Key result
AGT rs699 polymorphism shows no association with blood pressure or RAAS parameters in Black South Africans.
Why the study?
The pathogenesis of hypertension remains incompletely understood, and the AGT rs699 (M235T) variant may influence blood pressure via the renin-angiotensin-aldosterone system. The relationships between rs699 genotypes, RAAS parameters, blood pressure, BMI, and gender in a black elderly population required evaluation.
Does the AGT rs699 (M235T) genetic variant influence renin–angiotensin–aldosterone system parameters (ACE, Ang I, Ang II), blood pressure, or body mass index in a predominantly hypertensive elderly Black South African cohort?
Cross-Sectional (n=48)
No
Does the AGT rs699 (M235T) genetic variant influence renin–angiotensin–aldosterone system parameters (ACE, Ang I, Ang II), blood pressure, or body mass index in a predominantly hypertensive elderly Black South African cohort?
In this small hypothesis-generating cohort of elderly Black South Africans, the AGT M235T (rs699) variant was predominantly present as the GG genotype (93.8%) and showed no statistically significant association with circulating RAAS parameters, blood pressure, or BMI.
Answers are grounded in this paper and cite their sources.
No association in this small elderly cohort; leaves open rs699 relevance to BP or RAAS in broader Black African populations.
Background Hypertension (HTN) is a key cardiovascular risk factor, with its pathogenesis remaining incompletely understood. Blood pressure (BP) regulation involves the Renin–Angiotensin–Aldosterone System (RAAS), including the Angiotensin-converting enzyme (ACE), Angiotensin I (Ang I) and Angiotensin II (Ang II). The rs699 variant (M235T) may influence BP via the RAAS. Aim This study aimed to evaluate the relationships between the rs699 genotypes, RAAS parameters, BP, Body mass index (BMI) and gender in a black elderly population. Methods Data were collected from 48 participants aged ≥60 years, using World Health Organization (WHO) obesity guidelines and South African Hypertension Society (SAHS) 2019 standards for HTN categories. Statistical analysis was performed using IBM SPSS version 27 and Python 3.14. Results Most participants possessed the rs699 variant (GG: 93.8%, AG: 4.2%). ACE levels were low in 64.6%, while Ang II was elevated in the same percentage. The majority were classified as hypertensive and obese. No significant associations were found between the rs699 variant and ACE, Ang I, Ang II, HTN, BMI or gender, though BMI showed sex-related differences in females. Conclusion Our findings suggest no significant association of the rs699 variant on RAAS or cardiometabolic parameters within the study population, warranting cautious interpretation. These findings require validation in larger and more diverse populations, as meaningful statistical inferences cannot be drawn from the current data.
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Grobler et al. (2026) conducted a cross-sectional in Hypertension (n=48). AGT rs699 (M235T) polymorphism vs. Alternative rs699 genotypes was evaluated on Association of AGT rs699 SNP with blood pressure (BP) (OR 0.9895, 95% CI 0.9299 – 1.0529, p=0.7384). The AGT rs699 (M235T) polymorphism was not significantly associated with blood pressure (OR 0.9895, p=0.7384) or RAAS parameters in elderly Black South Africans.
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