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组织因子途径抑制剂是血友病患者凝血酶生成的主要决定因素。

Tissue factor pathway inhibitor is the main determinant of thrombin generation in haemophilic patients.

机构信息

CIS-EMSE, SAINBIOSE, Ecole Nationale Supérieure des Mines de Saint-Etienne, Saint Etienne, France.

INSERM, U1059, SAINBIOSE, Université de Lyon, UJM-Saint-Etienne, Saint-Etienne, France.

出版信息

Haemophilia. 2019 Mar;25(2):343-348. doi: 10.1111/hae.13679. Epub 2019 Jan 28.

Abstract

The thrombin generation (TG) assay evaluates haemostatic balance, which is influenced by the levels of many coagulation factors and inhibitors. Our objective was to identify the determinant factors of TG in haemophilia A (HA) and haemophilia B (HB) patients and to compare them to those in healthy controls. Coagulation factor and inhibitor levels, and TG, were measured in platelet-poor plasma from 40 patients with HA, 32 patients with HB and 40 healthy subjects. Data were analysed using multiple regression models. In HA patients, factor VIII was a positive determinant of endogenous thrombin potential (ETP) and peak, whereas tissue factor pathway inhibitor (TFPI) and factor V were negative determinants of ETP and peak. In HB patients, FIX was a positive determinant of ETP and peak, FVII being a positive determinant of peak. Antithrombin and protein S (PS) were negative determinants of ETP while FX was a negative determinant of peak. Above all, in HB patients, TFPI was a negative determinant of ETP and peak. In healthy subjects, FVIII was a positive determinant of ETP and peak, whereas FX and protein S were negative determinants of these parameters. TFPI was not a negative determinant of either peak or ETP. In haemophilic patients, the determinant factors of TG are all implicated in FXa generation and inhibition, the crucial determinant factor being TFPI whatever the type of haemophilia, A or B. These findings contribute to the rationale that recently place TFPI as a target for innovative therapies of haemophilia.

摘要

凝血酶生成 (TG) 测定评估止血平衡,其受到许多凝血因子和抑制剂水平的影响。我们的目的是确定血友病 A (HA) 和血友病 B (HB) 患者 TG 的决定因素,并将其与健康对照组进行比较。我们在血小板缺乏的血浆中测量了 40 名 HA 患者、32 名 HB 患者和 40 名健康受试者的凝血因子和抑制剂水平以及 TG。使用多元回归模型分析数据。在 HA 患者中,VIII 因子是内源性凝血酶潜能 (ETP) 和峰值的正决定因素,而组织因子途径抑制剂 (TFPI) 和因子 V 是 ETP 和峰值的负决定因素。在 HB 患者中,FIX 是 ETP 和峰值的正决定因素,FVII 是峰值的正决定因素。抗凝血酶和蛋白 S (PS) 是 ETP 的负决定因素,而 FX 是峰值的负决定因素。最重要的是,在 HB 患者中,TFPI 是 ETP 和峰值的负决定因素。在健康受试者中,VIII 因子是 ETP 和峰值的正决定因素,而 FX 和蛋白 S 是这些参数的负决定因素。TFPI 既不是峰值也不是 ETP 的负决定因素。在血友病患者中,TG 的决定因素都与 FXa 的产生和抑制有关,无论血友病的类型是 A 型还是 B 型,TFPI 都是关键的决定因素。这些发现有助于最近将 TFPI 作为血友病创新治疗的靶点的原理。

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