• 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

血清miR-132联合miR-223对脓毒症诱导的心肌病的诊断价值及意义

Diagnostic value and significance of serum miR-132 combined with miR-223 for sepsis-induced cardiomyopathy.

作者信息

Li Yanping, Lu Bin, Yu Muming, Zhai Jianhua, Yao Ying, Chai Yanfen

机构信息

Department of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.

出版信息

Exp Ther Med. 2021 Dec;22(6):1396. doi: 10.3892/etm.2021.10832. Epub 2021 Oct 1.

DOI:10.3892/etm.2021.10832
PMID:34650644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8506955/
Abstract

In previous studies, miR-132 and miR-223 were considered to be involved in cellular and pathological processes of diseases. However, the role of early diagnosis and prognosis evaluation in sepsis-induced cardiomyopathy (SIC) remains unknown. The present study aimed to explore the diagnostic value of combined detection of miR-132 and miR-223 for SIC and their correlation with creatine kinase-MB (CK-MB), cardiac troponin I (cTnI), tumor necrosis factor α (TNF-α), and interleukin-6 (IL)-6. SIC patients (n=80) admitted to Tianjin Medical University General Hospital were assigned to the research group (RG), while 60 healthy participants receiving physical examinations at the same period were assigned to the control group (CG). Serum expression profiles of miR-132 and miR-223 were detected by the RT-qPCR. CK-MB and cTnI were assessed using chemiluminescence assay, and TNF-α and IL-6 by enzyme-linked immunosorbent assay (ELISA). Serum miR-132 and miR-223 levels were significantly lower in the RG than in the CG (P<0.001). The sensitivity and specificity for the diagnosis of SIC were 82.50 and 71.67% for miR-132, 95.00 and 61.67% for miR-223, as well as 86.25 and 86.67% for miR-132 combined with miR-223. Serum miR-132 and miR-223 levels were significantly higher in the survivor group than in the deceased group (P<0.001). The sensitivity and specificity for the prognosis of SIC were 85.96 and 65.22% for miR-132 combined with miR-223. Serum miR-132 and miR-223 were negatively correlated with serum CK-MB, cTnI, TNF-α, and IL-6 (P<0.001). miR-132 combined with miR-223 can be used for early diagnosis and prognostic evaluation of SIC, and the two are correlated with CK-MB, cTnI, TNF-α, and IL-6.

摘要

在先前的研究中,miR - 132和miR - 223被认为参与了疾病的细胞和病理过程。然而,其在脓毒症诱导的心肌病(SIC)早期诊断和预后评估中的作用仍不清楚。本研究旨在探讨联合检测miR - 132和miR - 223对SIC的诊断价值及其与肌酸激酶同工酶(CK - MB)、心肌肌钙蛋白I(cTnI)、肿瘤坏死因子α(TNF - α)和白细胞介素 - 6(IL - 6)的相关性。将天津医科大学总医院收治的80例SIC患者纳入研究组(RG),同期60例接受体检的健康参与者纳入对照组(CG)。采用RT - qPCR检测血清中miR - 132和miR - 223的表达谱。采用化学发光法检测CK - MB和cTnI,采用酶联免疫吸附测定法(ELISA)检测TNF - α和IL - 6。研究组血清miR - 132和miR - 223水平显著低于对照组(P < 0.001)。miR - 132诊断SIC的灵敏度和特异度分别为82.50%和71.67%,miR - 223分别为95.00%和61.67%,miR - 132联合miR - 223分别为86.25%和86.67%。存活组血清miR - 132和miR - 223水平显著高于死亡组(P < 0.001)。miR - 132联合miR - 223对SIC预后评估的灵敏度和特异度分别为85.96%和65.22%。血清miR -

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/79d5c2edfb2a/etm-22-06-10832-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/7f43870c066c/etm-22-06-10832-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/df6017bcc6a0/etm-22-06-10832-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/4a778b39767a/etm-22-06-10832-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/79d5c2edfb2a/etm-22-06-10832-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/7f43870c066c/etm-22-06-10832-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/df6017bcc6a0/etm-22-06-10832-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/4a778b39767a/etm-22-06-10832-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/336b/8506955/79d5c2edfb2a/etm-22-06-10832-g03.jpg

