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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。

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.

机构信息

Department of Nephrology, The Affiliated Hospital of Qingdao University, No. 16, Jiangsu Road, Qingdao, 266003, Shandong, China.

Department of Respiratory and Critical Care Medicine, The Affiliated Hospital of Qingdao University, No. 16, Jiangsu Road, Qingdao, 266003, Shandong, China.

出版信息

Int Urol Nephrol. 2021 Oct;53(10):2107-2116. doi: 10.1007/s11255-021-02784-z. Epub 2021 Jan 28.


DOI:10.1007/s11255-021-02784-z
PMID:33511504
Abstract

BACKGROUND: Acute kidney injury (AKI) is a common and serious complication of sepsis. MicroRNA-22-3p (miR-22-3p) has been found to be involved in septic AKI progression. The purpose of this study was to analyze both the serum and urinary expression of miR-22-3p in septic AKI patients, and evaluated the clinical value of miR-22-3p in the diagnosis and prognosis of sepsis-induced AKI. METHODS: Serum and urinary expression of miR-22-3p was examined using qRT-PCR. The risk factors related with septic AKI onset were assessed using logistic analysis. A receiver-operating characteristic (ROC) curve was constructed to evaluate the diagnostic performance of miR-22-3p, and the Kaplan-Meier survival curves and Cox regression analysis were used to evaluate the predictive value of miR-22-3p for the 28-day survival of septic AKI patients. RESULTS: Both serum and urinary miR-22-3p expression was decreased and negatively correlated with kidney injury biomarkers in septic AKI patients. MiR-22-3p expression was a risk factor for AKI onset and had diagnostic accuracy in septic AKI patients. The expression of both serum and urinary miR-22-3p was lower in patients who died, and served as a prognostic biomarker to predict 28-day survival in septic AKI patients. CONCLUSION: Serum and urinary miR-22-3p was reduced in sepsis-induced AKI patients, and served as a biomarker to predict AKI occurrence and 28-day survival in sepsis patients.

摘要

背景:急性肾损伤(AKI)是脓毒症的常见且严重的并发症。已经发现 microRNA-22-3p(miR-22-3p)参与了脓毒症 AKI 的进展。本研究旨在分析脓毒症 AKI 患者血清和尿液中 miR-22-3p 的表达,并评估 miR-22-3p 在诊断和预测脓毒症诱导的 AKI 方面的临床价值。

方法:采用 qRT-PCR 检测 miR-22-3p 的血清和尿液表达。使用逻辑回归分析评估与脓毒症 AKI 发病相关的危险因素。构建受试者工作特征(ROC)曲线评估 miR-22-3p 的诊断性能,Kaplan-Meier 生存曲线和 Cox 回归分析用于评估 miR-22-3p 对脓毒症 AKI 患者 28 天生存率的预测价值。

结果:脓毒症 AKI 患者血清和尿液 miR-22-3p 的表达均降低,与肾损伤生物标志物呈负相关。miR-22-3p 表达是 AKI 发病的危险因素,对脓毒症 AKI 患者具有诊断准确性。死亡患者的血清和尿液 miR-22-3p 表达均较低,是预测脓毒症 AKI 患者 28 天生存率的预后生物标志物。

结论:脓毒症诱导的 AKI 患者血清和尿液中 miR-22-3p 减少,可作为预测 AKI 发生和脓毒症患者 28 天生存率的生物标志物。

相似文献

[1]
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.

Int Urol Nephrol. 2021-10

[2]
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[3]
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[4]
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[5]
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Int Urol Nephrol. 2024-5

[6]
Urinary miR-26b as a potential biomarker for patients with sepsis-associated acute kidney injury: a Chinese population-based study.

Eur Rev Med Pharmacol Sci. 2018-7

[7]
The Potential of miR-370-3p and miR-495-3p Serving as Biomarkers for Sepsis-Associated Acute Kidney Injury.

Comput Math Methods Med. 2022

[8]
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.

Bosn J Basic Med Sci. 2019-8-20

[9]
Clinical value of serum miR-320-3p expression in predicting the prognosis of sepsis-induced acute kidney injury.

J Clin Lab Anal. 2022-5

[10]
[Predictive value of miRNA-29a and miRNA-10a-5p for 28-day mortality in patients with sepsis-induced acute kidney injury].

Nan Fang Yi Ke Da Xue Xue Bao. 2017-5-20

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.

Front Mol Biosci. 2025-8-7

[2]
Analysis of the diagnostic and prognostic value of Peripheral blood mononuclear cell microRNA-9-5p in patients with sepsis in the intensive care unit.

Front Cell Infect Microbiol. 2025-4-22

[3]
Unveiling the Therapeutic Potential of Dulaglutide in Mitigating Tacrolimus-Induced Nephrotoxicity Through Targeting the miR-22/HMGB-1/TLR4/MyD88/NF-κB Trajectory.

Arch Pharm (Weinheim). 2025-4

[4]
The Role of MicroRNA in the Pathogenesis of Acute Kidney Injury.

Cells. 2024-9-16

[5]
Sepsis Biomarkers: Advancements and Clinical Applications-A Narrative Review.

Int J Mol Sci. 2024-8-19

[6]
A Systematic Review and Meta-Analysis of MicroRNA as Predictive Biomarkers of Acute Kidney Injury.

Biomedicines. 2024-7-30

[7]
Evaluation of urinary neutrophil gelatinase associated lipocalin in the early diagnosis of acute kidney injury with sepsis.

Am J Transl Res. 2024-4-15

[8]
Machine learning for prediction of acute kidney injury in patients diagnosed with sepsis in critical care.

PLoS One. 2024

[9]
Knockdown of circ-Gatad1 alleviates LPS induced HK2 cell injury via targeting miR-22-3p/TRPM7 axis in septic acute kidney.

BMC Nephrol. 2024-3-5

[10]
MicroRNAs as Biomarkers and Therapeutic Targets for Acute Kidney Injury.

Diagnostics (Basel). 2023-9-9

本文引用的文献

[1]
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Zhongguo Dang Dai Er Ke Za Zhi. 2020-3

[2]
Study of MicroRNA-122 as a Diagnostic Biomarker of Sepsis.

Egypt J Immunol. 2019-7

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A functional polymorphism rs10830963 in melatonin receptor 1B associated with the risk of gestational diabetes mellitus.

Biosci Rep. 2019-12-20

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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.

Bosn J Basic Med Sci. 2019-8-20

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Oncol Lett. 2018-10

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Urinary miR-26b as a potential biomarker for patients with sepsis-associated acute kidney injury: a Chinese population-based study.

Eur Rev Med Pharmacol Sci. 2018-7

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[Predictive value of miRNA-29a and miRNA-10a-5p for 28-day mortality in patients with sepsis-induced acute kidney injury].

Nan Fang Yi Ke Da Xue Xue Bao. 2017-5-20

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