• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血浆 miR-195-5p 可预测住院新冠患者的严重程度。

Plasma miR-195-5p predicts the severity of Covid-19 in hospitalized patients.

机构信息

Department of Biochemistry and Pharmacology, Discipline of Biochemistry, University of Medicine and Pharmacy "Victor Babes", E Murgu Square no.2, 300041, Timisoara, Romania.

Doctoral School, University of Medicine and Pharmacy "Victor Babes", E Murgu Square no.2, 300041, Timisoara, Romania.

出版信息

Sci Rep. 2023 Aug 23;13(1):13806. doi: 10.1038/s41598-023-40754-w.

DOI:10.1038/s41598-023-40754-w
PMID:37612439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10447562/
Abstract

Predicting the clinical course of Covid-19 is a challenging task, given the multi-systemic character of the disease and the paucity of minimally invasive biomarkers of disease severity. Here, we evaluated the early (first two days post-admission) level of circulating hsa-miR-195-5p (miR-195, a known responder to viral infections and SARS-CoV-2 interactor) in Covid-19 patients and assessed its potential as a biomarker of disease severity. We show that plasma miR-195 correlates with several clinical and paraclinical parameters, and is an excellent discriminator between the severe and mild forms of the disease. Our Gene Ontology analysis of miR-195 targets differentially expressed in Covid-19 indicates a strong impact on cardiac mitochondria homeostasis, suggesting a possible role in long Covid and chronic fatigue syndrome (CFS) syndromes.

摘要

预测新冠病毒(Covid-19)的临床病程是一项极具挑战性的任务,因为该疾病具有多系统特征,且缺乏疾病严重程度的微创生物标志物。在此,我们评估了新冠病毒患者入院后最初两天(即早期)的循环 hsa-miR-195-5p(miR-195,一种已知的病毒感染应答物和 SARS-CoV-2 相互作用物)水平,并评估了其作为疾病严重程度生物标志物的潜力。我们发现,血浆 miR-195 与多项临床和临床前参数相关,且是区分疾病严重程度和轻度程度的优秀判别物。我们对新冠病毒患者中差异表达的 miR-195 靶基因的基因本体分析表明,其对心脏线粒体动态平衡具有强烈影响,这表明其可能与长新冠和慢性疲劳综合征(CFS)综合征有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b02/10447562/6ec575165eef/41598_2023_40754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b02/10447562/9915757829a6/41598_2023_40754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b02/10447562/6ec575165eef/41598_2023_40754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b02/10447562/9915757829a6/41598_2023_40754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b02/10447562/6ec575165eef/41598_2023_40754_Fig2_HTML.jpg

