Key result
Unfavorable AGTR1 CC genotype is linked to ~15-point lower PCS scores in hypertension vs AA genotype.
Why the study?
Quality-of-life indicators are increasingly important in monitoring hypertension and assessing treatment effectiveness, with improving quality of life representing a key objective of medical intervention.
Do genetic polymorphisms in the AGTR1 and NOS3 genes reduce quality of life in patients with arterial hypertension?
Observational (n=116)
Randomly divided into two treatment groups
No
Do genetic polymorphisms in the AGTR1 and NOS3 genes reduce quality of life in patients with arterial hypertension?
Genetic polymorphisms associated with reduced nitric oxide bioavailability (NOS3 T786C) or enhanced angiotensin II receptor activity (AGTR1 A1166C) are linked to significantly poorer physical and mental quality of life in patients with arterial hypertension.
May support genotype-informed QoL assessment in arterial hypertension; hypothesis-generating and should not yet change practice.
Objective. Recently, multicomponent quality-of-life indicators have become increasingly important in monitoring the health status of patients with hypertension and evaluating the effectiveness of treatment. Improving patient quality of life is considered one of the key objectives of the medical intervention. Methods. To assess the quality of life of patients with, we used the standardized SF-36 (Short Form-36 Health Survey) questionnaire, which allows to explicitly examine the respondent physical and psycho-emotional status. Results. We analyzed the association between polymorphisms of endothelial nitric oxide (NO) synthase (eNOS) (NOS3, T786C) and angiotensin II receptor type 1 (AGTR1, A1166C) genes and quality of life. Patients with polymorphisms associated with lower intravascular pressure had lower baseline QoL scores, particularly on the “physical functioning” and “general health” scales (p<0.05). Patients with heterozygous or homozygous “unfavorable” genotypes (AGTR1_CC, NOS3_CC) have significantly lower total indicators of both physical and psycho-emotional health compared to patients with “better” genotypes (AA, TT) and the control group. Conclusion. Patients with polymorphisms that cause reduced bioavailability of NO or excessive activation of AGRT1 show a significant deterioration in quality of life on all key SF-36 scales. This indicates the significant role of genetic factors in shaping the subjective perception of health in patients with arterial hypertension.
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Pidruchna et al. (2026) conducted an observational in Arterial hypertension (n=116). AGTR1 (A1166C) and NOS3 (T786C) unfavorable CC genotypes vs. Favorable genotypes (AA, TT) and healthy controls was evaluated on Physical Component Summary (PCS) score on SF-36 for AGTR1 (p=<0.05). Patients with arterial hypertension and unfavorable AGTR1 CC genotypes had significantly lower Physical Component Summary scores (54.5 vs 69.4) compared to those with favorable AA genotypes.
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