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miR-223 和 miR-186 与心肌梗死后的长期死亡率相关。

MiR-223 and MiR-186 Are Associated with Long-Term Mortality after Myocardial Infarction.

机构信息

Department of Cardiology, Rangueil University Hospital, 31400 Toulouse, France.

Center for Clinical Investigation (CIC1436)/CARDIOMET, Rangueil University Hospital, 31400 Toulouse, France.

出版信息

Biomolecules. 2022 Sep 6;12(9):1243. doi: 10.3390/biom12091243.

DOI:10.3390/biom12091243
PMID:36139082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9496068/
Abstract

Background-The identification and stratification of patients at risk of fatal outcomes after myocardial infarction (MI) is of considerable interest to guide secondary prevention therapies. Currently, no accurate biomarkers are available to identify subjects who are at risk of suffering acute manifestations of coronary heart disease as well as to predict adverse events after MI. Non-coding circulating microRNAs (miRNAs) have been proposed as novel diagnostic and prognostic biomarkers in cardiovascular diseases. The aims of the study were to investigate the clinical value of a panel of circulating miRNAs as accurate biomarkers associated with MI and mortality risk prediction in patients with documented MI. Methods and Results-seven circulating plasma miRNAs were analyzed in 67 MI patients and 80 control subjects at a high cardiovascular risk but without known coronary diseases. Multivariate logistic regression analyses demonstrated that six miRNAs were independently associated with MI occurrence. Among them, miR-223 and miR-186 reliably predicted long-term mortality in MI patients, in particular miR-223 (HR 1.57 per one-unit increase, = 0.02), after left ventricular ejection fraction (LVEF) adjustment. Kaplan-Meier survival analyses provided a predictive threshold value of miR-223 expression ( = 0.028) for long-term mortality. Conclusions-Circulating miR-223 and miR-186 are promising predictive biomarkers for long-term mortality after MI.

摘要

背景-鉴定和分层心肌梗死后(MI)发生致命后果的患者对于指导二级预防治疗具有重要意义。目前,尚无准确的生物标志物可用于识别有发生冠心病急性表现风险的患者,并预测 MI 后的不良事件。非编码循环 microRNAs(miRNAs)已被提出作为心血管疾病的新型诊断和预后生物标志物。本研究旨在探讨一组循环 miRNAs 作为与 MI 相关的准确生物标志物的临床价值,并预测有记录 MI 的患者的死亡风险。

方法和结果-在 67 例 MI 患者和 80 例高心血管风险但无已知冠心病的对照受试者中分析了 7 种循环血浆 miRNA。多变量逻辑回归分析表明,有 6 种 miRNA 与 MI 发生独立相关。其中,miR-223 和 miR-186 可靠地预测了 MI 患者的长期死亡率,尤其是在左心室射血分数(LVEF)调整后,miR-223(每增加一个单位的 HR 为 1.57, = 0.02)。Kaplan-Meier 生存分析提供了 miR-223 表达( = 0.028)的长期死亡率预测阈值。

结论-循环 miR-223 和 miR-186 是 MI 后长期死亡率的有前途的预测生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35c/9496068/12e40fc73ee9/biomolecules-12-01243-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35c/9496068/4a63e806b0b4/biomolecules-12-01243-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35c/9496068/12e40fc73ee9/biomolecules-12-01243-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35c/9496068/4a63e806b0b4/biomolecules-12-01243-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35c/9496068/12e40fc73ee9/biomolecules-12-01243-g002.jpg

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