Key result
ACE rs4362 TT genotype linked to ~17-fold higher risk of CKD advancement in ADPKD.
Why the study?
Does the ACE gene rs4362 polymorphism influence the progression of kidney failure in patients with autosomal dominant polycystic kidney disease?
Case-Control (n=208)
No
Does the ACE gene rs4362 polymorphism influence the progression of kidney failure in patients with autosomal dominant polycystic kidney disease?
Odds Ratio: 17.04 (95% CI 2.38–121.95)
p-value: p=0.005
The ACE gene rs4362 TT genotype is associated with an increased risk of advanced chronic kidney disease in patients with ADPKD, acting as an effect modifier for hypertension.
BACKGROUND & OBJECTIVES: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited systemic disorder, characterized by the fluid filled cysts in the kidneys leading to end stage renal failure in later years of life. Hypertension is one of the major factors independently contributing to the chronic kidney disease (CKD) progression. The renin-angiotensin aldosterone system (RAAS) genes have been extensively studied as hypertension candidate genes. The aim of the present study was to investigate the role of angiotensin converting enzyme tagging - single nucleotide polymorphisms (ACE tag-SNPs) in progression of CKD in patients with ADPKD. m0 ethods: In the present study six ACE tagSNPs (angiotensin converting enzyme tag single nucleotide polymorphisms) and insertion/deletion (I/D) in 102 ADPKD patients and 106 control subjects were investigated. The tagSNPs were genotyped using FRET-based KASPar method and ACE ID by polymerase chain reaction (PCR) and electrophoresis. Genotypes and haplotypes were compared between ADPKD patients and controls. Univariate and multivariate logistic regression analyses were performed to assess the effect of genotypes and hypertension on CKD advancement. Mantel-Haenszel (M-H) stratified analysis was performed to study the relationship between different CKD stages and hypertension and their interaction. RESULTS: All loci were polymorphic and except rs4293 SNP the remaining loci followed Hardy-Weinberg equilibrium. Distribution of ACE genotypes and haplotypes in controls and ADPKD patients was not significant. A significant linkage disequilibrium (LD) was observed between SNPs forming two LD blocks. The univariate analysis revealed that the age, hypertension, family history of diabetes and ACE rs4362 contributed to the advancement of CKD. INTERPRETATION & CONCLUSIONS: The results suggest that the ACE genotypes are effect modifiers of the relationship between hypertension and CKD advancement among the ADPKD patients.
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Ramanathan et al. (2016) conducted a case-control in Autosomal dominant polycystic kidney disease (ADPKD) (n=208). ACE gene rs4362 polymorphism (TT genotype) vs. CC genotype was evaluated on Advancement of chronic kidney disease (advanced vs early stage) (OR 17.04, 95% CI 2.38-121.95, p=0.005). The TT genotype of the ACE rs4362 polymorphism significantly increased the risk of chronic kidney disease advancement in patients with autosomal dominant polycystic kidney disease (OR 17.04).
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