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Circulating microRNA in cardiovascular disease.循环 microRNA 在心血管疾病中的作用。
Adv Clin Chem. 2019;91:99-122. doi: 10.1016/bs.acc.2019.03.003. Epub 2019 Apr 24.
2
Fourth Universal Definition of Myocardial Infarction (2018).心肌梗死的第四次全球定义(2018年)。
Circulation. 2018 Nov 13;138(20):e618-e651. doi: 10.1161/CIR.0000000000000617.
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2018 ESC/EACTS Guidelines on myocardial revascularization.2018年欧洲心脏病学会/欧洲心胸外科学会心肌血运重建指南。
Eur Heart J. 2019 Jan 7;40(2):87-165. doi: 10.1093/eurheartj/ehy394.
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Advances in Coronary No-Reflow Phenomenon-a Contemporary Review.冠状动脉无复流现象的研究进展——当代综述
Curr Atheroscler Rep. 2018 Jul 5;20(9):44. doi: 10.1007/s11883-018-0747-5.
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Non-coding RNAs as biomarkers for acute myocardial infarction.非编码 RNA 作为急性心肌梗死的生物标志物。
Acta Pharmacol Sin. 2018 Jul;39(7):1110-1119. doi: 10.1038/aps.2017.205. Epub 2018 Apr 26.
6
2017 ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation: The Task Force for the management of acute myocardial infarction in patients presenting with ST-segment elevation of the European Society of Cardiology (ESC).2017年欧洲心脏病学会(ESC)ST段抬高型急性心肌梗死患者管理指南:欧洲心脏病学会(ESC)ST段抬高型急性心肌梗死患者管理工作组
Eur Heart J. 2018 Jan 7;39(2):119-177. doi: 10.1093/eurheartj/ehx393.
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40 years of percutaneous coronary intervention: where next?经皮冠状动脉介入治疗40年:未来何去何从?
Lancet. 2017 Aug 19;390(10096):715. doi: 10.1016/S0140-6736(17)32238-9.
8
Profiling and validation of circulating microRNAs for cardiovascular events in patients presenting with ST-segment elevation myocardial infarction.ST 段抬高型心肌梗死患者心血管事件相关循环 microRNAs 的分析与验证。
Eur Heart J. 2017 Feb 14;38(7):511-515. doi: 10.1093/eurheartj/ehw563.
9
Circulating microRNAs predict future fatal myocardial infarction in healthy individuals - The HUNT study.循环微RNA可预测健康个体未来的致命性心肌梗死——HUNT研究
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10
ST-segment elevation myocardial infarction in China from 2001 to 2011 (the China PEACE-Retrospective Acute Myocardial Infarction Study): a retrospective analysis of hospital data.2001年至2011年中国ST段抬高型心肌梗死(中国PEACE-急性心肌梗死回顾性研究):医院数据的回顾性分析
Lancet. 2015 Jan 31;385(9966):441-51. doi: 10.1016/S0140-6736(14)60921-1. Epub 2014 Jun 23.

循环 miR-660-5p 与行直接经皮冠状动脉介入治疗的 ST 段抬高型心肌梗死患者无复流现象相关。

Circulating miR-660-5p is associated with no-reflow phenomenon in patients with ST segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.

机构信息

Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University; Beijing-China.

Department of Outpatient, Beijing Friendship Hospital, Capital Medical University; Beijing-China.

出版信息

Anatol J Cardiol. 2021 May;25(5):323-329. doi: 10.14744/AnatolJCardiol.2020.29267.

DOI:10.14744/AnatolJCardiol.2020.29267
PMID:33960307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8114630/
Abstract

OBJECTIVE

This study aims to investigate the association of circulating miR-660-5p with no-reflow phenomenon (NRP) in patients with ST segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI).

