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NOS3AS 变体对原发性高血压易感性的影响:伊朗西部克尔曼沙阿省的一项研究。

Contribution of NOS3AS Variants to Susceptibility to Essential Hypertension: A Study in Kermanshah Province, Western Iran.

机构信息

Department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Medical Genetics Laboratory, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Biochem Genet. 2023 Oct;61(5):2149-2158. doi: 10.1007/s10528-023-10364-2. Epub 2023 Mar 26.

DOI:10.1007/s10528-023-10364-2
PMID:36966459
Abstract

Hypertension (HTN) is a global health challenge and increase the risk of cardiovascular disease. Hypertension has a multifactorial course of evolution, with both genetic and environmental factors playing an important role. To date, a number of genes and pathways have been proposed to be associated with HTN, among which is Nitric Oxide pathway. NO levels can be regulated by reactive oxygen species (ROS), superoxide and post-transcriptional mechanisms, including sense-anti sense interactions. NOS3AS gene encodes an antisense RNA (sONE) which is complementary to NOS3 transcript in 662 nucleotides and may regulate NOS3 in a post-transcriptional manner. In this study, we sought to define the role of NOS3AS in the pathophysiology of essential HTN. A total of 131 cases with hypertension and 115 controls were enrolled in the study. Peripheral blood was drawn from all study participants after signing the informed consent form. Three variants (rs71539868, rs12666075 and rs7830) were investigated by Tetra-ARMS PCR method. The results were then statistically analyzed. We found statistically significant association between rs7830 TT genotype, rs12666075 GT and TT genotypes with susceptibility to HTN. We failed to observe association between rs71539868 and susceptibility to HTN. The present study showed a strong association between NOS3AS variants and susceptibility to hypertension in the population of Kermanshah province. Our results may shed more light on the mechanisms of disease development and may also help to better identify genetic predispositions and individuals at risk.

摘要

高血压(HTN)是一个全球性的健康挑战,增加了心血管疾病的风险。高血压的演变具有多因素的特点,遗传和环境因素都起着重要作用。迄今为止,已经提出了许多与 HTN 相关的基因和途径,其中包括一氧化氮途径。NO 水平可以通过活性氧(ROS)、超氧化物和转录后机制(包括反义-反义相互作用)进行调节。NOS3AS 基因编码一种反义 RNA(sONE),与 NOS3 转录物互补 662 个核苷酸,可能以转录后方式调节 NOS3。在这项研究中,我们试图确定 NOS3AS 在原发性高血压病理生理学中的作用。共纳入 131 例高血压患者和 115 例对照者。所有研究参与者在签署知情同意书后采集外周血。采用 Tetra-ARMS PCR 法检测 3 个变异体(rs71539868、rs12666075 和 rs7830)。然后对结果进行统计学分析。我们发现 rs7830 TT 基因型、rs12666075 GT 和 TT 基因型与高血压易感性之间存在统计学显著关联。我们没有观察到 rs71539868 与高血压易感性之间的关联。本研究显示 NOS3AS 变异与克尔曼沙阿省人群高血压易感性之间存在很强的关联。我们的研究结果可能为疾病发展的机制提供更多的线索,并有助于更好地识别遗传易感性和高危个体。

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本文引用的文献

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2
Identifying susceptibility genes for essential hypertension by transcriptome-wide association study.通过全转录组关联研究鉴定原发性高血压的易感基因。
Biochem Biophys Rep. 2022 Nov 21;32:101387. doi: 10.1016/j.bbrep.2022.101387. eCollection 2022 Dec.
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Alterations in endothelial nitric oxide synthase activity and their relevance to blood pressure.
内皮型一氧化氮合酶活性的改变及其与血压的相关性。
Biochem Pharmacol. 2022 Nov;205:115256. doi: 10.1016/j.bcp.2022.115256. Epub 2022 Sep 19.
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Global epidemiology, health burden and effective interventions for elevated blood pressure and hypertension.全球高血压流行病学、健康负担及有效干预措施
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Blood pressure and the new ACC/AHA hypertension guidelines.血压与新的 ACC/AHA 高血压指南。
Trends Cardiovasc Med. 2020 Apr;30(3):160-164. doi: 10.1016/j.tcm.2019.05.003. Epub 2019 May 15.
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Association of the gene polymorphisms with coronary artery disease susceptibility: A case-control study.基因多态性与冠状动脉疾病易感性的关联:一项病例对照研究。
J Cardiovasc Thorac Res. 2019;11(2):109-115. doi: 10.15171/jcvtr.2019.19. Epub 2019 Jun 25.
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Noncoding RNAs in Hypertension.高血压中的非编码RNA
Hypertension. 2019 Sep;74(3):477-492. doi: 10.1161/HYPERTENSIONAHA.119.13412. Epub 2019 Jul 29.
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