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miR-139-5p在急性冠状动脉综合征中的临床意义及其对急性冠状动脉综合征进展的潜在影响。

The Clinical Significance of miR-139-5p in Acute Coronary Syndrome and its Potential Effect on the Progression of Acute Coronary Syndrome.

作者信息

Wang Zhe, Ma Qiaoli, Lin Fei

机构信息

Department of Cardiology, Zibo First Hospital, No.121, Nanjing Road, Shandong, 255022, Zhangdian District, China.

Department of Cardiology, Zibo Central Hospital, Shandong, 255090, China.

出版信息

J Cardiovasc Transl Res. 2025 May 29. doi: 10.1007/s12265-025-10625-y.

DOI:10.1007/s12265-025-10625-y
PMID:40439867
Abstract

To investigate the role of miR-139-5p in acute coronary syndrome (ACS), serum miR-139-5p levels were measured via quantitative real-time polymerase chain reaction (qRT-PCR) in 117 ACS patients, 91 stable angina (SAP) patients, 89 healthy controls. Its associations with ACS severity, major adverse cardiovascular events (MACE) were evaluated using statistical tests, Kaplan-Meier survival, COX regression analysis. Effect of miR-139-5p on cell function and inflammation in oxidized low-density lipoprotein (ox-LDL) -induced human coronary artery smooth muscle cells (HCASMCs) was evaluated in vitro. Upregulated miR-134-5p in ACS distinguished ACS from SAP/health individuals, correlating with increased cardiac troponin I (cTnI), Gensini score, MACE risk. COX regression identified miR-139-5p as independent ACS prognostic factors. In vitro, miR-139-5p downregulation suppressed ox-LDL-induced HCASMC proliferation, migration, and inflammation. Upregulated miR-139-5p expression showed a diagnostic and prognostic value on ACS and was correlated with ACS severity. Downregulated miR-139-5p expression exhibited a suppressive effect on ACS progression.

摘要

为研究miR-139-5p在急性冠状动脉综合征(ACS)中的作用,采用定量实时聚合酶链反应(qRT-PCR)检测了117例ACS患者、91例稳定型心绞痛(SAP)患者及89例健康对照者的血清miR-139-5p水平。运用统计学检验、Kaplan-Meier生存分析及COX回归分析评估其与ACS严重程度、主要不良心血管事件(MACE)的相关性。体外评估miR-139-5p对氧化型低密度脂蛋白(ox-LDL)诱导的人冠状动脉平滑肌细胞(HCASMCs)细胞功能和炎症的影响。ACS中上调的miR-134-5p可将ACS与SAP/健康个体区分开来,与心肌肌钙蛋白I(cTnI)升高、Gensini评分及MACE风险相关。COX回归分析确定miR-139-5p为ACS独立的预后因素。在体外,下调miR-139-5p可抑制ox-LDL诱导的HCASMC增殖、迁移及炎症反应。上调的miR-139-5p表达对ACS具有诊断和预后价值,并与ACS严重程度相关。下调的miR-139-5p表达对ACS进展具有抑制作用。

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本文引用的文献

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Genome-wide DNA methylation profiling in blood reveals epigenetic signature of incident acute coronary syndrome.全基因组 DNA 甲基化谱在血液中揭示了急性冠状动脉综合征发病的表观遗传特征。
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miR-223-5p serves as a diagnostic biomarker for acute coronary syndrome and its predictive value for the clinical outcome after PCI.miR-223-5p 可作为急性冠状动脉综合征的诊断生物标志物及其对 PCI 后临床结局的预测价值。
BMC Cardiovasc Disord. 2024 Aug 13;24(1):423. doi: 10.1186/s12872-024-04088-3.
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Circulating mir-483-5p as a novel diagnostic biomarker for acute coronary syndrome and its predictive value for the clinical outcome after PCI.
循环 mir-483-5p 作为急性冠状动脉综合征的新型诊断生物标志物及其对 PCI 后临床结局的预测价值。
BMC Cardiovasc Disord. 2023 Jul 18;23(1):360. doi: 10.1186/s12872-023-03387-5.
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Di-n-butyl phthalate regulates vascular smooth muscle cells phenotypic switching by MiR-139-5p-MYOCD pathways.邻苯二甲酸二正丁酯通过 miR-139-5p-MYOCD 通路调节血管平滑肌细胞表型转换。
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