• 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

miR-210、miR-494 和 miR-205 在中老年脓毒症相关性急性肾损伤患者中的表达模式及预后价值。

Expression patterns and prognostic value of miR-210, miR-494, and miR-205 in middle-aged and old patients with sepsis-induced acute kidney injury.

机构信息

Department of Intensive Care Unit, Sir Run Run Shaw Hospital, Medicine School of Zhejiang University, Hangzhou, China.

出版信息

Bosn J Basic Med Sci. 2019 Aug 20;19(3):249-256. doi: 10.17305/bjbms.2019.4131.

DOI:10.17305/bjbms.2019.4131
PMID:30997877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6716103/
Abstract

Septic patients suffer a 'cytokine storm' from proinflammatory cytokines, chemokines and other inflammatory mediators, resulting in acute kidney injury (AKI) and death. The purpose of the present study was to determine the expression patterns of microRNA-210 (miR-210), miR-494, and miR-205 in middle-aged and old patients with sepsis-induced AKI and to evaluate their association with patient prognosis. Serum blood urea nitrogen (BUN), creatinine (Cr) and cystatin C levels were determined in peripheral venous blood collected from 110 patients with sepsis-induced AKI and 110 healthy controls. The expression profile of 30 miRNAs was analyzed by TaqMan low-density array (TLDA) in plasma samples from patients and controls. Association of miRNAs with prognosis and survival of patients was analyzed by Spearman's rank correlation coefficient, Cox multivariate analysis, and ROC curve analysis. TILDA analysis showed 11 upregulated and 11 downregulated miRNAs in patients with sepsis-induced AKI. MiR-210 and miR-494 were the most upregulated and miR-205 was the most downregulated miRNA. High expression of miR-210 and miR-494 was positively correlated with BUN, Cr and cystatin C levels of patients, while low expression of miR-205 was negatively correlated. MiR-210 and miR-494 expression was significantly decreased and miR-205 expression was increased in survivors with sepsis-induced AKI (28-day survival, n = 68) vs. non-survivors (n = 42). BUN, Cr, and miR-205 were independent risk factors for prognosis in sepsis-induced AKI. Our study showed the predictive value of miR-210, miR-494, and miR-205 in prognosis and survival of patients with sepsis-induced AKI. MiR-205 is an independent risk factor for sepsis-induced AKI and its decreased expression is associated with shorter patient survival.

摘要

脓毒症患者会遭受促炎细胞因子、趋化因子和其他炎症介质引起的“细胞因子风暴”,导致急性肾损伤(AKI)和死亡。本研究旨在确定中老年人脓毒症诱导的 AKI 患者中 microRNA-210 (miR-210)、miR-494 和 miR-205 的表达模式,并评估它们与患者预后的关系。采集 110 例脓毒症诱导 AKI 患者和 110 例健康对照者外周静脉血,检测血清血尿素氮(BUN)、肌酐(Cr)和胱抑素 C 水平。采用 TaqMan 低密度阵列(TLDA)分析患者和对照者血浆样本中的 30 种 miRNA 的表达谱。采用 Spearman 秩相关系数、Cox 多因素分析和 ROC 曲线分析 miRNA 与患者预后和生存的关系。TILDA 分析显示,脓毒症诱导 AKI 患者有 11 种上调和 11 种下调 miRNA。miR-210 和 miR-494 表达上调最显著,miR-205 表达下调最显著。miR-210 和 miR-494 的高表达与患者 BUN、Cr 和胱抑素 C 水平呈正相关,而 miR-205 的低表达与 BUN、Cr 和胱抑素 C 水平呈负相关。脓毒症诱导 AKI 存活者(28 天存活,n = 68)与非存活者(n = 42)相比,miR-210 和 miR-494 表达明显降低,miR-205 表达升高。BUN、Cr 和 miR-205 是脓毒症诱导 AKI 预后的独立危险因素。本研究表明,miR-210、miR-494 和 miR-205 对脓毒症诱导 AKI 患者的预后和生存具有预测价值。miR-205 是脓毒症诱导 AKI 的独立危险因素,其表达降低与患者生存时间缩短有关。

