BOGOMOLETS NATIONAL MEDICAL UNIVERSITY, KYIV, UKRAINE.
KHARKIV MEDICAL ACADEMY OF POSTGRADUATE EDUCATION, KHARKIV, UKRAINE.
Wiad Lek. 2022;75(2):533-540.
The aim: Objective of the research is to determine the effect of NOS3 and AGTR1 genotypes of patients with arterial hypertension and high body mass index in the course of the disease.
Materials and methods: 58 patients (22 men and 36 women) with AH and high BMI were examined. The average age of the examined patients was 53.6±8.7 years. The analysis of rs1799983 polymorphisms of the NOS3 gene (localization 7q36.1; 7:150999023) and AGTR1 (type 1 receptor for angiotensin 2 1166 A>C) was performed using TaqMan assay (Thermo Fisher Scientific, USA) by real-time PCR (Applied Biosystems, USA) using TaqMan probe amplification products. Genomic DNA samples were isolated from stabilized blood using a Genomic DNA Mini Kit reagent (Invitrogen, USA). The Statistica 10 program (StatSoft Inc.) was used for statistical processing of the obtained data, USA). The independent samples were compared using the Mann-Whitney (U) criterion. In all cases of statistical evaluation, the reliability of differences was taken into account at a value of p<0.05.
Results and conclusions: Polymorphism of the NOS3 and AGTR1 genes is associated with early development and complicated course of cardiovascular pathology. The combination of NOS3 and AGTR1 gene polymorphism in patients with the high body mass index increases the risk of complications in hypertension. Using a mathematical model to predict the probability (95%) of genetic mutations in two genes (NOS3 and AGTR1) increases the effectiveness of diagnosis for patients with the high risk of developing cardiovascular complications.
本研究旨在确定 NOS3 和 AGTR1 基因型对患有动脉高血压和高身体质量指数的患者在疾病过程中的影响。
对 58 名(22 名男性和 36 名女性)患有高血压和高 BMI 的患者进行了检查。被检查患者的平均年龄为 53.6±8.7 岁。NOS3 基因(位于 7q36.1;7:150999023)rs1799983 多态性和 AGTR1(血管紧张素 2 1 型受体)的分析采用 TaqMan 检测法(Thermo Fisher Scientific,美国)通过实时 PCR(Applied Biosystems,美国)使用 TaqMan 探针扩增产物进行。使用 Genomic DNA Mini Kit 试剂(Invitrogen,美国)从稳定的血液中分离基因组 DNA 样本。使用 Statistica 10 程序(StatSoft Inc.,美国)对获得的数据进行统计处理。使用 Mann-Whitney(U)标准比较独立样本。在所有统计评估的情况下,都考虑了差异的可靠性,其值为 p<0.05。
结果和结论:NOS3 和 AGTR1 基因的多态性与心血管病理学的早期发展和复杂病程有关。高身体质量指数患者的 NOS3 和 AGTR1 基因多态性组合增加了高血压并发症的风险。使用数学模型预测两个基因(NOS3 和 AGTR1)的基因突变概率(95%)可提高患有心血管并发症高危患者的诊断效果。