevalence of these polymorphisms and plasma nitric oxide metabolite (NOx) levels between CAD patients and healthy controls.
Main Methods:
- Genotyping of 100 AMI patients, 100 CSA patients, and 100 healthy controls for NOS3 polymorphisms using polymerase chain reaction-restriction fragment length polymorphism.
- Measurement of plasma NOx levels in all study participants.
Main Results:
- A significant association was found between the 894G/T NOS3 polymorphism and AMI (dominant model, P=0.052) and CSA (dominant and codominant models, P=0.008, P=0.006).
- Plasma NOx levels were significantly lower in both AMI (37.05 ± 6.75) and CSA (38.67 ± 5.61) patients compared to healthy controls (43.80 ± 6.28).
- No significant association was detected for the -786C/T and 4a4b NOS3 polymorphisms with AMI or CSA risk.
Conclusions:
- The 894G/T NOS3 polymorphism is significantly associated with AMI and CSA in the North Indian population.
- Plasma NOx levels are independently associated with CAD, highlighting their role in disease development.
- These findings contribute to identifying genetic risk factors for CAD and improving diagnostic and therapeutic strategies.
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