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子痫前期发病与 AGTR1 基因多态性的关系。

Relationship between onset of eclampsia and AGTR1 gene polymorphisms.

机构信息

Department of Obstetrics, Dongying District People's Hospital, Dongying, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Dec;24(24):12638-12644. doi: 10.26355/eurrev_202012_24160.

Abstract

OBJECTIVE

We aimed to study the correlations of angiotensin II receptor type 1 (AGTR1) gene polymorphisms with the occurrence and development of eclampsia.

PATIENTS AND METHODS

A total of 200 pregnant women with eclampsia admitted to our hospital from January 1, 2017 to September 30, 2019 were collected as observation group and 200 normal pregnant women during the same period were recruited in the control group. Genome sequencing was performed to detect the AGTR1 gene polymorphisms in the two groups. Expression level of AGTR1 in both groups was detected. The influences of AGTR1 on clinical data of pregnant women with eclampsia were analyzed.

RESULTS

There were no significant differences in age (p=0.545), height (p=0.738), weight (p=0.695) and hypertension (p=0.372) between observation group and control group. However, significant differences were found in the distributions of alleles at AGTR1 rs1799870 (p=0.002) and AGTR1 rs52936049 (p=0.047) between groups. The frequencies of T allele at rs1799870 and rs52936044 in observation group were higher than those in the control group. In addition, the distributions of AGTR1 gene genotypes at rs1799870 (p=0.012), rs144520513 (p=0.008) and rs529360494 (p p =0.036) in observation group differed from those in control group. Observation group had higher frequencies of TT genotype at rs1799870, GG genotype at rs144520513 and TG genotype at rs529360494 than those in control group. Besides, the frequency of CGG haplotype (p=0.008) of AGTR1 gene in observation group was notably lower than that in the control group, while the frequency of TGT haplotype (p=0.012) of AGTR1 gene in the former was remarkably higher than that in the latter. Moreover, the linkage disequilibrium between rs529360494 and rs144520513 of AGTR1 gene was relatively high (D'=0.623). AGTR1 gene polymorphism rs529360494 showed an evident relationship with the expression of AGTR1 gene, and the expression of AGTR1 in pregnant women with eclampsia who carried TG genotype was markedly reduced (p<0.05). Furthermore, AGTR1 gene polymorphism rs1799870 was associated with prothrombin time (PT) in pregnant women with eclampsia (p=0.046), and PT in those carrying genotype TC was shorter. Rs144520513 was related to the levels of triglyceride (TG) (p<0.001) and low-density lipoprotein (LDL) (p<0.001) in pregnant women with eclampsia, and TG and LDL levels were significantly lower.

CONCLUSIONS

AGTR1 gene polymorphisms are closely associated with the onset and progression of eclampsia.

摘要

目的

研究血管紧张素 II 受体 1(AGTR1)基因多态性与子痫发生发展的关系。

方法

选取 2017 年 1 月 1 日至 2019 年 9 月 30 日我院收治的 200 例子痫患者作为观察组,同期选取 200 例正常孕妇作为对照组。采用基因组测序方法检测两组的 AGTR1 基因多态性。检测两组 AGTR1 的表达水平。分析 AGTR1 对子痫患者临床资料的影响。

结果

观察组与对照组在年龄(p=0.545)、身高(p=0.738)、体重(p=0.695)和高血压(p=0.372)方面无显著差异。然而,两组在 AGTR1 rs1799870(p=0.002)和 AGTR1 rs52936049(p=0.047)等位基因分布上存在显著差异。观察组 rs1799870 位点 T 等位基因频率高于对照组。此外,观察组 AGTR1 基因 rs1799870(p=0.012)、rs144520513(p=0.008)和 rs529360494(p<0.001)的基因型分布与对照组存在差异。观察组 rs1799870 位点 TT 基因型、rs144520513 位点 GG 基因型和 rs529360494 位点 TG 基因型频率高于对照组。此外,观察组 AGTR1 基因 CGG 单倍型(p=0.008)频率明显低于对照组,而 TGT 单倍型(p=0.012)频率明显高于对照组。此外,AGTR1 基因 rs529360494 与 rs144520513 之间存在较高的连锁不平衡(D'=0.623)。AGTR1 基因多态性 rs529360494 与 AGTR1 基因的表达明显相关,子痫患者携带 TG 基因型时 AGTR1 基因的表达明显降低(p<0.05)。此外,AGTR1 基因多态性 rs1799870 与子痫患者的凝血酶原时间(PT)有关(p=0.046),携带 TC 基因型的患者 PT 较短。rs144520513 与子痫患者的甘油三酯(TG)(p<0.001)和低密度脂蛋白(LDL)(p<0.001)水平有关,TG 和 LDL 水平显著降低。

结论

AGTR1 基因多态性与子痫的发生发展密切相关。

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