首页> 外文期刊>Journal of vascular surgery >Aspirin resistance among long-term aspirin users after carotid endarterectomy and controls: flow cytometric measurement of aspirin-induced platelet inhibition.
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Aspirin resistance among long-term aspirin users after carotid endarterectomy and controls: flow cytometric measurement of aspirin-induced platelet inhibition.

机译:颈动脉内膜切除术后长期服用阿司匹林的人和对照组中的阿司匹林耐药性:流式细胞仪检测阿司匹林诱导的血小板抑制作用。

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BACKGROUND: Numerous studies have indicated that some patient subpopulations do not respond to the antithrombotic effects of aspirin. The objective of this study was to evaluate aspirin-induced inhibition of platelet cyclooxygenase (COX) using a flow cytometric technique in long-term aspirin users after carotid endarterectomy (CEA) and controls with newly diagnosed carotid stenosis not taking aspirin and to compare these results with platelet function analyzer measurements. METHODS: The study included 86 patients with a history of CEA on long-term aspirin therapy (100 mg daily) and 29 age-matched patients with newly diagnosed carotid artery stenosis not taking aspirin. Platelet-rich plasma diluted with phosphate-buffered saline was incubated with arachidonic acid (ARA) at a final concentration of 80 micromol/L. After staining with phycoerythrin-labeled anti-P-selectin (CD62p) antibody, platelet CD62p-antigen expression was measured on a flow cytometer. RESULTS: Flow cytometric measurement of ARA-induced platelet activation showed an inhibition of ARA-induced platelet stimulation in all patients on aspirin therapy, whereas all but two controls (95%) showed expected platelet reactivity. In contrast, results of the platelet function analyzer measurements were normal in 16% of aspirin-treated patients. CONCLUSIONS: Flow cytometric measurement of CD62p expression on platelets after incubation with ARA proved to be a practicable tool to monitor aspirin-induced inhibition of platelet COX. Results in patients on long-term low-dose aspirin therapy show that the inability of aspirin to inhibit platelet COX for both symptomatic and asymptomatic patients with high-grade internal carotid artery stenosis is a very rare event. So-called aspirin resistance detected quite frequently by platelet function analyzer measurement is most likely from COX-independent mechanisms.
机译:背景:大量研究表明,某些患者亚群对阿司匹林的抗血栓形成作用无反应。这项研究的目的是使用流式细胞术评估长期使用阿司匹林的患者在颈动脉内膜切除术(CEA)和新诊断的颈动脉狭窄未服用阿司匹林的对照组中使用阿司匹林诱导的血小板环氧化酶(COX)抑制作用,并比较这些结果用血小板功能分析仪测量。方法:该研究包括86例长期服用阿司匹林的CEA病史(每天100 mg)和29例年龄相匹配的新诊断为未使用阿司匹林的颈动脉狭窄患者。用磷酸盐缓冲盐水稀释的富血小板血浆与花生四烯酸(ARA)一起孵育,终浓度为80 micromol / L。用藻红蛋白标记的抗P选择素(CD62p)抗体染色后,在流式细胞仪上测量血小板CD62p抗原的表达。结果:流式细胞仪检测ARA诱导的血小板活化显示在所有接受阿司匹林治疗的患者中均抑制了ARA诱导的血小板刺激,而除两个对照组(95%)外,所有患者均显示出预期的血小板反应性。相反,在阿司匹林治疗的患者中,血小板功能分析仪的测量结果是正常的,为16%。结论:流式细胞术检测血小板与ARA孵育后CD62p表达是监测阿司匹林诱导的对血小板COX抑制的实用工具。长期接受小剂量阿司匹林治疗的患者的结果表明,对于患有严重颈内动脉狭窄的有症状和无症状患者,阿司匹林无法抑制血小板COX是非常罕见的事件。血小板功能分析仪测量经常检测到的所谓阿司匹林耐药性很可能是由COX独立机制引起的。

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