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Association of Angiotensin II Type 1 Receptor (AT1R) Gene Polymorphism with Angiotensin II Serum Levels in Patients
M Prasad1, D Rajarajeswari1, K Ramlingam1
1Department of Biochemistry, Narayana Medical College and Hospital, Chinthareddy Palem, Nellore, Andhra Pradesh 524003 India.
Insights
Essential hypertension (EH) risk is linked to the AT1R gene
Area of Science:
- Cardiovascular Genetics
- Molecular Medicine
- Hypertension Research
Background:
- Essential hypertension (EH) is a complex, polygenic condition with significant morbidity and mortality.
- EH contributes to severe comorbidities like stroke, myocardial infarction, cardiac, and renal failure.
- There is a need for population-based studies to understand EH pathophysiology and improve diagnosis and treatment.
Purpose of the Study:
- To investigate the genotype and allele frequencies of the AT1R gene A1166C polymorphism in Indian patients with EH.
- To correlate these genetic variations with serum Angiotensin II levels in hypertensive individuals.
- To assess the association between AT1R gene polymorphism and the risk of developing essential hypertension in the Indian population.
Main Methods:
- A case-control study involving 200 Indian patients with EH and 200 age- and gender-matched controls.
- Genotyping of the AT1R gene A1166C polymorphism was performed.
- Serum Angiotensin II levels were measured and correlated with genotypes.
Main Results:
- The C/A heterozygote and allele C of the AT1R gene A1166C polymorphism were significantly associated with an increased risk of EH in both men and women.
- Patients with EH exhibited higher serum Angiotensin II levels, particularly those with C/A and AA genotypes.
- A significant association was found between the 1166 C/A polymorphism of the AT1R gene and an elevated risk of hypertension in the Indian population.
Conclusions:
- The 1166 C/A polymorphism in the AT1R gene is a significant genetic risk factor for essential hypertension in the Indian population.
- This polymorphism is associated with elevated serum Angiotensin II levels, suggesting a mechanistic link to hypertension.
- These findings contribute to understanding the genetic underpinnings of EH and may inform future diagnostic or therapeutic strategies.
Abstract:
Essential hypertension (EH) is a multifactorial, polygenic condition, and is one of the most important comorbidities that contributes to stroke, myocardial infarction, cardiac failure, and renal failure. The continuous increasing rate of morbidity and mortality associated with EH presents an unmet need of population-based studies to explore pathophysiology as well as newer strategies for better diagnosis, prognosis and treatment. This study aimed to determine genotype and allele frequencies of A1166C polymorphism of AT1R gene in Indian patients with EH and correlated with serum levels of Angiotensin II. A total of 200 patients with EH and 200 age- and gender-matched control individuals were included in this study from the General Medicine Department Outpatient at Narayana Medical College and Hospital, Nellore, Andhra Pradesh, India. Patients with systolic blood pressure (SBP) ≥ 140 mmHg and/or diastolic blood pressure (DBP) ≥ 90 mmHg were considered as hypertensive. The findings of this study revealed significantly increased risk of C/A heterozygote and allele C in both men and women. Moreover, both men and women patients with EH showed higher serum levels of Angiotensin II with C/A as well as AA genotypes. These findings indicate a significant association of 1166 C/A polymorphism of the AT1R gene with increased risk of hypertension in Indian population.
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