Changes in lipid profile parameters depending on the a1166c polymorphism of the angiotensin II type I receptor gene as a predictor of arterial hypertension.

Q4 Medicine Wiadomosci lekarskie Pub Date : 2024-01-01 DOI:10.36740/WLek202408104
Volodymyr V Shmanko, Svitlana R Pidruchna, Roman V Hnizdyukh, Alla E Mudra, Uliana M Zakharchuk, Iryna P Kuzmak, Tetiana Y Yaroshenko, Lylya M Palytsya, Iryna A Bandas, Volodymyr H Dzhyvak, Iryna M Nikitina, Iryna F Zavarynska
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Abstract

Objective: Aim: To investigate lipid profile parameters depending the polymorphism of the A1166C I type gene receptor of the angiotensin II as a predictor of arterial hypertension.

Patients and methods: Materials and Methods: The study involved 86 patients with arterial hypertension. The control group consisted of 30 practically healthy individuals. Indicators of lipid metabolism in the blood serum of patients were determined using "Lachema" kits on an analyzer. The the polymorphism of the A1166C I type gene receptor of the angiotensin II was studied by polymerase chain reaction with electrophoretic detection of the results.

Results: Results: Higher levels of total cholesterol were found in patients with CC genotype compared to AA genotype carriers ((8.94±0.09) vs (5.18±0.02) mmol/L). The level of low-density lipoprotein in CC-genotype carriers was (7.43±0.03) versus (3.66±0.02) mmol/L in A-allele homozygotes. Triglycerides and very low density lipoproteins were also significantly higher in CC genotype carriers compared to patients with AA genotype. The level of high-density lipoprotein was lower in homozygotes with C-allele than in patients with the AA genotype, and was (0.59±0.12) versus (0.99±0.03) mmol/L.

Conclusion: Conclusions: The presence in the CC genotype the I type gene receptor of the angiotensin II type is a predictor of dyslipidemia. In patients with arterial hypertension, the presence in the C-allele of the I type gene of the angiotensin II type contributes to a significant increase in serum adipokines and a decrease in ghrelin levels.

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血管紧张素 II I 型受体基因 a1166c 多态性导致的血脂参数变化可预测动脉高血压。
目的目的:研究作为动脉高血压预测因子的血管紧张素 II 的 A1166C I 型基因受体多态性的血脂谱参数:材料与方法研究涉及 86 名动脉高血压患者。对照组由 30 名健康人组成。使用分析仪上的 "Lachema "试剂盒测定患者血清中的脂质代谢指标。通过聚合酶链式反应研究了血管紧张素 II 受体 A1166C I 型基因的多态性,并对结果进行了电泳检测:结果:结果:与 AA 基因型携带者相比,CC 基因型患者的总胆固醇水平更高((8.94±0.09) mmol/L vs (5.18±0.02) mmol/L)。CC基因型携带者的低密度脂蛋白水平为(7.43±0.03)毫摩尔/升,而A基因型等位基因携带者为(3.66±0.02)毫摩尔/升。CC 基因型携带者的甘油三酯和极低密度脂蛋白也明显高于 AA 基因型患者。与 AA 基因型患者相比,C-等位基因同型患者的高密度脂蛋白水平较低,为(0.59±0.12)毫摩尔/升对(0.99±0.03)毫摩尔/升:结论血管紧张素 II I 型基因受体的 CC 基因型是血脂异常的预测因子。在动脉高血压患者中,血管紧张素 II I 型基因 C-等位基因的存在会导致血清脂肪因子显著增加,胃泌素水平下降。
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来源期刊
Wiadomosci lekarskie
Wiadomosci lekarskie Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
482
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