Nijiati Muyesai, Saidaming Abulijiang, Tuohuti Adelijiang, Guoqing Li, Rong Du
Clin Lab. 2016 Sep 1;62(9):1619-1624. doi: 10.7754/Clin.Lab.2016.150534.
A limited number of reports are analyzing the etiology and the mechanism of coronary heart disease by examining the source cells of micro particles (MPs) in coronary heart disease patients with percutaneous coronary intervention (PCI). This study aims to explore the circulating platelet micro particles (PMPs) content variation in the blood stream and the mechanism of MPs-inducing thrombosis in patients operated with coronary stenting, with the intent to analyze the impact of PMPs on thrombosis and in-stent restenosis.
3000 patients with coronary heart disease were successfully operated with PCI. Subsequently, 100 patients and 50 healthy subjects were selected and divided into three groups: 1) normal control group (group A, 50 cases) of healthy subjects; 2) stenting + thrombosis group (group B, 50 cases); 3) stenting + non-thrombosis group (group C, 50 cases). Venous blood was drawn from the three groups of subjects to prepare platelet-free plasma, which was subjected to flow cytometry to examine the content of PMPs. In the meantime, the blood samples from the three groups of subjects were induced with 1 x 105 MPs from the patients in the stenting + thrombosis group, and the changes of thrombin-antithrombin (TAT) were observed.
PMPs' red fluorescence from group C was significantly more intense than that in the PMPs from group A, and the difference was statistically significant (p < 0.05). No significant difference was observed when comparing the content of PMPs in group B with the content in group A (p > 0.05). Thrombin in group B was increased significantly compared with thrombin content in group C, and the difference was statistically significant (p < 0.05). The thrombin level difference between group B and group C was not statistically significant (p > 0.05).
The content of PMPs in the patients with thrombosis after stenting was significantly increased, and the PMPs may induce the generation of thrombin. The PMPs' content variation in the peripheral blood circulation may be used to predict in-stent thrombosis and to evaluate therapeutic efficacy in the clinic.
目前仅有少数报告通过检测经皮冠状动脉介入治疗(PCI)的冠心病患者微粒(MPs)的来源细胞,来分析冠心病的病因和机制。本研究旨在探讨冠状动脉支架置入术患者血流中循环血小板微粒(PMPs)含量的变化以及MPs诱导血栓形成的机制,以分析PMPs对血栓形成和支架内再狭窄的影响。
3000例冠心病患者成功接受PCI手术。随后,选取100例患者和50例健康受试者,分为三组:1)健康受试者正常对照组(A组,50例);2)支架置入+血栓形成组(B组,50例);3)支架置入+无血栓形成组(C组,50例)。采集三组受试者静脉血制备无血小板血浆,采用流式细胞术检测PMPs含量。同时,用支架置入+血栓形成组患者的1×105个MPs诱导三组受试者的血样,观察凝血酶-抗凝血酶(TAT)的变化。
C组PMPs的红色荧光强度明显高于A组PMPs,差异有统计学意义(p<0.05)。B组与A组PMPs含量比较,差异无统计学意义(p>0.05)。B组凝血酶含量较C组显著升高,差异有统计学意义(p<0.05)。B组与C组凝血酶水平差异无统计学意义(p>0.05)。
支架置入术后血栓形成患者的PMPs含量显著升高,PMPs可能诱导凝血酶的产生。外周血液循环中PMPs含量的变化可用于预测支架内血栓形成并评估临床治疗效果。