Pró-Sangue Foundation, University of São Paulo Medical School, São Paulo, Brazil.
Thromb Res. 2010 Jan;125(1):38-43. doi: 10.1016/j.thromres.2009.04.018. Epub 2009 May 17.
Pulmonary arterial hypertension (PAH) is frequently associated with thrombotic events, particularly involving the pulmonary microcirculation at sites of vascular injury. We therefore decided to analyse protease-activated receptor 1 (PAR1), a key element in the activation of human platelets by thrombin, in PAH patients in stable clinical condition.
Using flow cytometry, we analyzed platelet PAR1 density, PAR1-mediated exposure of P-selectin and the formation of platelet-leukocyte aggregates in 30 PAH patients aged 11 to 78 years (median 50.5 years). The control group consisted of 25 healthy subjects with the same age range as patients.
In patients, total platelet PAR1 density and uncleaved PAR1 density correlated negatively with platelet count (r(2)=0.33 and r(2)=0.34 respectively, p<0.0015). In patients with a low platelet count (<150x10(9) platelets/L), both densities were increased relative to controls (82% and 33% respectively, p<0.05). Thrombin peptide-induced platelet exposure of P-selectin was directly related to total and uncleaved PAR1 density (respectively, r(2)=0.33 and r(2)=0.29, p<0.0025) and increased in subjects with low platelet count (46% versus those with normal platelet count, p<0.05). Patients with low platelet count had decreased in vitro thrombin-induced formation of platelet-leukocyte aggregates (57% decrease versus controls, p<0.05).
There seems to be a subpopulation of PAH patients with increased propensity to thrombotic events as suggested by increased platelet PAR1 expression and PAR-mediated surface exposure of P-selectin associated with decreased platelet count.
肺动脉高压(PAH)常伴有血栓形成事件,特别是在血管损伤部位的肺微循环中。因此,我们决定分析蛋白酶激活受体 1(PAR1),它是凝血酶激活人血小板的关键因素,在处于稳定临床状态的 PAH 患者中进行分析。
我们使用流式细胞术分析了 30 名年龄在 11 至 78 岁(中位数 50.5 岁)的 PAH 患者和 25 名年龄相同的健康对照者的血小板 PAR1 密度、PAR1 介导的 P-选择素暴露和血小板-白细胞聚集体的形成。
在患者中,总血小板 PAR1 密度和未切割 PAR1 密度与血小板计数呈负相关(r(2)=0.33 和 r(2)=0.34,p<0.0015)。在血小板计数低(<150x10(9) 血小板/L)的患者中,两种密度均高于对照组(分别为 82%和 33%,p<0.05)。凝血酶肽诱导的血小板 P-选择素暴露与总 PAR1 和未切割 PAR1 密度直接相关(分别为 r(2)=0.33 和 r(2)=0.29,p<0.0025),在血小板计数低的患者中增加(与血小板计数正常的患者相比,增加 46%,p<0.05)。血小板计数低的患者体外凝血酶诱导的血小板-白细胞聚集体形成减少(与对照组相比减少 57%,p<0.05)。
似乎有一部分 PAH 患者具有增加的血栓形成倾向,这表明血小板 PAR1 表达增加和 PAR 介导的 P-选择素表面暴露与血小板计数减少有关。