M235T polymorphism in the AGT gene and A/GI8-83 substitution in the REN gene correlate with end-stage renal disease

Sarkar, S. ; Gupta, V. ; Kumar, A. ; Chaudhary, M. ; Diyundi, S. ; Sehajpal, P. K. ; Thangaraj, K. ; Rajender, S. (2015) M235T polymorphism in the AGT gene and A/GI8-83 substitution in the REN gene correlate with end-stage renal disease Nephron, 129 (2). pp. 104-108. ISSN 1660-8151

Full text not available from this repository.

Official URL: https://www.karger.com/Article/Abstract/370074

Related URL: http://dx.doi.org/10.1159/000370074

Abstract

Background/Aims: This study aimed at investigating if M235T polymorphism in the AGT gene and A/GI8-83 polymorphism in the REN gene correlate with End-stage Renal Disease (ESRD). Methods: We analyzed 173 ESRD patients and 329 individuals with normal kidney function for differences in the genotype distribution of AGT-M235T and REN- A/GI8-83polymorphisms between the two groups. The data for cases and controls were compared using the χ2 test. Results: We found significantly higher levels of serum creatinine and CRP in cases in comparison to controls (p < 0.0001). Data comparison showed a significant association of AGT M235T substitution with ESRD in the dominant model (p = 0.008) and in the comparison of the heterozygous substitution with the homozygous common genotype (p = 0.005). Similarly, REN A/GI8-83 polymorphism showed a significant difference in the distribution of genotypes between cases and controls (p < 0.038) such that a heterozygous substitution was significantly more common in the ESRD cases in comparison to the homozygous common genotype (p = 0.023). Conclusion: We conclude that heterozygous substitutions at the AGT M235T and REN A/GI8-83 loci correlate significantly with ESRD in a north Indian population.

Item Type:Article
Source:Copyright of this article belongs to Karger Publishers.
ID Code:107823
Deposited On:03 Jul 2017 05:46
Last Modified:03 Jul 2017 05:46

Repository Staff Only: item control page