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SERBP1(Hero45)是与缺血性心脏病风险相关的新联系:与冠状动脉阻塞、血液凝固和血脂谱的关联

"SERBP1 (Hero45) is a Novel Link with Ischemic Heart Disease Risk: Associations with Coronary Arteries Occlusion, Blood Coagulation and Lipid Profile".

作者信息

Shilenok Vladislav, Kobzeva Ksenia, Bushueva Olga

机构信息

Laboratory of Genomic Research, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, Kursk, Russia.

Cardiology Department with the intensive care unit, Kursk Emergency Hospital, Kursk, Russia.

出版信息

Cell Biochem Biophys. 2025 Apr 3. doi: 10.1007/s12013-025-01736-z.

DOI:10.1007/s12013-025-01736-z
PMID:40175693
Abstract

Ischemic heart disease (IHD), stemming from coronary atherosclerosis, involves pathological processes in which chaperone proteins play an essential role. SERBP1 (Hero45), an RNA-binding protein, has recently been ascribed to the newly discovered class of Hero proteins with chaperone-like activity, making it particularly relevant in atherosclerosis-related diseases. In this study, 2164 subjects (836 IHD patients and 1328 controls) were genotyped for five common single nucleotide polymorphisms (SNPs) of SERBP1 using probe-based PCR. Here, we report that SNPs of SERBP1 are associated with reduced risk of left coronary artery atherosclerosis: rs4655707 (effect allele [EA] T, OR = 0.63, 95% CI 0.43-0.93, p = 0.02), (EA C, OR = 0.63, 95% CI 0.42-0.95, p = 0.02), rs12561767 (EA G, OR = 0.65, 95% CI 0.45-0.96, p = 0.03), rs6702742 (EA A, OR = 0.63, 95% CI 0.43-0.94, p = 0.02). Additionally, SERBP1 loci are linked to lower coronary artery stenosis (rs1058074), improved blood lipid profiles (rs1058074), and favorable blood coagulation parameters (rs4655707, rs6702742, rs1058074, rs12561767). Together, our study is the first to provide evidence that SERBP1 is involved in lipid metabolism and coagulation regulation, modulating IHD risk.

摘要

缺血性心脏病(IHD)源于冠状动脉粥样硬化,涉及伴侣蛋白发挥重要作用的病理过程。SERBP1(Hero45)是一种RNA结合蛋白,最近被归入新发现的具有伴侣样活性的Hero蛋白类别,这使其在动脉粥样硬化相关疾病中具有特别重要的意义。在本研究中,使用基于探针的PCR对2164名受试者(836名IHD患者和1328名对照)的SERBP1的五个常见单核苷酸多态性(SNP)进行基因分型。在此,我们报告SERBP1的SNP与左冠状动脉粥样硬化风险降低相关:rs4655707(效应等位基因[EA]T,OR = 0.63,95%CI 0.43 - 0.93,p = 0.02),(EA C,OR = 0.63,95%CI 0.42 - 0.95,p = 0.02),rs12561767(EA G,OR = 0.65,95%CI 0.45 - 0.96,p = 0.03),rs6702742(EA A,OR = 0.63,95%CI 0.43 - 0.94,p = 0.02)。此外,SERBP1基因座与较低的冠状动脉狭窄(rs1058074)、改善的血脂谱(rs1058074)和良好的凝血参数(rs4655707、rs6702742、rs1058074、rs12561767)相关。总之,我们的研究首次提供证据表明SERBP1参与脂质代谢和凝血调节,调节IHD风险。

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本文引用的文献

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Front Biosci (Schol Ed). 2024 Dec 11;16(4):19. doi: 10.31083/j.fbs1604019.
2
Polymorphism in Genes Encoding HSP40 Family Proteins is Associated with Ischemic Stroke Risk and Brain Infarct Size: A Pilot Study.编码HSP40家族蛋白的基因多态性与缺血性中风风险及脑梗死大小相关:一项初步研究。
J Integr Neurosci. 2024 Dec 4;23(12):211. doi: 10.31083/j.jin2312211.
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Chaperones vs. oxidative stress in the pathobiology of ischemic stroke.
伴侣蛋白与氧化应激在缺血性脑卒中病理生物学中的作用
Front Mol Neurosci. 2024 Dec 11;17:1513084. doi: 10.3389/fnmol.2024.1513084. eCollection 2024.
4
Adipsin improves diabetic hindlimb ischemia through SERPINE1 dependent angiogenesis.脂联素通过依赖于丝氨酸蛋白酶抑制剂E1的血管生成改善糖尿病后肢缺血。
Cardiovasc Diabetol. 2024 Dec 2;23(1):429. doi: 10.1186/s12933-024-02526-2.
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(Hero20) Gene Polymorphism: Contribution to Ischemic Stroke Risk and Interactions with Other Heat-Resistant Obscure Chaperones.(Hero20)基因多态性:对缺血性中风风险的贡献以及与其他耐热性不明伴侣蛋白的相互作用
Biomedicines. 2024 Nov 14;12(11):2603. doi: 10.3390/biomedicines12112603.
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Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease.与冠状动脉疾病相比,主动脉瓣狭窄的独特遗传风险特征。
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Life (Basel). 2024 Sep 12;14(9):1158. doi: 10.3390/life14091158.
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RNA. 2024 Oct 16;30(11):1422-1436. doi: 10.1261/rna.080165.124.
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