Relation between carotid intima-media thickness, platelet surface activation and endothelial cell markers.

Haemostasis Pub Date : 1998-09-01 DOI:10.1159/000022442
N Ramsis, A A El-Hawary, E Ismail
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引用次数: 16

Abstract

Background: The role of platelet activation and endothelial cell damage in the pathogenesis of atherosclerosis was investigated.

Methods: Flow-cytometric detection of platelet activity was accomplished by measuring the surface expression of activated platelet glycoprotein IIb/IIIa (activated CD41) and the lysosomal integral membrane protein (CD63). Levels of thrombomodulin (TM) and von Willebrand factor (vWF) were estimated by the ELISA technique as markers of endothelial cell damage. These procedures were performed in healthy male subjects without obvious signs of atherosclerosis. Also, the intima-media thickness of the carotid artery was measured with high-resolution B- mode ultrasound to quantitate the presence and/or the extent of carotid atherosclerosis.

Results: According to ultrasound findings patients were divided into those with apparent evidence of atherosclerosis (AS+) with intima-media thickness >1.1 mm (n = 19) and those without such evidence (AS-) with intima-media thickness <1.1 mm (n = 17). The percentages of activated CD41 and CD63 surface antigen expression were significantly increased in the AS+ compared to AS- subjects. TM levels were elevated in the former group compared to the latter, while vWF levels were not different in the two groups. Multivariate analysis indicated the independent association of carotid atherosclerosis with each of the expression of activated CD41, CD63 as well as TM levels after adjustment of other risk factors.

Conclusion: This study demonstrates that platelets circulate in an enhanced activation state in asymptomatic atherosclerosis, which is closely related to the degree of endothelial cell damage as expressed by increased plasma levels of TM. The detection of platelet activation can be used as a potential marker for oncoming atherosclerosis.

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颈动脉内膜-中膜厚度、血小板表面活化与内皮细胞标志物的关系。
背景:研究血小板活化和内皮细胞损伤在动脉粥样硬化发病机制中的作用。方法:通过测定活化血小板糖蛋白IIb/IIIa(活化CD41)和溶酶体整体膜蛋白(CD63)的表面表达,完成血小板活性的流式细胞术检测。血栓调节素(TM)和血管性血友病因子(vWF)水平通过ELISA技术作为内皮细胞损伤的标志物进行测定。这些手术是在没有明显动脉粥样硬化迹象的健康男性受试者中进行的。同时,用高分辨率B型超声测量颈动脉内膜-中膜厚度,以量化颈动脉粥样硬化的存在和/或程度。结果:根据超声表现将患者分为内膜-中膜厚度>1.1 mm有明显动脉粥样硬化证据(AS+)组(n = 19)和内膜-中膜厚度无明显动脉粥样硬化证据(AS-)组(n = 19)。结论:本研究表明,无症状动脉粥样硬化患者血小板循环处于增强激活状态,这与血浆TM水平升高所表达的内皮细胞损伤程度密切相关。血小板活化的检测可作为动脉粥样硬化发生的潜在标志。
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