Federal State Budgetary Institution "Research Institute for Complex Issues of Cardiovascular Diseases", 6, Sosnoviy Blvd, 650002, Kemerovo, Russia.
BMC Cardiovasc Disord. 2020 Apr 15;20(1):169. doi: 10.1186/s12872-020-01464-7.
To study the genetic forms and pathophysiology of arterial hypertension by evaluating plasma renin activity in the Shors, minor indigenous peoples inhabiting the south of Western Siberia.
A single-stage study of indigenous (the Shors) and non-indigenous peoples living in the villages of Gornaya Shoria of the Kemerovo region in the south of Western Siberia was conducted in the period from 2013 to 2017. One thousand four hundred nine adults (901 Shors and 508 non-indigenous inhabitants) were recruited in the study using a continuous sampling plan. Arterial blood pressure was measured according to 2018 ESC/ESH guidelines for the management of arterial hypertension. All the respondents underwent clinical and instrumental examination. Plasma renin activity was determined by enzyme-linked immunoassay with the BRG kits (Germany). Polymorphisms of ACE (I/D, rs 4340), АGT (c.803 T > C, rs699), AGTR1 (А1166С, rs5186), ADRB1 (с.145A > G, Ser49Gly, rs1801252) and ADRA2B (I/D, rs 28,365,031) genes were tested using polymerase chain reaction.
Renin-dependent hypertensive patients prevailed in both ethnic groups (65.6% in the indigenous group vs. 89.8% in the non-indigenous group, p = 0.001). Prevalence of a volume-dependent AH was low in both groups (34.4% in the indigenous group vs. 10.2% in the non-indigenous group, р = 0.001). The D/D and Т/Т genotypes of the АСЕ [OR = 6.97; 95% CI (1.07-55.58)] and AGT [OR = 3.53; 95% CI (1.02-12.91)] genes were associated with the renin-dependent AH in the Shors. The C/C genotype of AGTR1 gene was found to predispose to the volume-dependent AH [OR = 5.25; 95% CI (1.03-27.89)]. The C/C genotype of AGTR1 gene was associated with moderate or high renin levels suggesting essential AH in the non-indigenous group [OR = 5.00; 95% CI (1.21-22.30), р = 0.029].
An in-depth understanding of AH pathophysiology and its genetic forms ensures the optimal choice of blood pressure-lowering treatment and optimizes AH control.
通过评估居住在西西伯利亚南部戈尔纳亚绍里亚村的少数民族(绍尔人)的血浆肾素活性,研究动脉高血压的遗传形式和病理生理学。
在 2013 年至 2017 年期间,对居住在西西伯利亚南部克麦罗沃地区戈尔纳亚绍里亚村的原住民(绍尔人)和非原住民进行了一项单阶段研究。使用连续抽样计划,招募了 1409 名成年人(901 名绍尔人和 508 名非原住民居民)。根据 2018 年 ESC/ESH 动脉高血压管理指南测量动脉血压。所有受访者均接受临床和仪器检查。采用 BRG 试剂盒(德国)通过酶联免疫吸附试验测定血浆肾素活性。使用聚合酶链反应检测 ACE(I/D,rs4340)、AGT(c.803T> C,rs699)、AGTR1(A1166C,rs5186)、ADRB1(c.145A>G,Ser49Gly,rs1801252)和 ADRA2B(I/D,rs28,365,031)基因的多态性。
在两个族群中,依赖肾素的高血压患者均占优势(原住民组为 65.6%,非原住民组为 89.8%,p=0.001)。两个族群中容量依赖性 AH 的患病率均较低(原住民组为 34.4%,非原住民组为 10.2%,p=0.001)。在绍尔人中,ACE [OR=6.97;95%CI(1.07-55.58)]和 AGT [OR=3.53;95%CI(1.02-12.91)]基因的 D/D 和 T/T 基因型与依赖肾素的 AH 相关。AGTR1 基因的 C/C 基因型被发现易患容量依赖性 AH [OR=5.25;95%CI(1.03-27.89)]。非原住民组中,AGTR1 基因的 C/C 基因型与中重度肾素水平相关,提示存在原发性高血压 [OR=5.00;95%CI(1.21-22.30),p=0.029]。
深入了解 AH 的病理生理学及其遗传形式可确保降压治疗的最佳选择,并优化 AH 的控制。