相似文献

1
Diagnostic value and significance of serum miR-132 combined with miR-223 for sepsis-induced cardiomyopathy.血清miR-132联合miR-223对脓毒症诱导的心肌病的诊断价值及意义
Exp Ther Med. 2021 Dec;22(6):1396. doi: 10.3892/etm.2021.10832. Epub 2021 Oct 1.
2
[Value of combined detection of biomarkers in early diagnosis and prognosis of patients with septic myocardial injury].[生物标志物联合检测在脓毒症性心肌损伤患者早期诊断及预后评估中的价值]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2021 Apr;33(4):443-448. doi: 10.3760/cma.j.cn121430-20210128-00158.
3
MicroRNA-146a improves sepsis-induced cardiomyopathy by regulating the TLR-4/NF-κB signaling pathway.微小RNA-146a通过调节TLR-4/NF-κB信号通路改善脓毒症诱导的心肌病。
Exp Ther Med. 2019 Jul;18(1):779-785. doi: 10.3892/etm.2019.7657. Epub 2019 Jun 10.
4
Clinical value of microRNA-378a-3p in sepsis and its role in sepsis-induced inflammation and cardiac dysfunction.microRNA-378a-3p 在脓毒症中的临床价值及其在脓毒症诱导的炎症和心功能障碍中的作用。
Bioengineered. 2021 Dec;12(1):8496-8504. doi: 10.1080/21655979.2021.1985339.
5
[Experimental study of the effect of Shenmai injection on post-cardiac arrest syndrome in rabbit].[参麦注射液对兔心脏骤停后综合征影响的实验研究]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2013 Nov;25(11):664-8. doi: 10.3760/cma.j.issn.2095-4352.2013.11.007.
6
Diagnostic value of combined detection of IL-1β, IL-6, and TNF-α for sepsis-induced cardiomyopathy.白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α联合检测对脓毒症诱导的心肌病的诊断价值。
Med Clin (Barc). 2022 May 13;158(9):413-417. doi: 10.1016/j.medcli.2021.04.025. Epub 2021 Jun 17.
7
Low expression of microRNA-328 can predict sepsis and alleviate sepsis-induced cardiac dysfunction and inflammatory response.低表达的 microRNA-328 可以预测脓毒症,并减轻脓毒症引起的心脏功能障碍和炎症反应。
Braz J Med Biol Res. 2020 Jun 19;53(8):e9501. doi: 10.1590/1414-431X20209501. eCollection 2020.
8
Clinical significance of miR-492 in peripheral blood of acute myocardial infarction.miR-492 在急性心肌梗死患者外周血中的临床意义。
Eur Rev Med Pharmacol Sci. 2020 Sep;24(17):9041-9045. doi: 10.26355/eurrev_202009_22849.
9
Expression Levels of MicroRNA-146b and Anti-Cardiac Troponin I in Serum of Children with Viral Myocarditis and Their Clinical Significance.病毒性心肌炎患儿血清中MicroRNA-146b与抗心肌肌钙蛋白I的表达水平及其临床意义
Iran J Public Health. 2021 Mar;50(3):510-519. doi: 10.18502/ijph.v50i3.5592.
10
Clinical value and role of microRNA-29c-3p in sepsis-induced inflammation and cardiac dysfunction.miR-29c-3p 在脓毒症诱导的炎症和心功能障碍中的临床价值和作用。
Eur J Med Res. 2021 Aug 10;26(1):90. doi: 10.1186/s40001-021-00566-y.

引用本文的文献

1
MicroRNAs as regulators of cardiac dysfunction in sepsis: pathogenesis and diagnostic potential.微小RNA作为脓毒症心脏功能障碍的调节因子:发病机制及诊断潜力
Front Cardiovasc Med. 2025 Feb 18;12:1517323. doi: 10.3389/fcvm.2025.1517323. eCollection 2025.
2
The clinical effectiveness of sivelestat in treating sepsis patients with both acute respiratory distress syndrome and septic cardiomyopathy.西维来司他治疗急性呼吸窘迫综合征合并脓毒性心肌病脓毒症患者的临床疗效。
J Cardiothorac Surg. 2024 Jun 27;19(1):399. doi: 10.1186/s13019-024-02835-3.
3
Quercetin ameliorates ferroptosis of rat cardiomyocytes via activation of the SIRT1/p53/SLC7A11 signaling pathway to alleviate sepsis‑induced cardiomyopathy.

