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Published on: October 26, 2020
Association between AGTR1 (c.1166 A>C) Polymorphisms and Kidney Injury in Hypertension
Yiyao Zeng1,2, Yufeng Jiang1,2, Ziyin Huang1,2
1Department of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Medical Center of Soochow University, Suzhou Dushu Lake Hospital, 215000 Suzhou, Jiangsu, China.
Insights
This study found a link between the AGTR1 gene (c.1166 A>C) polymorphism and hypertension with kidney damage. Understanding these genetic variations may aid in precision gene therapy for hypertension.
Area of Science:
- Genetics
- Cardiology
- Nephrology
Background:
- High blood pressure is a leading cause of cardiovascular diseases.
- Kidney damage is a common secondary complication of hypertension.
- Investigating hypertension gene polymorphisms is crucial for precision treatment.
Purpose of the Study:
- To explore the association between AGTR1 (c.1166 A>C) gene polymorphisms and hypertension with kidney damage.
- To examine different genetic models (codominant, dominant, recessive) and their relation to hypertension and kidney injury.
- To assess the susceptibility of various genotypes to hypertension with kidney injury.
Main Methods:
- The study involved 292 hypertensive patients and 44 with hypertension and kidney injury.
- AGTR1 polymorphism distribution was analyzed using the PCR-melting curve method.
- Genotype distributions were compared between groups.
Main Results:
- Genotype distributions in hypertension and combined groups adhered to Hardy-Weinberg equilibrium (p > 0.05).
- Statistically significant differences were observed in the distribution of three genotypes (p < 0.05).
- Codominant, dominant, and recessive genotype frequencies showed significant differences (p < 0.05), with no significant difference between A and C alleles (p > 0.05).
Conclusions:
- The AGTR1 (c.1166 A>C) polymorphism is associated with hypertension combined with renal injury.
- Comparison of different genetic models provides insights into susceptibility.
- Findings may offer new targets for precision gene therapy in hypertension management.
Background:
High blood pressure is the main cause of cardiovascular diseases. Kidney damage is one of the most common organ secondary damage to hypertension. The study of hypertension gene polymorphisms is an important means of precision treatment of primary hypertension.
Objectives:
The objective of this study was to explore the relationship between AGTR1 (c.1166 A>C) gene polymorphisms and hypertension combined with kidney damage, while exploring the relationship between codominant, dominant and recessive gene model and hypertension with kidney injury and the susceptibility of different genotypes to hypertension with kidney injury.
Methods:
The distribution of AGTR1 polymorphism in the AGTR1 in hypertensive patients (hypertension group, 292 patients) and hypertension with kidney injury patients (44 patients) were detected and compared by PCR-melting curve method.
Results:
The genotype distribution of hypertension and combined groups met Hardy-Weinberg equilibrium (p > 0.05); the distribution difference between the three genotypes was statistically significant (p < 0.05), the codominant, dominant and recessive distribution frequency of genotypes (p < 0.05), and no difference between A allele and C allele (p > 0.05).
Conclusions:
Our study identified the relationship of AGTRA (c.1166 A>C) with hypertension combined with renal injury, and compared the susceptibility of different genetic models, which may provide novel targets for precision gene therapy of hypertension.
Clinical Trial Registration:
URL: https://www.chictr.org.cn/indexEN.html; Unique identifier: ChiCTR2100051472.
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