Department of Biochemistry, University of Vermont, Colchester, VT, USA.
Thromb Res. 2010 Oct;126(4):262-9. doi: 10.1016/j.thromres.2010.07.002. Epub 2010 Aug 14.
More than 80% of cerebrovascular events are ischemic and largely thromboembolic by nature. We evaluated whether plasma factor composition and thrombin generation dynamics might be a contributor to the thrombotic phenotype of ischemic cerebrovascular events.
We studied (1) 100 patients with acute ischemic stroke (n=50) or transient ischemic attack (TIA) (n=50) within the first 24 hours from symptom onset, and (2) 100 individuals 1 to 4 years following ischemic stroke (n=50) or TIA (n=50). The tissue factor pathway to thrombin generation was simulated with a mathematical model using plasma levels of clotting factors (F)II, V, VII, VIII, IX, X, antithrombin and free tissue factor pathway inhibitor (TFPI).
The plasma levels of free TFPI, FII, FVIII, and FX were higher, while antithrombin was lower, in the acute patients compared to the previous event group (all p≤0.02). Thrombin generation during acute events was enhanced, with an 11% faster maximum rate, a 15% higher maximum level and a 26% larger total production (all p<0.01). The increased thrombin generation in acute patients was determined by higher FII and lower antithrombin, while increased free TFPI mediated this effect. When the groups are classified by etiology, all stroke sub-types except cardioembolic have increased TFPI and decreased AT and total thrombin produced.
Augmented thrombin generation in acute stroke/TIA is to some extent determined by altered plasma levels of coagulation factors.
超过 80%的脑血管事件为缺血性,且本质上大多为血栓栓塞性。我们评估了血浆因子组成和凝血酶生成动力学是否可能是缺血性脑血管事件血栓表型的一个促成因素。
我们研究了(1)发病后 24 小时内的 100 例急性缺血性脑卒中(n=50)或短暂性脑缺血发作(TIA)(n=50)患者,以及(2)缺血性脑卒中(n=50)或 TIA(n=50)后 1 至 4 年的 100 例个体。使用数学模型模拟组织因子途径向凝血酶生成,该模型使用血浆中凝血因子(F)II、V、VII、VIII、IX、X、抗凝血酶和游离组织因子途径抑制剂(TFPI)的水平。
与前一次事件组相比,急性患者的血浆游离 TFPI、FII、FVIII 和 FX 水平更高,而抗凝血酶水平更低(均 p≤0.02)。急性事件期间的凝血酶生成增强,最大速率快 11%,最大水平高 15%,总生成量高 26%(均 p<0.01)。急性患者的凝血酶生成增加是由 FII 升高和抗凝血酶降低引起的,而游离 TFPI 的增加介导了这种作用。当按病因对组进行分类时,除心源性栓塞外的所有脑卒中亚型均增加了 TFPI,降低了 AT 和总凝血酶的产生。
急性脑卒中/TIA 中凝血酶生成的增加在一定程度上是由凝血因子血浆水平的改变决定的。