A single nucleotide polymorphism in the SLC19A1 gene is associate | 54331
Clinical & Experimental Cardiology

Clinical & Experimental Cardiology
Open Access

ISSN: 2155-9880

+44 1300 500008

A single nucleotide polymorphism in the SLC19A1 gene is associated with thoracic aortic aneurysms and dissection in Indian Population

Global Summit on Heart Diseases and Therapeutics

October 20-21, 2016 Chicago, USA

Kalpnath, Sujatha Sunil, Priya Jagia, S K Choudhary, R K Bhatnagar and Sanjiv Sharma

All India Institute of Medical Sciences, India
International Centre for Genetic Engineering and Biotechnology, India

Posters & Accepted Abstracts: J Clin Exp Cardiolog

Abstract :

Objective: Genetic susceptibility is an important risk factor for aortic wall degeneration and its leads to thoracic aortic aneurysm and dissection (TAAD). In many patients with TAD, the aorta progressively dilates and ultimately ruptures. The purpose of this study was to determine the single nucleotide polymorphism in 6 genes associated with thoracic aortic aneurysm and dissection patients in Indian population-A case-control study. Methods: Genomic DNA was isolated from blood and aortic wall tissue of 66 patients with degenerative TAAD, and 67 control individuals. Six SNPs: rs819146, rs8003379, rs2853523, rs326118, rs3788205, and rs10757278 were genotyped using TaqMan SNP genotyping assays (Applied Biosystems, Foster City, USA). The data were analyzed using STATA11.0 statistical software. Associations between polymorphisms and disease in tissue, blood and within gender were estimated with odds ratios and their 95% confidence intervals. Results: The T allele frequency for the SNP on 21q22.3, 5��? near gene as rs3788205 (-2174 C/T) was higher in male patients than in male controls (P-0.049). Moreover, with adjustment for traditional cardiovascular risk factors (sex, age, hypertension dyslipidemia diabetes and smoking), the rs3788205 {odd ratio (OD) 0.41, 95% confidence interval (CL) 0.14 to 1.09} polymorphism was found to be an independent susceptibility factor for TAAD in males. Conclusion: Our results suggest that a sequence variant on 21q22.3 is an important susceptibility locus that confers high cross-race risk for development of TAAD in Indian population.

Biography :