Faber C G, Lodder J, Kessels F, Troost J
Department of Neurology, University Hospital Maastricht, Maastricht, The Netherlands.
Pathophysiol Haemost Thromb. 2003;33(1):52-8. doi: 10.1159/000071642.
The time course of the concentration of active thrombin in clotting plasma (the thrombogram) was measured by subsampling from platelet-rich plasma (PRP) and continuous chromogenic measurement of platelet-poor plasma (PPP) in 41 stroke patients under the age of 50, in whom stroke could not be attributed to cardioembolic disease, arterial dissection or vasculitis. A significant increase in the area under the thrombogram (endogenous thrombin potential, ETP) was seen in 23 patients. In 9 of them, ETP was increased in PRP but normal in PPP. High ETP in PRP was significantly associated with stroke, both in the middle and in the highest tercile of the ETP (odds ratio 5.1, range 1.8-15.1, and 3.7, range 1.3-10.3, respectively). A decreased sensitivity to the inhibitory action of thrombomodulin (TM) on thrombin generation was observed in 5 of 37 cases. No further definition of the cause of increased thrombin generation or TM resistance was attempted, except for the role of von Willebrand factor (vWF). ETP in PRP, platelet-derived procoagulant activity and vWF were correlated and higher in patients than in controls (p=0.002, p=0.045 and p=0.0006, respectively). This confirms the correlation between vWF level and stroke at young age found in epidemiological studies. It suggests that the role of vWF in thrombin generation, which has been demonstrated in vitro, may be the underlying mechanism of this correlation. In summary, hypercoagulability, defined as an increased capacity of the platelet plasma system to form thrombin, is found in over half of the patients under 50 years with an otherwise unexplained stroke. Sometimes it is due to increased plasma factor activity, sometimes to an increased procoagulant activity of the platelets.
通过从富含血小板血浆(PRP)中进行二次采样,并对41名年龄在50岁以下、卒中病因不能归因于心源性栓塞疾病、动脉夹层或血管炎的卒中患者的乏血小板血浆(PPP)进行连续发色测定,来测量凝血血浆中活性凝血酶浓度的时间进程(血栓图)。23名患者的血栓图曲线下面积(内源性凝血酶潜力,ETP)显著增加。其中9名患者,PRP中的ETP升高,但PPP中的ETP正常。PRP中高ETP与卒中显著相关,在ETP的中间和最高三分位数中均如此(优势比分别为5.1,范围1.8 - 15.1,以及3.7,范围1.3 - 10.3)。在37例中有5例观察到对血栓调节蛋白(TM)对凝血酶生成抑制作用的敏感性降低。除了血管性血友病因子(vWF)的作用外,未尝试对凝血酶生成增加或TM抵抗的原因进行进一步定义。PRP中的ETP、血小板衍生的促凝血活性和vWF相互关联,且患者中的这些指标高于对照组(分别为p = 0.002、p = 0.045和p = 0.0006)。这证实了流行病学研究中发现的vWF水平与年轻患者卒中之间的相关性。这表明在体外已得到证实的vWF在凝血酶生成中的作用可能是这种相关性的潜在机制。总之,在超过一半的50岁以下病因不明的卒中患者中发现了高凝状态,定义为血小板血浆系统形成凝血酶的能力增强。有时这是由于血浆因子活性增加,有时是由于血小板促凝血活性增加。