Serrano Feliciano A, El-Shahawy Mohamed, Solomon Richard J, Sobel Burton E, Schneider David J
Department of Medicine, University of Vermont, Burlington, Vermont, USA.
Thromb J. 2007 Jun 4;5:7. doi: 10.1186/1477-9560-5-7.
Increased platelet reactivity has been implicated in cardiovascular disease - the major cause of death in patients with end stage renal disease (ESRD). FcGammaRIIA is a component of glycoprotein VI and Ib-IX-V that mediate activation of platelets by collagen and von Willebrand factor. To determine whether expression of FcGammaRIIA impacts platelet reactivity we quantified its expression and platelet reactivity in 33 patients with ESRD who were undergoing hemodialysis.
Blood samples were obtained from patients immediately before hemodialysis and before administration of heparin. Platelet expression of FcGammaRIIA and the activation of platelets in response to low concentrations of convulxin (1 ng/ml, selected to mimic effects of collagen), thrombin (1 nM), adenosine diphosphate (ADP, 0.2 microM), or platelet activating factor (PAF, 1 nM) were determined with the use of flow cytometry in samples of whole blood anticoagulated with corn trypsin inhibitor (a specific inhibitor of Factor XIIa).
Patients were stratified with respect to the median expression of FcGammaRIIA. Patients with high platelet expression of FcGammaRIIA exhibited 3-fold greater platelet reactivity compared with that in those with low expression in response to convulxin (p < 0.01) and 2-fold greater activation in response to thrombin, ADP, and PAF (p < 0.05 for each). For each agonist, expression of FcGammaRIIA correlated modestly but positively with platelet reactivity. The strongest correlation was with thrombin-induced activation (r = 0.6, p < 0.001).
Increased platelet reactivity in response to low concentrations of diverse agonists is associated with high expression of FcGammaRIIA and may contribute to an increased risk of thrombosis in patients with ESRD.
血小板反应性增加与心血管疾病有关,而心血管疾病是终末期肾病(ESRD)患者的主要死因。FcγRIIA是糖蛋白VI和Ib-IX-V的组成部分,它们介导胶原蛋白和血管性血友病因子对血小板的激活。为了确定FcγRIIA的表达是否会影响血小板反应性,我们对33例正在接受血液透析的ESRD患者的FcγRIIA表达和血小板反应性进行了量化。
在血液透析前且未给予肝素之前,立即从患者采集血样。使用流式细胞术,在经玉米胰蛋白酶抑制剂(因子XIIa的特异性抑制剂)抗凝的全血样本中,测定FcγRIIA的血小板表达以及血小板对低浓度convulxin(1 ng/ml,选择该浓度以模拟胶原蛋白的作用)、凝血酶(1 nM)、二磷酸腺苷(ADP,0.2 μM)或血小板活化因子(PAF,1 nM)的反应性。
根据FcγRIIA的中位表达对患者进行分层。与低表达患者相比,FcγRIIA血小板高表达的患者对convulxin的反应性高3倍(p < 0.01),对凝血酶、ADP和PAF的反应性高2倍(每种情况p < 0.05)。对于每种激动剂,FcγRIIA的表达与血小板反应性呈适度但正相关。最强的相关性是与凝血酶诱导的激活相关(r = 0.6,p < 0.001)。
对低浓度多种激动剂的血小板反应性增加与FcγRIIA的高表达相关,可能会增加ESRD患者的血栓形成风险。