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Renalase gene polymorphism in patients with hypertension and concomitant coronary heart disease
Xiaogang Li1, Weihong Jiang, Luhong Li
1Department of Cardiovascular Medicine, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, China.
Insights
Renalase gene variations, specifically allele A of rs2576178, may increase coronary heart disease (CHD) risk in hypertensive patients. Allele C of rs2296545 is linked to hypertension susceptibility.
Area of Science:
- Genetics and genomics
- Cardiovascular disease research
- Medical research
Background:
- Hypertension and coronary heart disease (CHD) are significant global health concerns.
- Genetic factors play a role in the development of these conditions.
- Investigating gene polymorphisms can offer insights into disease predisposition.
Purpose of the Study:
- To examine renalase gene single nucleotide polymorphisms (SNPs) in patients with hypertension and concomitant CHD.
- To assess the genetic risk for CHD in hypertensive individuals.
- To identify potential genetic markers for hypertension and CHD.
Main Methods:
- Screening of SNPs using NCBI and HapMap genome databases.
- Genotyping of 791 hypertensive and CHD patients, 802 hypertensive patients, and 812 healthy controls.
- Analysis of genotype frequencies, allele frequencies, linkage disequilibrium, and Hardy-Weinberg equilibrium using Haploview 4.2 software and logistic regression.
Main Results:
- Allele A of rs2576178 was significantly more frequent in hypertensive patients with CHD compared to hypertensive patients (p=0.001, OR=1.625).
- Allele C of rs2296545 was significantly more frequent in hypertensive patients than in healthy controls (P=0.009, OR=1.436).
Conclusions:
- Allele A of rs2576178 may predispose hypertensive patients to CHD, with the AA genotype indicating susceptibility.
- Allele C of rs2296545 may predispose individuals to hypertension, with the CC genotype indicating susceptibility.
Background/Aims:
This study aimed to investigate renalase gene polymorphism in patients with hypertension and concomitant coronary heart disease (CHD) and to evaluate the risk for CHD in hypertensive patients from the view of genetics.
Methods:
NCBI and HapMap genome database were employed to screen the Single nucleotide polymorphisms (SNP). These SNPs were detected in hypertensive and CHD patients (n=791), hypertensive patients (n=802) and healthy controls (n=812), and the genotypes were recorded. Haploview 4.2 software was used to determine the genotypes, allele frequency, haplotypes, linkage disequilibrium and Hardy-Weinberg (HWE) equilibrium, and odds ratio (OR) was calculated with non-conditioned logistic regression analysis.
Results:
The frequency of allele A of rs2576178 in patients with hypertensive and CHD was markedly higher than that in hypertensive patients (p=0.001, OR=1.625,95% CI 1.221-2.160). The frequency of allele C of rs2296545 in hypertensive patients was significantly higher than that in healthy controls (P=0.009, OR=1.436, 95% CI 1.095-1.883).
Conclusion:
The allele A of rs2576178 may be a predisposing factor of CHD in hypertensive patients, and hypertensive patients with AA genotype are susceptible to develop CHD. The allele C of rs2296545 may be a predisposing factor of hypertension and patients with CC genotype are susceptible to develop hypertension.
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