Association of Polymorphisms of the Receptor for Advanced Glycation End Products Gene and Susceptibility to Sporadic Abdominal Aortic Aneurysm

• Published in: BioMed research international 2015-01, Vol.2015 (2015), p.1-10
• Main Authors: Wang, Haiyang, Li, Keshen, Li, Jingbo, Li, Hali, Jing, Bao, Li, You, Zhuang, Junli, Yao, Ye, Shao, Changgang
• Format: Article
• Language: English
• Subjects: Abdomen; Abdominal aneurysm; Advanced glycation end products; Age; Aged; Alleles; Alzheimer's disease; Aneurysms; Aortic Aneurysm, Abdominal - genetics; Case-Control Studies; Colleges & universities; Deoxyribonucleic acid; Disease susceptibility; DNA; Female; Gene Frequency - genetics; Genetic polymorphisms; Genetic Predisposition to Disease - genetics; Genotype; Humans; Kinases; Ligands; Male; Mortality; Pathogenesis; Physiological aspects; Polymorphism, Genetic - genetics; Proteins; Receptor for Advanced Glycation End Products - genetics; Risk Factors; Smoking; Ultrasonic imaging; Vascular surgery
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2015/394126

Accumulating evidence has suggested that receptor for advanced glycation end products (RAGE) is involved in the development and progression of human abdominal aortic aneurysms (AAAs). However, the association between RAGE gene polymorphisms and AAA has not yet been determined. The present study was aimed at analyzing the potential association between the RAGE gene polymorphisms and AAAs. A cohort of 381 patients and 436 age-matched healthy controls were genotyped to detect the three RAGE polymorphisms (−374 T/A, −429 T/C, and G82S) using SNaPshot. Our study demonstrated a significant difference in the genotype and allele frequencies of the RAGE G82S polymorphism between the AAA patients and the controls. Further stratification by gender and smoking status revealed that the presence of the RAGE 82S allele confers a higher risk for developing AAA in men and smokers. Moreover, AAA patients with the variant 82S allele of RAGE presented with reduced serum soluble RAGE (sRAGE) production, and this decrease was more significant in men and smokers with AAA. Our study provides preliminary evidence that the 82S allele of RAGE is a risk factor for AAA. This new piece of knowledge regarding RAGE may be clinically important for the prevention and therapy of AAAs.