METHODS

Consecutive patients diagnosed with anterior STEMI within 12 h of pain onset were included; in these patients, coronary angiography confirmed that the left anterior descending artery was infarcted. Angiographic NRP was defined as a final thrombolysis in myocardial infarction (TIMI) flow 2 or 3 with a myocardial blush grade (MBG) <2. High miR-660-5p was defined as a value in the third tertile. The relationship of circulating miR-660-5p with NRP was assessed using Spearman correlation analysis and multiple logistic regression analysis.

RESULTS

Fifty-two eligible patients were finally included in this study (mean age: 56±12.4 years, >65 years: 53.8%, male: 76.9%, and mean Body Mass Index: 26.3±3.5). The incidence of NRP was 38.5%. Circulating miR-660-5p was significantly related to the mean platelet volume (MPV). The patients were grouped into tertiles by miR-660-5p levels (Q1: <7.18, Q2: 7.18-11.31, Q3: >11.31). Those in the high microRNA-660-5p group had nearly a 6-fold higher risk of NRP than those in the low microRNA-660-5p group [odds ratio (OR) = 5.68, 95% confidence interval (CI) 1.40-23.07, p=0.015]. When analyzed by tertiles, relative odds of NRP were consistently increasing (OR1 for Q2 vs. Q1: 1.25, 95% CI: 0.27-5.73, p=0.770; OR2 for Q3 vs. Q1: 5.96, 95% CI: 1.33-26.66, p=0.02), despite multivariable adjustment. Receiver operating characteristic curve analysis demonstrated that the microRNA-660-5p level of 10.17 was the best cut-off level to predict the incidence of the NRP in patients undergoing PPCI with an area under the ROC curve (AUC) of 0.768 (95% CI: 0.636-0.890).

CONCLUSION

Circulating miR-660-5p was significantly associated with NRP, and it may be a useful biomarker to predict the incidence of NRP in patients with STEMI undergoing PPCI.

摘要

目的

本研究旨在探讨循环 miR-660-5p 与接受直接经皮冠状动脉介入治疗(PPCI)的 ST 段抬高型心肌梗死(STEMI)患者无复流现象(NRP)之间的关系。

方法

纳入胸痛发作后 12 小时内确诊为前壁 STEMI 的连续患者;这些患者的冠状动脉造影证实左前降支梗死。血管造影 NRP 定义为最终血栓溶解心肌梗死(TIMI)血流 2 或 3 级,心肌灌注分级(MBG)<2。高 miR-660-5p 定义为第 3 个三分位值。采用 Spearman 相关分析和多因素 logistic 回归分析评估循环 miR-660-5p 与 NRP 的关系。

结果

本研究最终纳入 52 例符合条件的患者(平均年龄:56±12.4 岁,>65 岁:53.8%,男性:76.9%,平均体重指数:26.3±3.5)。NRP 的发生率为 38.5%。循环 miR-660-5p 与平均血小板体积(MPV)显著相关。根据 miR-660-5p 水平将患者分为三分位组(Q1:<7.18,Q2:7.18-11.31,Q3:>11.31)。高 microRNA-660-5p 组的 NRP 风险几乎是低 microRNA-660-5p 组的 6 倍[优势比(OR)=5.68,95%置信区间(CI)1.40-23.07,p=0.015]。按三分位分析,NRP 的相对优势比持续增加(OR1 与 Q2 相比 Q1:1.25,95%CI:0.27-5.73,p=0.770;OR2 与 Q3 相比 Q1:5.96,95%CI:1.33-26.66,p=0.02),尽管进行了多变量调整。受试者工作特征曲线分析表明,miR-660-5p 水平为 10.17 是预测行 PPCI 的 STEMI 患者 NRP 发生率的最佳截断值,ROC 曲线下面积(AUC)为 0.768(95%CI:0.636-0.890)。

结论

循环 miR-660-5p 与 NRP 显著相关,可能是预测 STEMI 患者行 PPCI 后 NRP 发生率的有用生物标志物。