相似文献

1
Plasma miR-195-5p predicts the severity of Covid-19 in hospitalized patients.血浆 miR-195-5p 可预测住院新冠患者的严重程度。
Sci Rep. 2023 Aug 23;13(1):13806. doi: 10.1038/s41598-023-40754-w.
2
Saliva antibody-fingerprint of reactivated latent viruses after mild/asymptomatic COVID-19 is unique in patients with myalgic-encephalomyelitis/chronic fatigue syndrome.轻度/无症状 COVID-19 后潜伏病毒再激活的唾液抗体指纹在肌痛性脑脊髓炎/慢性疲劳综合征患者中是独特的。
Front Immunol. 2022 Oct 20;13:949787. doi: 10.3389/fimmu.2022.949787. eCollection 2022.
3
Cellular miR-150-5p may have a crucial role to play in the biology of SARS-CoV-2 infection by regulating gene.细胞 miR-150-5p 通过调控基因,可能在 SARS-CoV-2 感染的生物学中发挥关键作用。
RNA Biol. 2022;19(1):1-11. doi: 10.1080/15476286.2021.2010959. Epub 2021 Dec 31.
4
Differentially expressed plasmatic microRNAs in Brazilian patients with Coronavirus disease 2019 (COVID-19): preliminary results.巴西 2019 冠状病毒病(COVID-19)患者血浆差异表达的 microRNAs:初步结果。
Mol Biol Rep. 2022 Jul;49(7):6931-6943. doi: 10.1007/s11033-022-07338-9. Epub 2022 Mar 17.
5
Differential microRNA expression in the peripheral blood from human patients with COVID-19.COVID-19 患者外周血中的差异 microRNA 表达。
J Clin Lab Anal. 2020 Oct;34(10):e23590. doi: 10.1002/jcla.23590. Epub 2020 Sep 22.
6
Genetic risk factors for severe and fatigue dominant long COVID and commonalities with ME/CFS identified by combinatorial analysis.通过组合分析确定的严重和疲劳主导的长新冠的遗传风险因素,以及与 ME/CFS 的共同特征。
J Transl Med. 2023 Nov 1;21(1):775. doi: 10.1186/s12967-023-04588-4.
7
IFI44 is an immune evasion biomarker for SARS-CoV-2 and infection in patients with RA.IFI44 是 SARS-CoV-2 的免疫逃逸生物标志物,与 RA 患者的感染相关。
Front Immunol. 2022 Sep 15;13:1013322. doi: 10.3389/fimmu.2022.1013322. eCollection 2022.
8
The expression patterns of MALAT-1, NEAT-1, THRIL, and miR-155-5p in the acute to the post-acute phase of COVID-19 disease.MALAT-1、NEAT-1、THRIL 和 miR-155-5p 在 COVID-19 疾病的急性期到亚急性期的表达模式。
Braz J Infect Dis. 2022 May-Jun;26(3):102354. doi: 10.1016/j.bjid.2022.102354. Epub 2022 Apr 25.
9
Upregulation of hsa_circ_0004812 promotes COVID-19 cytokine storm via hsa-miR-1287-5p/IL6R, RIG-I axis.环状 RNA hsa_circ_0004812 通过 hsa-miR-1287-5p/IL6R、RIG-I 轴上调促进 COVID-19 细胞因子风暴。
J Clin Lab Anal. 2022 Oct;36(10):e24666. doi: 10.1002/jcla.24666. Epub 2022 Aug 21.
10
Differential gene expression profiling reveals potential biomarkers and pharmacological compounds against SARS-CoV-2: Insights from machine learning and bioinformatics approaches.差异基因表达谱分析揭示了针对 SARS-CoV-2 的潜在生物标志物和药物化合物:机器学习和生物信息学方法的见解。
Front Immunol. 2022 Aug 17;13:918692. doi: 10.3389/fimmu.2022.918692. eCollection 2022.

引用本文的文献

1
MicroRNAs in long COVID: roles, diagnostic biomarker potential and detection.长新冠中的微小RNA:作用、诊断生物标志物潜力及检测
Hum Genomics. 2025 Aug 13;19(1):90. doi: 10.1186/s40246-025-00810-0.
2
A Nomogram for Predicting Survival in Patients with SARS-CoV-2 Omicron Variant Pneumonia Based on Admission Data.基于入院数据预测新冠病毒奥密克戎变异株肺炎患者生存情况的列线图
Infect Drug Resist. 2025 Apr 25;18:2093-2104. doi: 10.2147/IDR.S509178. eCollection 2025.
3
Cytosolic nucleic acid sensing as driver of critical illness: mechanisms and advances in therapy.