本文引用的文献

1
Circulatory miR-223-3p Discriminates Between Parkinson's and Alzheimer's Patients.循环 miR-223-3p 可区分帕金森病和阿尔茨海默病患者。
Sci Rep. 2019 Jun 28;9(1):9393. doi: 10.1038/s41598-019-45687-x.
2
HS attenuates sepsis-induced cardiac dysfunction via a PI3K/Akt-dependent mechanism.羟乙基淀粉通过PI3K/Akt依赖性机制减轻脓毒症诱导的心脏功能障碍。
Exp Ther Med. 2019 May;17(5):4064-4072. doi: 10.3892/etm.2019.7440. Epub 2019 Mar 26.
3
Levosimendan as a new force in the treatment of sepsis-induced cardiomyopathy: mechanism and clinical application.
槲皮素通过激活 SIRT1/p53/SLC7A11 信号通路改善大鼠心肌细胞铁死亡,从而减轻脓毒症诱导的心肌病。
Int J Mol Med. 2023 Dec;52(6). doi: 10.3892/ijmm.2023.5319. Epub 2023 Oct 20.
4
Modes of action and diagnostic value of miRNAs in sepsis.miRNAs 在脓毒症中的作用机制和诊断价值。
Front Immunol. 2022 Aug 5;13:951798. doi: 10.3389/fimmu.2022.951798. eCollection 2022.
左西孟旦作为治疗脓毒症诱导型心肌病的新力量:作用机制与临床应用
J Int Med Res. 2019 May;47(5):1817-1828. doi: 10.1177/0300060519837103. Epub 2019 Apr 8.
4
miR-146a Attenuates Sepsis-Induced Myocardial Dysfunction by Suppressing IRAK1 and TRAF6 via Targeting ErbB4 Expression.miR-146a 通过靶向 ErbB4 表达抑制 IRAK1 和 TRAF6 来减轻脓毒症诱导的心肌功能障碍。
Oxid Med Cell Longev. 2018 Aug 27;2018:7163057. doi: 10.1155/2018/7163057. eCollection 2018.
5
RETRACTED: LncRNA MALAT1 regulates sepsis-induced cardiac inflammation and dysfunction via interaction with miR-125b and p38 MAPK/NFκB.撤稿:长链非编码 RNA MALAT1 通过与 miR-125b 和 p38 MAPK/NFκB 的相互作用调节脓毒症引起的心脏炎症和功能障碍。
Int Immunopharmacol. 2018 Feb;55:69-76. doi: 10.1016/j.intimp.2017.11.038. Epub 2017 Dec 22.
6
Advances in Roles of miR-132 in the Nervous System.miR-132在神经系统中的作用研究进展
Front Pharmacol. 2017 Oct 25;8:770. doi: 10.3389/fphar.2017.00770. eCollection 2017.
7
IL-6 induced lncRNA MALAT1 enhances TNF-α expression in LPS-induced septic cardiomyocytes via activation of SAA3.白细胞介素-6诱导的长链非编码RNA MALAT1通过激活血清淀粉样蛋白A3增强脂多糖诱导的脓毒症心肌细胞中肿瘤坏死因子-α的表达。
Eur Rev Med Pharmacol Sci. 2017 Jan;21(2):302-309.
8
MicroRNA-135a is up-regulated and aggravates myocardial depression in sepsis via regulating p38 MAPK/NF-κB pathway.miRNA-135a 通过调控 p38MAPK/NF-κB 通路而上调,加重脓毒症心肌抑制。
Int Immunopharmacol. 2017 Apr;45:6-12. doi: 10.1016/j.intimp.2017.01.029. Epub 2017 Jan 29.
9
MicroRNA-132 attenuates neurobehavioral and neuropathological changes associated with intracerebral hemorrhage in mice.微小RNA-132减轻小鼠脑出血相关的神经行为和神经病理变化。
Neurochem Int. 2017 Jul;107:182-190. doi: 10.1016/j.neuint.2016.11.011. Epub 2016 Dec 9.
10
Inhibition of miR-155 Protects Against LPS-induced Cardiac Dysfunction and Apoptosis in Mice.抑制miR-155可预防小鼠内毒素诱导的心脏功能障碍和细胞凋亡。
Mol Ther Nucleic Acids. 2016 Oct 11;5(10):e374. doi: 10.1038/mtna.2016.80.