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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。

Clinical value of microRNA-378a-3p in sepsis and its role in sepsis-induced inflammation and cardiac dysfunction.

机构信息

Department Of Emergency, Emergency General Hospital, Beijing, China.

出版信息

Bioengineered. 2021 Dec;12(1):8496-8504. doi: 10.1080/21655979.2021.1985339.

DOI:10.1080/21655979.2021.1985339
PMID:34565302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8806767/
Abstract

This study explored the clinical meaning of miR-378a-3p in sepsis and its influence on sepsis-induced inflammation and cardiac dysfunction. Serum levels of miR-378a-3p were detected by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR). The Receiver Operating Characteristic (ROC) curve was used to evaluate its diagnostic value. The effects of miR-378a-3p on inflammation and cardiac function were evaluated by monitoring left ventricular systolic pressure (LVSP), left ventricular and end-diastolic pressure (LVEDP), maximum rate of change in left ventricular pressure (± dp/dt) and detecting the levels of troponin I (cTnI), creatine kinase isoenzyme MB (CK-MB), tumor necrosis factor-a (TNF-a), interleukin-6 (IL-6), and interleukin-1β (IL-1β) via enzyme linked immunosorbent assay (ELISA). Serum miR-378a-3p was increased in sepsis patients and rat model. ROC curve indicated that miR-378a-3p might have diagnostic significance for sepsis miR-378a-3p antagomir improved the cardiac function by upregulating the levels of LVSP and ± dp/dt, and decreasing the levels of LVEDP, cTnI and CK-MB in rat model. miR-378a-3p antagomir also significantly alleviated the inflammatory responseby down-regulating the expression of TNF-a, IL-6, and IL-1β. Besides, logistics regression analysis illustrated that miR-378a-3p was an independent influencing factor for the onset of cardiac dysfunction in sepsis. miR-378a-3p has the potential as a diagnostic biomarker for sepsis and decreasing the level of miR-378a-3p had the ability to ameliorate cardiac dysfunction and inflammatory response caused by sepsis.

摘要

本研究探讨了 miR-378a-3p 在脓毒症中的临床意义及其对脓毒症引起的炎症和心功能障碍的影响。通过定量实时聚合酶链反应 (qRT-PCR) 检测血清 miR-378a-3p 水平。采用受试者工作特征 (ROC) 曲线评估其诊断价值。通过监测左心室收缩压 (LVSP)、左心室和舒张末期压 (LVEDP)、左心室压力最大变化率 (± dp/dt),以及通过酶联免疫吸附试验 (ELISA) 检测肌钙蛋白 I (cTnI)、肌酸激酶同工酶 MB (CK-MB)、肿瘤坏死因子-a (TNF-a)、白细胞介素-6 (IL-6) 和白细胞介素-1β (IL-1β) 的水平,评估 miR-378a-3p 对炎症和心功能的影响。脓毒症患者和大鼠模型中血清 miR-378a-3p 增加。ROC 曲线表明,miR-378a-3p 可能对脓毒症具有诊断意义。miR-378a-3p 拮抗剂通过上调 LVSP 和 ± dp/dt 的水平,降低 LVEDP、cTnI 和 CK-MB 的水平,改善了大鼠模型的心功能。miR-378a-3p 拮抗剂还通过下调 TNF-a、IL-6 和 IL-1β 的表达,显著缓解了炎症反应。此外,逻辑回归分析表明,miR-378a-3p 是脓毒症心功能障碍发生的独立影响因素。miR-378a-3p 具有作为脓毒症诊断生物标志物的潜力,降低 miR-378a-3p 的水平具有改善脓毒症引起的心功能障碍和炎症反应的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/20906aa26264/KBIE_A_1985339_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/3e88c78f880f/KBIE_A_1985339_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/517b977da790/KBIE_A_1985339_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/de01f083f136/KBIE_A_1985339_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/20906aa26264/KBIE_A_1985339_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/3e88c78f880f/KBIE_A_1985339_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/517b977da790/KBIE_A_1985339_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/de01f083f136/KBIE_A_1985339_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c4/8806767/20906aa26264/KBIE_A_1985339_F0004_B.jpg

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