Key result
The presence of the eNOS GT + TT genotype was associated with a 2.1-fold increased risk of coronary artery disease (P=0.006).
Why the study?
Does the eNOS G894T gene variant increase the risk of coronary artery disease?
Population
299 individuals from Western Iran, comprising 207 unrelated patients with coronary artery disease and 92…
Comparison
Presence of endothelial nitric oxide synthase… vs Absence of the variant (GG genotype or G allele)
Design
Case-control
Authors
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Does not support eNOS genotyping in practice; leaves open its role in CAD risk assessment beyond this population.
Case-Control (n=299)
Does the eNOS G894T gene variant increase the risk of coronary artery disease?
Odds Ratio: 2.1
p-value: p=0.006
The eNOS G894T polymorphism (specifically the T allele and GT+TT genotypes) is significantly associated with an increased risk of coronary artery disease in the Western Iranian population.
Rahimi et al. (2011) conducted a case-control in Coronary Artery Disease (n=299). eNOS G894T variant (GT + TT genotype) vs. Absence of GT + TT genotype was evaluated on Risk of coronary artery disease (OR 2.1, p=0.006). The presence of the eNOS GT + TT genotype was associated with a 2.1-fold increased risk of coronary artery disease (P=0.006).
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