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血小板微小RNA表达可预测接受或未接受阿司匹林治疗的HeartMate3患者的出血情况。

Platelet microRNA Expression Can Predict Bleeding in HeartMate3 Patients Treated With or Without Aspirin.

作者信息

Foglieni Chiara, Ravanelli Davide, Lombardi Maria, Spartano Lucia, Pieri Marina, Ajello Silvia, Landoni Giovanni, Scandroglio Anna Mara, Consolo Filippo

机构信息

Atherosclerosis and Myocardial Disease Laboratory, Cardiovascular Research Center, IRCCS San Raffaele Scientific Institute, Via Olgettina 60, 20132, Milan, Italy.

Department of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

J Cardiovasc Transl Res. 2025 Jul 11. doi: 10.1007/s12265-025-10659-2.

DOI:10.1007/s12265-025-10659-2
PMID:40643853
Abstract

We tested whether platelet microRNAs (miRs) expression can predict bleeding in patients supported with the HeartMate3 (HM3) left ventricular assist device (LVAD). The levels of expression of platelet miR-126, miR-233, miR-151a, and miR-454 were prospectively measured in 12 consecutive patients pre-implant and during long-term follow-up and compared based on aspirin (ASA) or ASA-free therapy at discharge and bleeding events over the course of HM3 support. Median time of follow-up was 760 (574-844) days. Seven (58%) patients were discharged on ASA and 5 (42%) without ASA. Three (25%) patients experienced 10 bleeding episodes: one never received ASA, and two suffered from bleeding recurrency long after permanent ASA discontinuation. ASA had minimal influence on platelet miRs expression. The expression levels of platelet miR-454 were lower in bleeders vs. non-bleeders, both pre-implant and post-implant. This study suggests the existence of a patient-specific pro-hemorrhagic phenotype associated with a distinctive expression profile of platelet miR-454. Clinical Trial Registration: https://clinicaltrials.gov/ct2/show/NCT03255928 . ClinicalTrials.gov Identifier: NCT03255928.

摘要

我们测试了血小板微小RNA(miR)的表达是否能够预测接受HeartMate3(HM3)左心室辅助装置(LVAD)支持的患者的出血情况。前瞻性地测定了12例连续患者植入前及长期随访期间血小板miR-126、miR-233、miR-151a和miR-454的表达水平,并根据出院时是否接受阿司匹林(ASA)治疗或无ASA治疗以及在HM3支持过程中的出血事件进行比较。中位随访时间为760(574 - 844)天。7例(58%)患者出院时接受ASA治疗,5例(42%)未接受ASA治疗。3例(25%)患者发生了10次出血事件:1例从未接受过ASA治疗,2例在永久停用ASA后很长时间出现出血复发。ASA对血小板miR表达的影响极小。无论在植入前还是植入后,出血患者的血小板miR-454表达水平均低于未出血患者。本研究表明存在一种与血小板miR-454独特表达谱相关的患者特异性出血倾向表型。临床试验注册:https://clinicaltrials.gov/ct2/show/NCT03255928 。ClinicalTrials.gov标识符:NCT03255928。

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本文引用的文献

1
Understanding Platelet Activation in the Aeson Bioprosthetic Total Artificial Heart: Insights From Aspirin Treatment and Outcomes.了解埃宋生物人工全人工心脏中的血小板激活:阿司匹林治疗及结果的启示
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Intraplatelet miRNA-126 regulates thrombosis and its reduction contributes to platelet inhibition.血小板内 miRNA-126 调节血栓形成,其减少有助于血小板抑制。
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Aspirin and Hemocompatibility Events With a Left Ventricular Assist Device in Advanced Heart Failure: The ARIES-HM3 Randomized Clinical Trial.
阿司匹林与左心室辅助装置在晚期心力衰竭中的血液相容性事件:ARIES-HM3 随机临床试验。
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Blood. 2024 Feb 22;143(8):661-672. doi: 10.1182/blood.2022018096.
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Left ventricular assist devices promote changes in the expression levels of platelet microRNAs.左心室辅助装置促使血小板微小核糖核酸表达水平发生变化。
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The Potential Role of MiRs-139-5p and -454-3p in Endoglin-Knockdown-Induced Angiogenic Dysfunction in HUVECs.miRs-139-5p 和 -454-3p 在 endoglin 敲低诱导的 HUVECs 血管生成功能障碍中的潜在作用。
Int J Mol Sci. 2023 Mar 3;24(5):4916. doi: 10.3390/ijms24054916.
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Comprehensive Characterization of Platelet-Enriched MicroRNAs as Biomarkers of Platelet Activation.血小板富集 microRNAs 的全面特征分析作为血小板活化的生物标志物。
Cells. 2022 Apr 7;11(8):1254. doi: 10.3390/cells11081254.
8
Hyperadhesive von Willebrand Factor Promotes Extracellular Vesicle-Induced Angiogenesis: Implication for LVAD-Induced Bleeding.高黏附性血管性血友病因子促进细胞外囊泡诱导的血管生成:对左心室辅助装置诱导出血的影响
JACC Basic Transl Sci. 2022 Mar 28;7(3):247-261. doi: 10.1016/j.jacbts.2021.12.005. eCollection 2022 Mar.
9
2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.2022年美国心脏协会/美国心脏病学会/美国心力衰竭学会心力衰竭管理指南:美国心脏病学会/美国心脏协会临床实践指南联合委员会报告
Circulation. 2022 May 3;145(18):e895-e1032. doi: 10.1161/CIR.0000000000001063. Epub 2022 Apr 1.
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