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内皮素-1基因多态性及其血浆水平与高血压和冠状动脉粥样硬化的关联。

The association of endothelin-1 gene polymorphism and its plasma levels with hypertension and coronary atherosclerosis.

作者信息

Ebrahimi Nazanin, Asadikaram Gholamreza, Mohammadi Abbas, Jahani Yunes, Moridi Mina, Masoumi Mohammad

机构信息

Physiology Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran.

Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Arch Med Sci. 2019 Jul 22;17(3):613-620. doi: 10.5114/aoms.2019.86770. eCollection 2021.

Abstract

INTRODUCTION

Endothelin-1 (ET-1) is the most potent among all vasoconstrictors, and its association with cardiovascular diseases has been reported before. Our aim was to investigate the association of ET-1 plasma level and its gene polymorphisms ( and ) with hypertension and coronary atherosclerosis (CA).

MATERIAL AND METHODS

This study was carried out on 128 women and 132 men, who were divided into 4 groups: hypertensive without atherosclerosis (H+A-); hypertensive with atherosclerosis (H+A+); non-hypertensive with atherosclerosis (H-A+); and non-hypertensive without atherosclerosis (control group). Endothelin-1 plasma levels were measured by ELISA, and gene polymorphisms were detected by polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP) methods. Coronary artery diseases (CAD) were then defined based on angiography data.

RESULTS

The ET-1 plasma level was significantly higher in the H+A+ group in comparison with the other groups, especially H+A-. Comparing people with CA and those without it, the highest frequency level of the T allele of was found in people with CA. Significantly higher frequencies of the 3A allele were detected in hypertensive patients in comparison with non-hypertensive individuals, when analyzing .

CONCLUSIONS

Endothelin-1 plasma level shows a direct association with the risk of CA development. The T allele of can be regarded as a risk factor for CA development. The 3A allele of can be associated with the risk of hypertension; therefore, it can be concluded that ET-1 and its gene polymorphisms play an important role in CA development and hypertension observed in the south-eastern populations of Iran.

摘要

引言

内皮素 -1(ET-1)是所有血管收缩剂中作用最强的,此前已有报道其与心血管疾病有关。我们的目的是研究ET-1血浆水平及其基因多态性( 和 )与高血压和冠状动脉粥样硬化(CA)的关联。

材料与方法

本研究对128名女性和132名男性进行,他们被分为4组:无动脉粥样硬化的高血压患者(H+A-);有动脉粥样硬化的高血压患者(H+A+);有动脉粥样硬化的非高血压患者(H-A+);无动脉粥样硬化的非高血压患者(对照组)。采用酶联免疫吸附测定法(ELISA)测量ET-1血浆水平,通过聚合酶链反应 - 限制性片段长度多态性(PCR-RFLP)方法检测基因多态性。然后根据血管造影数据定义冠状动脉疾病(CAD)。

结果

与其他组相比,尤其是H+A-组,H+A+组的ET-1血浆水平显著更高。比较有CA和无CA的人群,发现有CA的人群中 基因T等位基因的频率水平最高。在分析 时,与非高血压个体相比,高血压患者中检测到3A等位基因的频率显著更高。

结论

ET-1血浆水平与CA发生风险呈直接关联。 基因的T等位基因可被视为CA发生的危险因素。 基因的3A等位基因可能与高血压风险相关;因此,可以得出结论,ET-1及其基因多态性在伊朗东南部人群中观察到的CA发生和高血压中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c60/8130481/73c2c4a8b1c6/AMS-17-3-91675-g001.jpg

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