相似文献

1
Expression patterns and prognostic value of miR-210, miR-494, and miR-205 in middle-aged and old patients with sepsis-induced acute kidney injury.miR-210、miR-494 和 miR-205 在中老年脓毒症相关性急性肾损伤患者中的表达模式及预后价值。
Bosn J Basic Med Sci. 2019 Aug 20;19(3):249-256. doi: 10.17305/bjbms.2019.4131.
2
Deregulated microRNA-22-3p in patients with sepsis-induced acute kidney injury serves as a new biomarker to predict disease occurrence and 28-day survival outcomes.在脓毒症诱导的急性肾损伤患者中,失调的 microRNA-22-3p 可作为一种新的生物标志物,用于预测疾病发生和 28 天的生存结局。
Int Urol Nephrol. 2021 Oct;53(10):2107-2116. doi: 10.1007/s11255-021-02784-z. Epub 2021 Jan 28.
3
Differentially expressed miRNAs in sepsis-induced acute kidney injury target oxidative stress and mitochondrial dysfunction pathways.脓毒症诱导的急性肾损伤中差异表达的微小RNA靶向氧化应激和线粒体功能障碍通路。
PLoS One. 2017 Mar 15;12(3):e0173292. doi: 10.1371/journal.pone.0173292. eCollection 2017.
4
[Predictive value of miRNA-29a and miRNA-10a-5p for 28-day mortality in patients with sepsis-induced acute kidney injury].[miRNA-29a和miRNA-10a-5p对脓毒症诱导的急性肾损伤患者28天死亡率的预测价值]
Nan Fang Yi Ke Da Xue Xue Bao. 2017 May 20;37(5):646-651. doi: 10.3969/j.issn.1673-4254.2017.05.13.
5
Comparison of Neutrophil Gelatinase-Associated Lipocalin Versus B-Type Natriuretic Peptide and Cystatin C to Predict Early Acute Kidney Injury and Outcome in Patients With Acute Heart Failure.中性粒细胞明胶酶相关脂质运载蛋白与B型利钠肽及胱抑素C在预测急性心力衰竭患者早期急性肾损伤及预后中的比较
Am J Cardiol. 2015 Jul 1;116(1):104-11. doi: 10.1016/j.amjcard.2015.03.043. Epub 2015 Apr 8.
6
Predictive ability of circulating osteoprotegerin as a novel biomarker for early detection of acute kidney injury induced by sepsis.循环骨保护素作为早期检测脓毒症诱导的急性肾损伤新生物标志物的预测能力
Eur Cytokine Netw. 2017 Jun 1;28(2):52-62. doi: 10.1684/ecn.2017.0393.
7
Impact of sepsis on levels of plasma cystatin C in AKI and non-AKI patients.脓毒症对 AKI 及非 AKI 患者血浆胱抑素 C 水平的影响。
Nephrol Dial Transplant. 2012 Feb;27(2):576-81. doi: 10.1093/ndt/gfr358. Epub 2011 Sep 12.
8
Correlation Between Single Nucleotide Polymorphisms at the 3'-UTR of the Gene and Acute Kidney Injury in Sepsis.基因 3'-UTR 单核苷酸多态性与脓毒症急性肾损伤的相关性。
Genet Test Mol Biomarkers. 2020 May;24(5):274-284. doi: 10.1089/gtmb.2019.0222. Epub 2020 Apr 21.
9
Downregulation of miR-574-5p inhibits HK-2 cell viability and predicts the onset of acute kidney injury in sepsis patients.下调 miR-574-5p 抑制 HK-2 细胞活力,并预测脓毒症患者急性肾损伤的发生。
Ren Fail. 2021 Dec;43(1):942-948. doi: 10.1080/0886022X.2021.1939051.
10
Clinical value of serum miR-320-3p expression in predicting the prognosis of sepsis-induced acute kidney injury.血清 miR-320-3p 表达在预测脓毒症相关性急性肾损伤预后中的临床价值。
J Clin Lab Anal. 2022 May;36(5):e24358. doi: 10.1002/jcla.24358. Epub 2022 Mar 25.

引用本文的文献

1
The potential role of non-coding RNAs in acute kidney injury: a focus on natural medicine treatment.非编码RNA在急性肾损伤中的潜在作用:聚焦于天然药物治疗
Front Mol Biosci. 2025 Aug 7;12:1648526. doi: 10.3389/fmolb.2025.1648526. eCollection 2025.
2
Predictive value of combined detection of blood Urea nitrogen and Neutrophil-to-lymphocyte ratio for identifying severe pneumonia complicated with sepsis in neonates.血尿素氮与中性粒细胞与淋巴细胞比值联合检测对新生儿重症肺炎合并脓毒症的预测价值
BMC Infect Dis. 2025 Aug 19;25(1):1045. doi: 10.1186/s12879-025-11471-8.
3
Significances of miRNAs for predicting sepsis mortality: a meta-analysis.微小RNA用于预测脓毒症死亡率的意义:一项荟萃分析
Front Microbiol. 2025 Mar 11;16:1472124. doi: 10.3389/fmicb.2025.1472124. eCollection 2025.
4
Albumin corrected anion gap and clinical outcomes in elderly patients with acute kidney injury caused or accompanied by sepsis: a MIMIC-IV retrospective study.白蛋白校正阴离子间隙与脓毒症所致或伴发急性肾损伤老年患者的临床结局:一项MIMIC-IV回顾性研究
Eur J Med Res. 2025 Jan 7;30(1):11. doi: 10.1186/s40001-024-02238-z.
5
Evaluation of microRNA-10a and microRNA-210 as Biomarkers in Sepsis Patients With Acute Kidney Injury.评估微小RNA-10a和微小RNA-210作为急性肾损伤脓毒症患者生物标志物的作用
Int J Nephrol. 2024 Dec 12;2024:1555811. doi: 10.1155/ijne/1555811. eCollection 2024.
6
Systematic review of microRNAs in human acute kidney injury.系统评价人类急性肾损伤中的 microRNAs。
Ren Fail. 2024 Dec;46(2):2419960. doi: 10.1080/0886022X.2024.2419960. Epub 2024 Oct 30.
7
A Systematic Review and Meta-Analysis of MicroRNA as Predictive Biomarkers of Acute Kidney Injury.微小RNA作为急性肾损伤预测生物标志物的系统评价与Meta分析
Biomedicines. 2024 Jul 30;12(8):1695. doi: 10.3390/biomedicines12081695.
8
Exosomes derived from endothelial progenitor cells ameliorate LPS-induced brain microvascular endothelial cells injury by delivering miR-126a-5p.内皮祖细胞来源的外泌体通过递送 miR-126a-5p 减轻 LPS 诱导的脑微血管内皮细胞损伤。
Sci Rep. 2024 Aug 9;14(1):18469. doi: 10.1038/s41598-024-69163-3.
9
Comprehensive analysis of ceRNA network composed of circRNA, miRNA, and mRNA in septic acute kidney injury patients based on RNA-seq.基于RNA测序对脓毒症急性肾损伤患者中由环状RNA、微小RNA和信使RNA组成的竞争性内源RNA网络进行综合分析。
Front Genet. 2023 Sep 14;14:1209042. doi: 10.3389/fgene.2023.1209042. eCollection 2023.
10
MicroRNAs as Biomarkers and Therapeutic Targets for Acute Kidney Injury.微小RNA作为急性肾损伤的生物标志物和治疗靶点
Diagnostics (Basel). 2023 Sep 9;13(18):2893. doi: 10.3390/diagnostics13182893.

