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Non-dipping and arterial hypertension depend on clinical factors rather than on genetic variability of ACE and RGS2 genes in patients with type 1 diabetes

机译:1型糖尿病患者的非浸润性和动脉性高血压取决于临床因素而不取决于ACE和RGS2基因的遗传变异

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摘要

The aim of our study was to characterize the association of clinical and genetic risk factors such as: ACE genotype (rs17997552, rs1800764, rs4459609) and RGS2 (rs2746071) with the development of hypertension (HT) and non-dipping phenomenon in patients with type 1 diabetes mellitus (T1DM). A total of 238 adolescents and young adults with T1DM—103 females and 135 males, aged 8–30 years (mean 17.35 ± 5.2) with diabetes duration 1–26 years (mean 7.72 ± 6.2), with mean HbA1c (IFCC) 58 ± 15 mmol/mmol—were subjected to 24-h ambulatory blood pressure measurements (ABPM). The results of the ABPM were analyzed in association with the polymorphisms of ACE and RGS2 genes and clinical data of patients. HT was recognized in 65 (27 %) and non-dipping in 111 (46.63 %) patients. In the multivariate analysis of factors predisposing to HT, the variables that remained significant were the following: male sex (OR 1.62; 95 % CI 1.171–2.250), non-dipping (OR 1.40; 95 % CI 1.03–1.90) and total cholesterol level (OR 1.01; 95 % CI 1.005–1.021). The only factor influencing non-dipping was the duration of diabetes—OR 1.09 (95 % CI 1.04–1.14). The patients displaying non-dipping have a twice increased risk of development of HT (OR 2.17; 95 % CI 1.21–3.89). There was no association between disturbances of blood pressure (BP) and genotypes of ACE: rs17997552, rs1800764, rs4459609 and RGS2: rs2746071. Clinical rather than genetic risk factors seem to be connected with BP disturbances in young patients with T1DM. Although we have identified representative groups of HT versus non-HT and dipping versus non-dipping subjects, the effect of genetic predisposition to the development of higher BP is too weak to be statistically significant.Electronic supplementary materialThe online version of this article (doi:10.1007/s00592-014-0568-0) contains supplementary material, which is available to authorized users.
机译:我们研究的目的是描述临床和遗传风险因素,如:ACE基因型(rs17997552,rs1800764,rs4459609)和RGS2(rs2746071)与2型糖尿病患者高血压(HT)和非浸入现象的关系1个糖尿病(T1DM)。共有238名T1DM的青少年和青年人-103名女性和135名男性,年龄8至30岁(平均17.35±5.2),糖尿病病程为1至26岁(平均7.72±6.2),平均HbA1c(IFCC)58± 15 mmol / mmol-进行24小时动态血压测量(ABPM)。结合ACE和RGS2基因的多态性以及患者的临床资料分析了ABPM的结果。 HT被确认为65(27%),非浸润被确认为111(46.63%)患者。在诱发HT的因素的多变量分析中,仍然显着的变量如下:男性(OR 1.62; 95%CI 1.171–2.250),不浸洗(OR 1.40; 95%CI 1.03-1.90)和总胆固醇水平(OR 1.01; 95%CI 1.005–1.021)。影响非蘸药的唯一因素是糖尿病的持续时间-OR 1.09(95%CI 1.04-1.14)。表现出不蘸药的患者出现HT的风险增加了两倍(OR 2.17; 95%CI 1.21-3.89)。血压(BP)障碍与ACE基因型之间没有关联:rs17997552,rs1800764,rs4459609和RGS2:rs2746071。在年轻的T1DM患者中,临床而非遗传危险因素似乎与BP障碍有关。尽管我们已经确定了HT与非HT,浸入与非浸入受试者的代表性人群,但是遗传易感性对较高BP发生的影响太弱了,以至于没有统计学意义。电子补充材料本文的在线版本(doi: 10.1007 / s00592-014-0568-0)包含补充材料,授权用户可以使用。

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