医学
阀门更换
血小板
内科学
中性粒细胞胞外陷阱
纤维蛋白
狭窄
心脏病学
经皮冠状动脉介入治疗
内皮功能障碍
血小板活化
血小板缺乏血浆
内分泌学
凝血酶
炎症
免疫学
心肌梗塞
作者
Wu Wei,Dongxia Tong,Wei Xia,Bin Song,Guangwen Li,Lihui Zhou,Fangyu Xie,Chunquan Zhang,Y Liu,Haiyang Wang,Zhaona Du,Yibing Shao,Jihe Li
标识
DOI:10.1161/atvbaha.124.322376
摘要
BACKGROUND: Patients with severe aortic stenosis, undergoing transcatheter aortic valve replacement (TAVR), are more likely to develop thrombotic complications. However, the definite mechanisms underlying the hypercoagulation state remain unclear to date. Our objectives were to explore whether and how neutrophil extracellular traps (NETs) play a procoagulant role in patients after TAVR alone or TAVR with percutaneous coronary intervention within 1 year and further to evaluate their interactions with platelets and endothelial cells. METHODS: The levels of plasma NETs, platelets, and endothelial cell activation markers were analyzed by ELISA. NET formation was observed by immunofluorescence. Procoagulant activity was measured by clotting time, fibrin, and TAT (thrombin-antithrombin) complex generation assays. Phosphatidylserine exposure on cells was assessed by flow cytometry. RESULTS: Compared with pre-TAVR, controls, or severe aortic stenosis without TAVR patients, the plasma NET levels in patients after TAVR alone, especially TAVR with percutaneous coronary intervention, increased from 7 days, peaking at 3 months, and then gradually decreased until the 12th month. Furthermore, neutrophils and plasma from patients post-TAVR are more prone to promote NET formation; NETs from these patients markedly decreased clotting time and increased fibrin and TAT generation. Additionally, a high concentration of NETs induced platelet aggregation and exerted a strong cytotoxic effect on endothelial cells and transformed them into a procoagulant phenotype. CONCLUSIONS: These results lead us to believe that NETs contribute to the hypercoagulability in patients post-TAVR. Our study may provide a new target for preventing thrombotic complications in patients post-TAVR by blocking NET generation.
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