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微小 RNA 作为心血管疾病患者血小板功能和成熟的生物标志物。

MicroRNA as Biomarkers for Platelet Function and Maturity in Patients with Cardiovascular Disease.

机构信息

Department of Clinical Biochemistry, Thrombosis and Haemostasis Research Unit, Aarhus University Hospital, Aarhus, Denmark.

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Thromb Haemost. 2022 Feb;122(2):181-195. doi: 10.1055/s-0041-1730375. Epub 2021 Jun 6.

Abstract

Patients with cardiovascular disease (CVD) are at increased risk of suffering myocardial infarction. Platelets are key players in thrombus formation and, therefore, antiplatelet therapy is crucial in the treatment and prevention of CVD. MicroRNAs (miRs) may hold the potential as biomarkers for platelet function and maturity. This systematic review was conducted using the guidelines of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). To identify studies investigating the association between miRs and platelet function and maturity in patients with CVD, PubMed and Embase were searched on October 13 and December 13, 2020 without time boundaries. Risk of bias was evaluated using a standardized quality assessment tool. Of the 16 included studies, 6 studies were rated "good" and 10 studies were rated "fair." In total, 45 miRs correlated significantly with platelet function or maturity (rho ranging from -0.68 to 0.38, all  < 0.05) or differed significantly between patients with high platelet reactivity and patients with low platelet reactivity (-values ranging from 0.0001 to 0.05). Only four miRs were investigated in more than two studies, namely miR-223, miR-126, miR-21 and miR-150. Only one study reported on the association between miRs and platelet maturity. In conclusion, a total of 45 miRs were associated with platelet function or maturity in patients with CVD, with miR-223 and miR-126 being the most frequently investigated. However, the majority of the miRs were only investigated in one study. More data are needed on the potential use of miRs as biomarkers for platelet function and maturity in CVD patients.

摘要

患有心血管疾病 (CVD) 的患者发生心肌梗死的风险增加。血小板是血栓形成的关键因素,因此,抗血小板治疗对于 CVD 的治疗和预防至关重要。微小 RNA (miRs) 可能作为血小板功能和成熟的生物标志物具有潜力。本系统评价按照系统评价和荟萃分析的首选报告项目 (PRISMA) 指南进行。为了确定研究 miR 与 CVD 患者血小板功能和成熟之间的相关性,于 2020 年 10 月 13 日和 12 月 13 日在 PubMed 和 Embase 上进行了无时间限制的搜索。使用标准化质量评估工具评估偏倚风险。在纳入的 16 项研究中,有 6 项研究被评为“良好”,10 项研究被评为“一般”。共有 45 个 miR 与血小板功能或成熟显著相关(rho 范围为-0.68 至 0.38,均<0.05),或在高血小板反应性患者与低血小板反应性患者之间存在显著差异(-值范围为 0.0001 至 0.05)。只有四个 miR 在两项以上的研究中被研究过,即 miR-223、miR-126、miR-21 和 miR-150。只有一项研究报道了 miR 与血小板成熟之间的关系。总之,共有 45 个 miR 与 CVD 患者的血小板功能或成熟相关,miR-223 和 miR-126 是研究最多的。然而,大多数 miR 只在一项研究中被研究过。需要更多的数据来研究 miR 作为 CVD 患者血小板功能和成熟的生物标志物的潜在用途。

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