Why the study?
Valsartan exhibits noticeable interindividual variation in response among hypertensive patients, and the study aimed to explore this variation considering the functional AGT M235T variant and nongenetic factors.
Does the AGT M235T genotype influence the blood pressure response to valsartan in patients with essential hypertension?
Does the AGT M235T genotype influence the blood pressure response to valsartan in patients with essential hypertension?
The AGT M235T genotype, along with age, height, and sex, significantly influences the blood pressure-lowering response to valsartan, highlighting potential avenues for personalized hypertension management.
AGT M235T may explain valsartan response variability in hypertension; leaves open utility for guiding therapy pending validation.
Background Valsartan, an angiotensin receptor antagonist widely used in hypertension and heart failure management, exhibits noticeable interindividual variation in response among hypertensive patients at the University of Jordan Hospital. The angiotensinogen (AGT) gene variant M235T, a functional genetic variant, influences the renin‐angiotensin system. Aims This study aims to explore interindividual variations in the valsartan response, considering genetics, particularly the AGT M235T variant, and other nongenetic factors. Methods This cohort study involved 95 unrelated Arabic Jordanians diagnosed with essential hypertension. Systolic (SBP) and diastolic blood pressure (DBP) measurements were taken at the initiation of 160 mg valsartan and after 1 month of treatment, assessing the valsartan response for each patient. Genetic analysis of AGT M235T was done using the polymerase chain reaction‐restriction fragment length polymorphism genotyping method. Anthropometric data were collected from University of Jordan Hospital computer records. Results Valsartan response assessment revealed diverse individual responses, the response to valsartan varied, with SBP reductions from < 10 to > 70 mmHg and DBP from < 2 to 30 mmHg. Patients with homozygous AGT M235T genotypes showed a less significant response (p < 0.05) to valsartan than heterozygous and reference genotypes. Additionally, results indicated a positive correlation of age (p = 0.03) and a negative correlation of height (p = 0.02–0.04) with the valsartan response. Regression analysis demonstrated that the patients' sex significantly influenced the valsartan response (p < 0.05). Conclusions This study identifies the AGT M235T genotype as a potential genetic contributor to variability in the valsartan response. Associations with age, height, and sex underscore the importance of considering genetic and demographic factors in tailoring valsartan therapy, for advancing personalized hypertension management.
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Alhawari et al. (2025) studied this question.
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