• 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-370-3p 和 miR-495-3p 作为脓毒症相关性急性肾损伤生物标志物的潜力。

The Potential of miR-370-3p and miR-495-3p Serving as Biomarkers for Sepsis-Associated Acute Kidney Injury.

机构信息

Department of Nephrology, SINOPHARM North Hospital, Baotou, 014030 Inner Mongolia, China.

出版信息

Comput Math Methods Med. 2022 Jul 11;2022:2439509. doi: 10.1155/2022/2439509. eCollection 2022.

DOI:10.1155/2022/2439509
PMID:35860182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9293507/
Abstract

OBJECTIVE

This study is aimed at evaluating the miR-370-3p and miR-495-3p expression in the urine of patients with sepsis-associated acute kidney injury (SA-AKI) and exploring its diagnosis value in for SA-AKI.

METHODS

184 sepsis invalids were collected and divided two groups (non-AKI group or AKI group) according to whether they had acute kidney injury. RT-qPCR was utilized to measure miR-370-3p and miR-495-3p expressions. ROC curve was performed to evaluate the diagnostic value of miR-370-3p and miR-495-3p for SA-AKI. Patients diagnosed with SA-AKI were followed up for 28 days to record survival time. The prognostic performance of miR-370-3p and miR-495-3p for SA-AKI was evaluated by survival curves.

RESULTS

Compared with non-AKI invalids, miR-370-3p and miR-495-3p expressions were obviously lower in the urine of AKI invalids. miR-370-3p and miR-495-3p expressions were markedly negatively correlated with biomarkers of renal injury. Furthermore, the area under the curve (AUC) of miR-370-3p and miR-495-3p for diagnosing sepsis SA-AKI was 0.896 and 0.814, respectively. The higher 28 days-survival rate was observed in patients with high miR-370-3p and miR-495-3p expressions.

CONCLUSIONS

A novel biomarker for the early diagnosis of SA-AKI may be miR-370-3p and miR-495-3p, which was clearly reduced in the urine of SA-AKI patients.

摘要

目的

本研究旨在评估脓毒症相关性急性肾损伤(SA-AKI)患者尿液中 miR-370-3p 和 miR-495-3p 的表达情况,并探讨其在 SA-AKI 诊断中的价值。

方法

收集 184 例脓毒症患者,根据是否发生急性肾损伤分为非 AKI 组或 AKI 组。利用 RT-qPCR 测量 miR-370-3p 和 miR-495-3p 的表达。绘制 ROC 曲线评估 miR-370-3p 和 miR-495-3p 对 SA-AKI 的诊断价值。对诊断为 SA-AKI 的患者进行 28 天随访,记录生存时间。通过生存曲线评估 miR-370-3p 和 miR-495-3p 对 SA-AKI 的预后性能。

结果

与非 AKI 患者相比,AKI 患者尿液中 miR-370-3p 和 miR-495-3p 的表达明显降低。miR-370-3p 和 miR-495-3p 的表达与肾损伤标志物呈明显负相关。此外,miR-370-3p 和 miR-495-3p 诊断脓毒症 SA-AKI 的曲线下面积(AUC)分别为 0.896 和 0.814。miR-370-3p 和 miR-495-3p 表达较高的患者 28 天生存率较高。

结论

miR-370-3p 和 miR-495-3p 可能是 SA-AKI 的早期诊断的新型生物标志物,在 SA-AKI 患者的尿液中明显降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/f8166a1e9ef0/CMMM2022-2439509.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/ccabe4157d69/CMMM2022-2439509.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/93f5628c5c54/CMMM2022-2439509.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/f8166a1e9ef0/CMMM2022-2439509.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/ccabe4157d69/CMMM2022-2439509.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/93f5628c5c54/CMMM2022-2439509.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d281/9293507/f8166a1e9ef0/CMMM2022-2439509.003.jpg

相似文献

1
The Potential of miR-370-3p and miR-495-3p Serving as Biomarkers for Sepsis-Associated Acute Kidney Injury.miR-370-3p 和 miR-495-3p 作为脓毒症相关性急性肾损伤生物标志物的潜力。
Comput Math Methods Med. 2022 Jul 11;2022:2439509. doi: 10.1155/2022/2439509. eCollection 2022.
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
[Value of serum miR-21-3p in predicting acute kidney injury in children with sepsis].血清miR-21-3p在预测脓毒症患儿急性肾损伤中的价值
Zhongguo Dang Dai Er Ke Za Zhi. 2020 Mar;22(3):269-273. doi: 10.7499/j.issn.1008-8830.2020.03.016.
4
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.
5
Plasma-derived exosomal hsa-miR-184 and hsa-mir-6766-3p as promising diagnostic biomarkers for early detection of children's cardiac surgery-associated acute kidney injury.血浆衍生的外泌体 hsa-miR-184 和 hsa-mir-6766-3p 作为儿童心脏手术相关急性肾损伤早期检测的有前途的诊断生物标志物。
Sci Rep. 2024 Sep 27;14(1):22387. doi: 10.1038/s41598-024-72737-w.
6
Sepsis-Associated Acute Kidney Injury: Where Are We Now?脓毒症相关性急性肾损伤:我们现在在哪里?
Medicina (Kaunas). 2024 Mar 6;60(3):434. doi: 10.3390/medicina60030434.
7
Diagnostic and prognostic significance of aberrant miR-652-3p levels in patients with acute decompensated heart failure and acute kidney injury.急性失代偿性心力衰竭和急性肾损伤患者中异常miR-652-3p水平的诊断和预后意义
J Int Med Res. 2020 Nov;48(11):300060520967829. doi: 10.1177/0300060520967829.
8
Urinary miR-26b as a potential biomarker for patients with sepsis-associated acute kidney injury: a Chinese population-based study.基于中国人群的研究:尿 miR-26b 作为脓毒症相关急性肾损伤患者的潜在生物标志物。
Eur Rev Med Pharmacol Sci. 2018 Jul;22(14):4604-4610. doi: 10.26355/eurrev_201807_15518.
9
A Pilot Study Identifying a Set of microRNAs As Precise Diagnostic Biomarkers of Acute Kidney Injury.一项确定一组微小RNA作为急性肾损伤精确诊断生物标志物的初步研究。
PLoS One. 2015 Jun 16;10(6):e0127175. doi: 10.1371/journal.pone.0127175. eCollection 2015.
10
Circ-BNIP3L knockdown alleviates LPS-induced renal tubular epithelial cell injury during sepsis-associated acute kidney injury by miR-370-3p/MYD88 axis.环状 RNA-BNIP3L 敲低通过 miR-370-3p/MYD88 轴减轻脓毒症相关急性肾损伤时脂多糖诱导的肾小管上皮细胞损伤。
J Bioenerg Biomembr. 2021 Dec;53(6):665-677. doi: 10.1007/s10863-021-09925-0. Epub 2021 Nov 3.

