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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.

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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