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Changes in Circulating Extracellular Vesicles in Patients with ST-Elevation Myocardial Infarction and Potential Effects of Remote Ischemic Conditioning—A Randomized Controlled Trial

机译:ST升高心肌梗死患者循环细胞外囊泡的变化及远程缺血调理 - 一种随机对照试验的潜在影响

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摘要

(1) Background: Extracellular vesicles (EVs) have been recognized as a cellular communication tool with cardioprotective properties; however, it is unknown whether cardioprotection by remote ischemic conditioning (RIC) involves EVs. (2) Methods: We randomized patients with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) to additionally receive a protocol of RIC or a sham-intervention. Blood was taken before and immediately, 24 h, four days and one month after PCI. Additionally, we investigated EVs from healthy volunteers undergoing RIC. EVs were characterized by a high-sensitive flow cytometer (Beckman Coulter Cytoflex S, Krefeld, Germany). (3) Results: We analyzed 32 patients (16 RIC, 16 control) and five healthy volunteers. We investigated platelet-, endothelial-, leukocyte-, monocyte- and granulocyte-derived EVs and their pro-thrombotic sub-populations expressing superficial phosphatidylserine (PS ). We did not observe a significant effect of RIC on the numbers of circulating EVs, although granulocyte-derived EVs were significantly higher in the RIC group. In line, RIC had not impact on EVs in healthy volunteers. Additionally, we observed changes of PS /PEV, EEVs and PS /CD15 EVs irrespective of RIC with time following STEMI. 4) Conclusion: We provide further insights into the course of different circulating EVs during the acute and sub-acute phases of STEMI. With respect to the investigated EV populations, RIC seems to have no effect, with only minor differences found for granulocyte EVs.
机译:(1)背景:细胞外囊泡(EVS)已被识别为具有心脏保护性能的细胞通信工具;然而,尚不清楚远程缺血调理(RIC)是否涉及EVS。 (2)方法:我们随机化了患有ST升高心肌梗死(STEMI)的患者进行一次经皮冠状动脉干预(PCI),另外接受RIC的协议或假干预。在PCI后24小时,24小时,4天和一个月服用血液。此外,我们研究了正在进行RIC的健康志愿者的EV。 EVS的特征在于一种高敏感的流动凝纹仪(Beckman Coulter Cytoflex S,Krefeld,德国)。 (3)结果:我们分析了32名患者(16次,16名控制)和五名健康志愿者。我们研究了表达浅表磷脂酰丝氨酸(PS)的血小板,内皮,白细胞,单核细胞和粒细胞衍生的EV及其促血栓形成亚群。尽管RIC组在粒细胞衍生的EV显着高,但我们并没有观察到Ric对循环EV的数量的显着影响。在线,Ric对健康志愿者的EVS没有影响。此外,我们观察到PS / PEV,EEV和PS / CD15 EV的变化,而无论HTEMI遵循时间。 4)结论:我们在STEMI的急性和亚急性阶段期间提供了进一步的循环EVS过程中的进一步见解。关于调查的EV群体,RIC似乎没有效果,只发现粒细胞EVS的微小差异。

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