Procoagulant effect of extracellular vesicles in patients after transcatheter aortic valve replacement or transcatheter aortic valve replacement with percutaneous coronary intervention

被引:0
作者
Hang Chi
Yibing Shao
Fangyu Xie
Jian Zhang
Guixin Zhang
Guihua Jiang
Dongxia Tong
Jihe Li
机构
[1] Qingdao University,Department of emergency, Qingdao Municipal Hospital, School of Medicine
[2] Qingdao Municipal Hospital,Department of Cardiology, School of Medicine
[3] Qingdao University,Department of General Practice
[4] People’s Hospital of Longhua,Department of General Surgery
[5] Qingdao FUWAI Cardiovascular Hospital,Department of Infectious Diseases
[6] People’s Hospital of Longhua,Department of Oncology, Qingdao Municipal Hospital, School of Medicine
[7] Qingdao University,undefined
来源
Journal of Thrombosis and Thrombolysis | 2023年 / 56卷
关键词
Severe aortic stenosis; Transcatheter aortic valve replacement; Percutaneous coronary intervention; Extracellular vesicles Procoagulant activity;
D O I
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学科分类号
摘要
Patients with severe aortic stenosis (AS) after replacement of the transcatheter aortic valve (TAVR) are more likely to develop thrombotic complications such as cerebral embolism and artificial valve thrombosis. However, the mechanism is not yet well defined. We aimed to explore the plasma extracellular vesicles (EVs) levels and their role in the induction of procoagulant activity (PCA) in patients receiving TAVR alone or TAVR with percutaneous coronary intervention (PCI). EVs were analyzed with flow cytometer. Markers of platelet and endothelial cell activation were quantified using selective enzyme-linked immunosorbent assay (ELISA) kits. Procoagulant activity (PCA) was assessed by clotting time, purified clotting complex assays, and fibrin production assays. Our results confirmed that EVs with positive phosphatedylserin (PS+EV), platelet EVs (PEVs) and positive tissue factor EVs (TF+EVs) were higher in patients following TAVR than before TAVR, particularly in TAVR with PCI. Furthermore, endothelial-derived EVs (EEVs) were also higher in patients after TAVR with PCI than pre-TAVR, however, the EEVs levels in TAVR alone patients were gradually reduce than pre-TAVR. In addition, we further proved that total EVs contributed to dramatically shortened coagulation time, increased intrinsic/extrinsic factor Xa and thrombin generation in patients after TAVR, especially in TAVR with PCI. The PCA was markedly attenuated by approximately 80% with lactucin. Our study reveals a previously unrecognized link between plasma EV levels and hypercoagulability in patients after TAVR, especially TAVR with PCI. Blockade of PS+EVs may improve the hypercoagulable state and prognosis of patients.
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页码:264 / 274
页数:10
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  • [1] Hu PP(2012)TAVR and SAVR: current treatment of aortic stenosis Clin Med Insights Cardiol 6 125-139
  • [2] Yutzey KE(2014)Calcific aortic valve disease: a consensus summary from the Alliance of investigators on calcific aortic valve disease Arterioscler Thromb Vasc Biol 34 2387-2393
  • [3] Demer LL(2016)Predictive factors of long-term survival in the octogenarian undergoing surgical aortic valve replacement: 12-year single-centre follow-up Heart Vessels 31 1798-1805
  • [4] Body SC(2014)Stroke after transcatheter aortic valve replacement: incidence, risk factors, prognosis, and preventive strategies Clin Cardiol 37 756-764
  • [5] Cappabianca G(2016)Predictors of early cerebrovascular events in patients with aortic stenosis undergoing transcatheter aortic valve replacement J Am Coll Cardiol 68 673-684
  • [6] Ferrarese S(2020)Aspirin with or without Clopidogrel after Transcatheter aortic-valve implantation N Engl J Med 383 1447-1457
  • [7] Musazzi A(2020)Anticoagulation with or without Clopidogrel after Transcatheter aortic-valve implantation N Engl J Med 382 1696-1707
  • [8] Mastoris I(2008)Membrane phosphatidylserine regulates surface charge and protein localization Science 319 210-213
  • [9] Schoos MM(2011)Microvesicles in hemostasis and thrombosis Circ Res 108 1284-1297
  • [10] Dangas GD(2007)Role of the extrinsic pathway of blood coagulation in hemostasis and thrombosis Arterioscler Thromb Vasc Biol 27 1687-1693