Association of AGTR1 gene methylation and its genetic variant in Chinese farmer with hypertension: A case-control study

Abstract

The objective was to determine the potential associations of the angiotensin II receptor type 1 (AGTR1) gene polymorphism, methylation, and lipid metabolism in Chinese farmers with hypertension. A case-control study was conducted in Wuzhi county of Henan province in China in 2013 to 2014. A total of 1034 local residents (35–74 years, 386 hypertensive cases, and 648 normotensive subjects) were enrolled in this study. Triglyceride (TG), total cholesterol (TC), high-density lipoprotein, and low-density lipoprotein were measured using automatic chemistry analyzer. The AGTR1 gene promoter methylation level was measured using quantitative methylation-specific polymerase chain reaction method. The single nucleotide polymorphism rs275653 was genotyped with TaqMan probe assay at an applied biosystems platform. The gender, body mass index (BMI), TG, TC, and family history of hypertension in the hypertension group were significantly higher than those in control group (P < .05). No significant difference was observed in the distribution of AGTR1 rs275653 polymorphism in the hypertension and controls (P > .05). The AGTR1 gene methylation in subjects carrying different genotypes was not significantly observed (P > .05). The logistic regression analysis found the AGTR1 gene methylation level was negative correlation with hypertension in the present study (odds ratio, 0.946, 95% confidence interval, 0.896–0.999) through adjusting for age, gender, BMI, education, smoking, alcohol drinking, fruit and vegetable intake, pickles intake, and family history of hypertension. The association of AGTR1 gene hypomethylation and essential hypertension was observed in Chinese farmers; no significant difference was observed in the distribution of AGTR1 rs275653 polymorphism.

Effect of Polymorphic Variants of Agt2r1 Gene on Hemodynamic Parameters in Premature Children

“…Результати одного з нещодавно проведених досліджень вказують на зв'язок варіантів AGT2R1 з формуванням серцевої недостатності [8]. Певні Актуальні проблеми сучасної медицини епігенетичні зміни даного гену підвищують ризик есенціальної артеріальної гіпертензії [9] Разом з тим, є повідомлення щодо позитивного впливу АА-варіанту генотипу на неврологічний статус при субарахноїдальних крововиливах [10]. За результатами дослідження, проведеного українськими вченими, було виявлено що С-алель пов'язана з гіршим перебігом SARS-CoV-2, підвищеною кисневою залежністю, ймовірно, внаслідок кардіоваскулярних порушень [11].…”