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血清血管紧张素II、激肽释放酶1水平及血管紧张素转换酶/激肽释放酶1基因多态性与冠状动脉狭窄所致急性心肌梗死的相关性

Association of serum levels of AngII, KLK1, and ACE/KLK1 polymorphisms with acute myocardial infarction induced by coronary artery stenosis.

作者信息

Dai Shu-hong, Li Ji-fu, Feng Jin-bo, Li Rui-jian, Li Chuan-bao, Li Zhuo, Zhang Yun, Li Da-qing

机构信息

The Key Laboratory of Cardiovascular Remodelling and Function Research, Chinese Ministry of Education and Chinese Ministry of Health, China Department of cardiology, Qilu Hospital, Shandong University, China.

Department of obstetrics and gynecology, Qilu Hospital, Shandong University, China.

出版信息

J Renin Angiotensin Aldosterone Syst. 2016 Jun 21;17(2):1470320316655037. doi: 10.1177/1470320316655037. Print 2016 Apr-Jun.

DOI:10.1177/1470320316655037
PMID:27329205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5843928/
Abstract

INTRODUCTION

The study aims to confirm the association of acute myocardial infarction (AMI) with serum angiotensin II (AngII), kallikrein1 (KLK1), and ACE/KLK1 polymorphisms.

MATERIALS AND METHODS

Serum AngII/KLK1 levels and ACE and KLK1 genotypes were determined in 208 patients with AMI and 216 normal controls. Binary logistic regression was used for data analysis.

RESULTS

The differences in serum AngII levels were statistically significant between the groups. After adjusting for potential confounding factors, high serum levels of AngII and KLK1 significantly increased the risk of AMI. The individuals with ACE DD and KLK1 GG genotypes significantly increased the risk of AMI compared with those harboring the ACE II and KLK1 AA genotypes (OR = 8.77, 95% CI = 1.74-44.16).

CONCLUSIONS

(1) Increasing the serum levels of AngII increased the risk of AMI. (2) The risk of AMI increased significantly when the serum levels of AngII and KLK1 simultaneously increased. (3) Individuals with the combined genotypes of ACE DD and KLK1 GG showed significantly increased risk of AMI compared with those with the combined genotypes of ACE II and KLK1 AA.

摘要

引言

本研究旨在证实急性心肌梗死(AMI)与血清血管紧张素II(AngII)、激肽释放酶1(KLK1)以及ACE/KLK1基因多态性之间的关联。

材料与方法

测定了208例急性心肌梗死患者和216例正常对照者的血清AngII/KLK1水平以及ACE和KLK1基因型。采用二元逻辑回归进行数据分析。

结果

两组之间血清AngII水平差异具有统计学意义。在调整潜在混杂因素后,血清AngII和KLK1水平升高显著增加了急性心肌梗死的风险。与携带ACE II和KLK1 AA基因型的个体相比,携带ACE DD和KLK1 GG基因型的个体急性心肌梗死风险显著增加(OR = 8.77,95% CI = 1.74 - 44.16)。

结论

(1)血清AngII水平升高增加了急性心肌梗死的风险。(2)当血清AngII和KLK1水平同时升高时,急性心肌梗死风险显著增加。(3)与携带ACE II和KLK1 AA联合基因型的个体相比,携带ACE DD和KLK1 GG联合基因型的个体急性心肌梗死风险显著增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6729/5843928/ebc4e1feea2d/10.1177_1470320316655037-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6729/5843928/64337aef21bd/10.1177_1470320316655037-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6729/5843928/ebc4e1feea2d/10.1177_1470320316655037-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6729/5843928/64337aef21bd/10.1177_1470320316655037-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6729/5843928/ebc4e1feea2d/10.1177_1470320316655037-fig2.jpg

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1
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2
20-HETE Activates the Transcription of Angiotensin-Converting Enzyme via Nuclear Factor-κB Translocation and Promoter Binding.20-羟基二十碳四烯酸通过核因子-κB易位和启动子结合激活血管紧张素转换酶的转录。
J Pharmacol Exp Ther. 2016 Mar;356(3):525-33. doi: 10.1124/jpet.115.229377. Epub 2015 Dec 23.
3
Dual regulation of transcription factor Nrf2 by Keap1 and by the combined actions of β-TrCP and GSK-3.
Genes (Basel). 2021 Oct 1;12(10):1572. doi: 10.3390/genes12101572.
4
Influence of ACE Gene I/D Polymorphism on Cardiometabolic Risk, Maximal Fat Oxidation, Cardiorespiratory Fitness, Diet and Physical Activity in Young Adults.ACE 基因 I/D 多态性对年轻成年人的心脏代谢风险、最大脂肪氧化、心肺功能适应性、饮食和体力活动的影响。
Int J Environ Res Public Health. 2021 Mar 26;18(7):3443. doi: 10.3390/ijerph18073443.
5
Role of Angiotensin-Converting Enzyme (ACE) gene polymorphism and ACE activity in predicting outcome after acute myocardial infarction.血管紧张素转换酶(ACE)基因多态性及ACE活性在预测急性心肌梗死后预后中的作用
Int J Cardiol Heart Vasc. 2021 Jan 1;32:100701. doi: 10.1016/j.ijcha.2020.100701. eCollection 2021 Feb.
6
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7
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8
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