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首页> 外文期刊>European Journal of Haematology >Assessment of procoagulant potential in patients with reactive thrombocytosis and its association with platelet count
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Assessment of procoagulant potential in patients with reactive thrombocytosis and its association with platelet count

机译:评估活性血小板症患者的促血血管潜力及其与血小板计数的关系

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Abstract Objective We aimed to determine hemostatic changes and characterize the procoagulant potential among patients with reactive thrombocytosis ( RT ). Methods Sixty patients with RT (median platelet count 718?×?10 9 /L) and 20 healthy persons were tested for complete blood count, C‐reactive protein, von Willebrand factor ( VWF ), factor VIII and fibrinogen, and thrombin generation. Platelet studies, including light transmission aggregometry and Cone and Plate(let) Analyzer, were also conducted. Reticulated platelets and platelet P‐selectin expression were measured using flow cytometry. Results Compared to patients with mild thrombocytosis (platelet count 500‐700?×?10 9 /L; n?=?27), those with moderate‐to‐severe thrombocytosis (platelet count 700?×?10 9 /L; n?=?33) had significantly higher fibrinogen, factor VIII , and VWF antigen and activity levels; higher endogenous thrombin potential, peak thrombin generation and velocity index levels, and shorter time‐to‐peak thrombin level. VWF antigen and activity, fibrinogen, and factor VIII were positively associated with platelet count, whereas VWF activity/antigen ratio was inversely correlated. In a multivariate analysis of RT and control participants, only platelet count predicted endogenous thrombin potential with a positive‐linear correlation. No patients developed acquired von Willebrand syndrome. Conclusions As determined by thrombin generation, RT was associated with in vitro prothrombotic tendency, which correlated with platelet count. This may explain the increased thromboembolic risk previously reported in patients with RT .
机译:摘要目的我们旨在确定止血变化,并表征活性血小板减少症(RT)患者的促血管潜力。方法对RT(中位数血小板计数718〜×10 9 / L)和20种健康人进行六十六十患者进行完全血统计数,C反应蛋白,von Willebrand因子(VWF),因子VIII和纤维蛋白原,以及凝血酶产生。还进行了血小板研究,包括光传动聚集体和锥形和板(Let)分析仪。使用流式细胞术测量网状血小板和血小板p-选择蛋白表达。结果与轻度血小板减少症的患者相比(血小板计数500-700?×10 9 / L; n?= 27),那些具有中度至严重的血小盲症(血小板计数& 700?×10 9 / L; n?= 33)具有显着更高的纤维蛋白原,因子VIII和VWF抗原和活性水平;更高的内源性凝血酶电位,峰凝血酶产生和速度指数水平,较短的峰值凝血酶水平。 VWF抗原和活性,纤维蛋白原和因子VIII与血小板计数呈正相关,而VWF活性/抗原比对同时相关。在RT和对照参与者的多变量分析中,只有血小板计数预测具有正线性相关性的内源性凝血酶电位。没有患者开发过von Willebrand综合征。通过凝血酶产生确定的结论,RT与体外普形细胞趋势相关,与血小板计数相关。这可以解释RT的患者之前报道的增加的血栓栓塞风险增加。

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