临床医学论著

血浆MicroRNA-296-5P、MicroRNA-107表达水平对急性心肌梗死诊断的预测价值*

  • 赵强 ,
  • 赵瑞平
展开
  • 1.内蒙古科技大学包头医学院中心临床医学院,内蒙古包头 014040;
    2.包头市中心医院

收稿日期: 2023-08-26

  网络出版日期: 2023-12-18

基金资助

*包头医学院研究生科研创新项目(bycx2021025)

Predictive value of plasma MicroRNA-296-5P and MicroRNA-107 expression levels in the diagnosis of acute myocardial infarction

  • ZHAO Qiang ,
  • ZHAO Ruiping
Expand
  • 1. Center Clinical Medical School, Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou 014040,China;
    2. Baotou Centeral Hospital

Received date: 2023-08-26

  Online published: 2023-12-18

摘要

目的: 通过检测急性心肌梗死患者、健康人群血浆中miR-296-5p、miR-107表达水平及在急性心肌梗死患者体内时间变化趋势,探讨其作为急性心肌梗死诊断标志物的可能性。方法: 选取2021年11月—2022年3月间在包头市中心医院心内科就诊急性心肌梗死患者60例(心梗组)和同时期在体检中心体检的年龄相匹配的健康就诊者60例(对照组)。心梗组根据采取干预措施不同分为再灌注组30例,常规药物治疗30例。应用荧光定量实时PCR技术(RT-qPCR)检测入院时及采取干预措施后不同时间段血浆miR-296-5p、miR-107的相对表达量。结果: 与对照组相比,急性心肌梗死患者血浆miR-296-5p、miR-107表达量显著升高(P<0.05)。经再灌注治疗或常规药物治疗48 h后,血浆miR-296-5p、miR-107相对表达量明显降低(P<0.05)。经再灌注治疗或常规药物治疗7 d后,血浆miR-296-5p、miR-107相对表达量降至正常人水平(P<0.05)。结论: 急性心肌梗死患者血浆miR-296-5p、miR-107相对表达含量较正常人显著升高,在采取干预措施后呈下降趋势,对急性心肌梗死的诊断有预测价值。

本文引用格式

赵强 , 赵瑞平 . 血浆MicroRNA-296-5P、MicroRNA-107表达水平对急性心肌梗死诊断的预测价值*[J]. 包头医学院学报, 2023 , 39(12) : 36 -39 . DOI: 10.16833/j.cnki.jbmc.2023.12.007

Abstract

Objective: To explore the possibility of miR-296-5p and miR-107 as diagnostic markers of acute myocardial infarction by detecting the expression levels of miR-296-5p and miR-107 in plasma of patients with acute myocardial infarction and healthy people and the time trend in patients with acute myocardial infarction. Methods: From November 2021 to March 2022, 60 patients with acute myocardial infarction (myocardial infarction group) and 60 age-matched healthy patients (control group) who underwent physical examination in the physical examination center of Baotou Central Hospital were selected as the research objects. The myocardial infarction group was divided into reperfusion group (30 patients) and conventional drug treatment group (30 patients) according to different intervention measures. Fluorescence quantitative real-time PCR (RT-qPCR) was used to detect the relative expression of plasma miR-296-5p and miR-107 at admission and at different time points after intervention. Results: Compared with the control group, the expression levels of plasma miR-296-5p and miR-107 in patients with acute myocardial infarction were significantly increased (P<0.05). After 48 hours of reperfusion therapy or conventional drug treatment, the relative expression levels of plasma miR-296-5p and miR-107 were significantly decreased (P<0.05). After 7 days of reperfusion therapy or conventional drug treatment, the relative expression of plasma miR-296-5p and miR-107 decreased to normal levels (P<0.05). Conclusion: The relative expression levels of miR-296-5p and miR-107 in plasma of patients with acute myocardial infarction are significantly higher than those of normal individuals, and shows a downward trend after intervention measures, which has predictive value for the diagnosis of acute myocardial infarction.

参考文献

[1] 国家卫生健康委员会. 中国卫生健康统计年鉴-2021[M]. 北京:中国协和医科大学出版社,2021.
[2] Hatzistergos KE,Quevedo H,Oskouei BN,et al. Bone marrow mesenchymal stem cells stimulate cardiac stem cell proliferation and differentiation[J]. Circulation Research, 2010, 107(7):913-922.
[3] Mayorga ME,Dong F,Sundararaman S,et al. Central role for disabled-2 in mesenchymal stem cardiac protein expression and functional consequences after engraftment in acute myocardial infarction[J]. Stem Cells Dev, 2011, 20(4):681-693.
[4] Thygesen K,Alpert JS,Jaffe AS,et al.Fourth universal definition of myocardial infarction(2018)[J].Eur Heart J,2018,00(0):00-00.
[5] Kozomara A, Griffiths-Jones S. miRBase: integrating microRNA annotation and deep-sequencing data[J]. Nucleic Acids Res, 2011,39(Database issue):D152-D157.
[6] Norcini M, Sideris A, Martin Hernandez LA, et al. An approach to identify microRNAs involved in neuropathic pain following a peripheral nerve injury[J]. Front Neurosci,2014,8:266.
[7] Kim GH.MicroRNA regulation of cardiac conduction and arrhythmias[J]. Transl Res,2013, 161(5):381-392.
[8] Frankel LB,Lund AH.MicroRNA regulation of autophagy[J]. Carcinogenesis, 2012, 33(11):2018-2025.
[9] Xiao J, Liang D,Zhang H,et al. MicroRNA-204 is required for differentiation of human-derived cardiomyocyte progenitor cells[J]. J Mol Cell Cardiol,2012,53(6):751-759.
[10] Rognoni A,Cavallino C,Lupi A,et al. Novel biomarkers in the diagnosis of acute coronary syndromes: the role of circulating miRNAs[J]. Expert Rev Cardiovasc Ther, 2014, 12(9):1119-1124.
[11] Sayed ASM,Xia K,Salma U,et al. Diagnosis, prognosis and therapeutic role of circulating miRNAs in cardiovascular diseases[J]. Heart Lung Circ, 2014, 23(6):503-510.
[12] Li J,Xu J,Cheng Y,et al. Circulating microRNAs as mirrors of acute coronary syndromes: MiRacle or quagMire[J]. J Cell Mol Med, 2013, 17(11):1363-1370.
[13] Song Y, Zhang C, Zhang J, et al. Localized injection of miR-21-enriched extracellular vesicles effectively restores cardiac function after myocardial infarction[J]. Theranostics, 2019,9(8):2346-2360.
[14] Liu H, Zhang Y, Yuan J, et al. Dendritic cellderived exosomal miR4943p promotes angiogenesis following myocardial infarction[J]. Int J Mol Med, 2021,47(1):315-325.
[15] Qu Y, Zhang J, Zhang J, et al. MiR-708-3p alleviates inflammation and myocardial injury after myocardial infarction by suppressing ADAM17 expression[J]. Inflammation, 2021,44(3):1083-1095.
文章导航

/