本文引用的文献

1
The SARS-CoV-2 protein NSP2 impairs the silencing capacity of the human 4EHP-GIGYF2 complex.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)蛋白NSP2会损害人类4EHP-GIGYF2复合物的沉默能力。
iScience. 2022 Jul 15;25(7):104646. doi: 10.1016/j.isci.2022.104646. Epub 2022 Jun 20.
2
Altered microRNA expression in severe COVID-19: Potential prognostic and pathophysiological role.重症新型冠状病毒肺炎中微小RNA表达的改变:潜在的预后及病理生理作用
Clin Transl Med. 2022 Jun;12(6):e899. doi: 10.1002/ctm2.899.
3
Combined kinetic analysis of SARS-CoV-2 RNAemia, N-antigenemia and virus-specific antibodies in critically ill adult COVID-19 patients.
胞质核酸感应作为危重症的驱动因素:机制与治疗进展
Signal Transduct Target Ther. 2025 Mar 19;10(1):90. doi: 10.1038/s41392-025-02174-2.
4
Changes in miRNA Pattern Expression Associated With COVID-19 Severity.与新冠病毒疾病严重程度相关的微小RNA模式表达变化
In Vivo. 2025 Jan-Feb;39(1):482-490. doi: 10.21873/invivo.13852.
5
SARS-CoV-2 Vaccine Improved Hemostasis of a Patient with Protein S Deficiency: A Case Report.SARS-CoV-2 疫苗改善了蛋白 S 缺乏症患者的止血功能:一例报告。
Int J Mol Sci. 2024 Oct 5;25(19):10717. doi: 10.3390/ijms251910717.
6
The potential of circulating microRNAs as novel diagnostic biomarkers of COVID-19: a systematic review and meta-analysis.循环 microRNAs 作为 COVID-19 新型诊断生物标志物的潜力:系统评价和荟萃分析。
BMC Infect Dis. 2024 Sep 19;24(1):1011. doi: 10.1186/s12879-024-09915-8.
7
The relationship between microRNAs and COVID-19 complications.微小RNA与新型冠状病毒肺炎并发症之间的关系。
Noncoding RNA Res. 2024 Aug 22;10:16-24. doi: 10.1016/j.ncrna.2024.08.007. eCollection 2025 Feb.
8
Identifying microRNAs Possibly Implicated in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Fibromyalgia: A Review.鉴定可能与肌痛性脑脊髓炎/慢性疲劳综合征和纤维肌痛有关的 microRNAs:综述。
Int J Mol Sci. 2024 Sep 3;25(17):9551. doi: 10.3390/ijms25179551.
9
Mitochondria in COVID-19: from cellular and molecular perspective.新型冠状病毒肺炎中的线粒体:从细胞和分子角度看
Front Physiol. 2024 Jun 21;15:1406635. doi: 10.3389/fphys.2024.1406635. eCollection 2024.
10
Alteration of circulating ACE2-network related microRNAs in patients with COVID-19.新型冠状病毒肺炎患者循环 ACE2 网络相关 microRNAs 的变化。
Sci Rep. 2024 Jun 12;14(1):13573. doi: 10.1038/s41598-024-58037-3.
严重成人 COVID-19 患者中 SARS-CoV-2 RNA 血症、N 抗原血症和病毒特异性抗体的联合动力学分析。
Sci Rep. 2022 May 18;12(1):8273. doi: 10.1038/s41598-022-12461-5.
4
SARS-COV-2 as potential microRNA sponge in COVID-19 patients.SARS-CoV-2 作为 COVID-19 患者中的潜在 miRNA 海绵。
BMC Med Genomics. 2022 Apr 23;15(Suppl 2):94. doi: 10.1186/s12920-022-01243-7.
5
Cardiovascular signatures of COVID-19 predict mortality and identify barrier stabilizing therapies.新冠病毒病的心血管特征可预测死亡率并确定稳定屏障的治疗方法。
EBioMedicine. 2022 Apr;78:103982. doi: 10.1016/j.ebiom.2022.103982. Epub 2022 Apr 8.
6
System-wide transcriptome damage and tissue identity loss in COVID-19 patients.新冠肺炎患者的全系统转录组损伤和组织特征丧失。
Cell Rep Med. 2022 Jan 24;3(2):100522. doi: 10.1016/j.xcrm.2022.100522. eCollection 2022 Feb 15.
7
Multiple early factors anticipate post-acute COVID-19 sequelae.多种早期因素预示着急性新冠病毒感染后会出现长期新冠症状。
Cell. 2022 Mar 3;185(5):881-895.e20. doi: 10.1016/j.cell.2022.01.014. Epub 2022 Jan 25.
8
miR-155: A Potential Biomarker for Predicting Mortality in COVID-19 Patients.微小RNA-155:一种预测COVID-19患者死亡率的潜在生物标志物。
J Pers Med. 2022 Feb 21;12(2):324. doi: 10.3390/jpm12020324.
9
Plasma miRNA profile at COVID-19 onset predicts severity status and mortality.新冠肺炎发病时的血浆 miRNA 谱可预测严重程度和死亡率。
Emerg Microbes Infect. 2022 Dec;11(1):676-688. doi: 10.1080/22221751.2022.2038021.
10
Circulating miR-320b and miR-483-5p levels are associated with COVID-19 in-hospital mortality.循环 miR-320b 和 miR-483-5p 水平与 COVID-19 院内死亡率相关。
Mech Ageing Dev. 2022 Mar;202:111636. doi: 10.1016/j.mad.2022.111636. Epub 2022 Feb 2.