引用本文的文献

1
miR-370-3p affects the progression of postmenopausal osteoporosis through targeting INO80.微小RNA-370-3p通过靶向INO80影响绝经后骨质疏松症的进展。
Hereditas. 2025 Jul 22;162(1):138. doi: 10.1186/s41065-025-00502-8.
2
LEF1 influences diabetic retinopathy and retinal pigment epithelial cell ferroptosis the axis through .LEF1通过……轴影响糖尿病性视网膜病变和视网膜色素上皮细胞铁死亡。
World J Diabetes. 2025 Mar 15;16(3):92003. doi: 10.4239/wjd.v16.i3.92003.
3
A Systematic Review and Meta-Analysis of MicroRNA as Predictive Biomarkers of Acute Kidney Injury.

本文引用的文献

1
Circ-BNIP3L knockdown alleviates LPS-induced renal tubular epithelial cell injury during sepsis-associated acute kidney injury by miR-370-3p/MYD88 axis.环状 RNA-BNIP3L 敲低通过 miR-370-3p/MYD88 轴减轻脓毒症相关急性肾损伤时脂多糖诱导的肾小管上皮细胞损伤。
J Bioenerg Biomembr. 2021 Dec;53(6):665-677. doi: 10.1007/s10863-021-09925-0. Epub 2021 Nov 3.
2
Risk factors, clinical features and outcome of new-onset acute kidney injury among critically ill patients: a database analysis based on prospective cohort study.危重症患者新发急性肾损伤的危险因素、临床特征及转归:基于前瞻性队列研究的数据库分析。
BMC Nephrol. 2021 Aug 25;22(1):289. doi: 10.1186/s12882-021-02503-x.
3
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.
4
Sepsis-Associated Acute Kidney Injury: Where Are We Now?脓毒症相关性急性肾损伤:我们现在在哪里?
Medicina (Kaunas). 2024 Mar 6;60(3):434. doi: 10.3390/medicina60030434.
5
Kidney Injury: Focus on Molecular Signaling Pathways.肾脏损伤:聚焦分子信号通路。
Curr Med Chem. 2024;31(28):4510-4533. doi: 10.2174/0109298673271547231108060805.
miR‑214 ameliorates sepsis‑induced acute kidney injury via PTEN/AKT/mTOR‑regulated autophagy.
miR-214 通过调控 PTEN/AKT/mTOR 通路改善脓毒症诱导的急性肾损伤。
Mol Med Rep. 2021 Oct;24(4). doi: 10.3892/mmr.2021.12322. Epub 2021 Jul 30.
4
Elevated Serum and Urine MiR-429 Contributes to the Progression of Gestational Diabetes Mellitus.血清和尿液中 miR-429 水平升高促进妊娠期糖尿病的进展。
Clin Lab. 2021 May 1;67(5). doi: 10.7754/Clin.Lab.2020.200909.
5
Exosomal miR-125b-5p deriving from mesenchymal stem cells promotes tubular repair by suppression of p53 in ischemic acute kidney injury.源自间充质干细胞的外泌体miR-125b-5p通过抑制缺血性急性肾损伤中的p53促进肾小管修复。
Theranostics. 2021 Mar 11;11(11):5248-5266. doi: 10.7150/thno.54550. eCollection 2021.
6
Long non-coding RNA SNHG14 aggravates LPS-induced acute kidney injury through regulating miR-495-3p/HIPK1.长链非编码 RNA SNHG14 通过调节 miR-495-3p/HIPK1 加重 LPS 诱导的急性肾损伤。
Acta Biochim Biophys Sin (Shanghai). 2021 May 21;53(6):719-728. doi: 10.1093/abbs/gmab034.
7
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.
8
Acute Kidney Injury in Sepsis: Evidence From Asia.脓毒症相关性急性肾损伤:来自亚洲的证据。
Semin Nephrol. 2020 Sep;40(5):489-497. doi: 10.1016/j.semnephrol.2020.08.005.
9
Discovery and validation of miR-452 as an effective biomarker for acute kidney injury in sepsis.发现并验证 miR-452 作为脓毒症急性肾损伤的有效生物标志物。
Theranostics. 2020 Oct 25;10(26):11963-11975. doi: 10.7150/thno.50093. eCollection 2020.
10
miR-30c-5p Alleviated Pyroptosis During Sepsis-Induced Acute Kidney Injury via Targeting TXNIP.miR-30c-5p 通过靶向 TXNIP 减轻脓毒症诱导的急性肾损伤中的细胞焦亡。
Inflammation. 2021 Feb;44(1):217-228. doi: 10.1007/s10753-020-01323-9.