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Relationship between the -374T/A RAGE gene polymorphism and angiographic coronary artery disease
- Source :
- Europe PubMed Central, Scopus-Elsevier, Publons
-
Abstract
- The receptor for advanced glycation end products (RAGE) is thought to play a critical role in diabetic atherosclerosis. Accordingly, a functional -374T/A polymorphism in RAGE gene promoter has been associated with macrovascular complications in type 1 diabetic patients. However, the extent to which this common variant influences the risk of coronary artery disease (CAD) in the general population remains to be determined. We genotyped the -374T/A RAGE polymorphism in 259 non-diabetic individuals, of whom 175 had angiographically documented coronary artery disease (CAD patients) and 84 had normal coronary angiography (CAD-free control subjects). Homozygosity for the -374A allele was found in 9.7% of the CAD patients versus 22.6% of the CAD-free subjects (p=0.005). By means of a multiple logistic regression analysis, the AA genotype of the -374T/A polymorphism was shown to be independently associated with a reduced risk of CAD (adjusted odds ratio 0.33, 95% CI 0.15 to 0.73; p=0.006). Our observations suggest that the -374T/A polymorphism of the RAGE gene may reduce susceptibility to CAD, thus exerting a protective effect on coronary risk. Future pathophysiological studies may be worthwhile to clarify the mechanisms behind this association.
- Subjects :
- Male
medicine.medical_specialty
Pathology
Adenosine
Genotype
Receptor for Advanced Glycation End Products
Population
Coronary Artery Disease
Coronary Angiography
Coronary artery disease
Internal medicine
Genetics
medicine
Humans
Genetic Predisposition to Disease
cardiovascular diseases
Receptors, Immunologic
Allele
education
Alleles
education.field_of_study
Polymorphism, Genetic
business.industry
General Medicine
Odds ratio
Middle Aged
medicine.disease
Molecular medicine
Pathophysiology
Cardiology
Female
Gene polymorphism
business
Thymidine
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Europe PubMed Central, Scopus-Elsevier, Publons
- Accession number :
- edsair.doi.dedup.....971bcb9d5013fc4896bab5f53208702a