本文引用的文献

1
The meaning of the blood urea nitrogen/creatinine ratio in acute kidney injury.急性肾损伤中血尿素氮/肌酐比值的意义。
Clin Kidney J. 2012 Apr;5(2):187-191. doi: 10.1093/ckj/sfs013.
2
up-regulates the PI3K/Akt pathway via targetting PTEN and attenuates hepatic ischemia/reperfusion injury in a rat model.通过靶向 PTEN 上调 PI3K/Akt 通路,减轻大鼠肝缺血/再灌注损伤。
Biosci Rep. 2017 Sep 19;37(5). doi: 10.1042/BSR20170798. Print 2017 Oct 31.
3
[Predictive value of miRNA-29a and miRNA-10a-5p for 28-day mortality in patients with sepsis-induced acute kidney injury].[miRNA-29a和miRNA-10a-5p对脓毒症诱导的急性肾损伤患者28天死亡率的预测价值]
Nan Fang Yi Ke Da Xue Xue Bao. 2017 May 20;37(5):646-651. doi: 10.3969/j.issn.1673-4254.2017.05.13.
4
Differentially expressed miRNAs in sepsis-induced acute kidney injury target oxidative stress and mitochondrial dysfunction pathways.脓毒症诱导的急性肾损伤中差异表达的微小RNA靶向氧化应激和线粒体功能障碍通路。
PLoS One. 2017 Mar 15;12(3):e0173292. doi: 10.1371/journal.pone.0173292. eCollection 2017.
5
MicroRNA-205‑5b inhibits HMGB1 expression in LPS-induced sepsis.微小RNA-205-5b抑制脂多糖诱导的脓毒症中高迁移率族蛋白B1的表达。
Int J Mol Med. 2016 Jul;38(1):312-8. doi: 10.3892/ijmm.2016.2613. Epub 2016 May 27.
6
Diagnostic value of elevated serum miRNA-143 levels in sepsis.血清miRNA-143水平升高在脓毒症中的诊断价值
J Int Med Res. 2016 Aug;44(4):875-81. doi: 10.1177/0300060516645003. Epub 2016 May 25.
7
Identification of urinary microRNA biomarkers for detection of gentamicin-induced acute kidney injury in rats.用于检测庆大霉素诱导的大鼠急性肾损伤的尿液微小RNA生物标志物的鉴定
Regul Toxicol Pharmacol. 2016 Jul;78:78-84. doi: 10.1016/j.yrtph.2016.04.001. Epub 2016 Apr 10.
8
The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).《脓毒症及脓毒性休克第三次国际共识定义(脓毒症-3)》
JAMA. 2016 Feb 23;315(8):801-10. doi: 10.1001/jama.2016.0287.
9
Splenic RNA and MicroRNA Mimics Promote Complement Factor B Production and Alternative Pathway Activation via Innate Immune Signaling.脾脏RNA和微小RNA模拟物通过天然免疫信号促进补体因子B的产生和替代途径激活。
J Immunol. 2016 Mar 15;196(6):2788-98. doi: 10.4049/jimmunol.1502106. Epub 2016 Feb 17.
10
Circulating MicroRNAs as Biomarkers for Sepsis.循环微小RNA作为脓毒症的生物标志物
Int J Mol Sci. 2016 Jan 9;17(1):78. doi: 10.3390/ijms17010078.