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华法林治疗对活化凝血因子 VII 凝血活性的影响。

Influence of warfarin therapy on activated factor VII clotting activity.

作者信息

Lippi Giuseppe, Montagnana Martina, Salvagno Gian Luca, Poli Giovanni, Franchini Massimo, Guidi Gian Cesare

机构信息

Istituto di Chimica e Microscopia Clinica, Dipartimento di Scienze Morfologico-Biomediche, Università degli Studi di Verona, Verona, Italy.

出版信息

Blood Coagul Fibrinolysis. 2006 Apr;17(3):221-4. doi: 10.1097/01.mbc.0000220247.97164.ea.

DOI:10.1097/01.mbc.0000220247.97164.ea
PMID:16575262
Abstract

Oral anticoagulant therapy has been widely employed to prevent and treat a variety of thrombotic disorders, although a new generation of antithrombotic drugs, which offer inhibition of clot-bound as well as fluid-phase thrombin, has been developed and tested in several clinical trials. Although most anticoagulant responses to hydroxycoumarin compounds are well established, there are controversial evidences on their influence on activated factor VII (FVIIa). After analyzing the prothrombin time (PT) (International Normalized Ratio reference range, 0.92-1.08), factor VII clotting activity (FVII:C) (reference range, 75-130 U/dl) and activated factor VII clotting activity (FVIIa:C) (reference range, 30-110 U/l) in 46 consecutive patients on stable warfarin therapy for atrial fibrillation, a consistent trend towards decreased values of both FVII:C and FVIIa:C was observed as PT values increased. At moderate-intensity anticoagulation, with international normalized ratios between 2 and 3, the mean activities of FVII:C and FVIIa:C dropped to 28 U/dl (range, 9-61 U/dl) and 5.8 U/l (range, 1-18 U/l), respectively. Results of our investigations indicate that warfarin therapy decreases FVIIa:C, highlighting the potential benefits of oral anticoagulants in thrombotic disorders and other clinical conditions characterized by increased levels of FVIIa. Owing to the good correlation with FVIIa:C, we also hypothesize that the PT and/or FVII:C might be employed for monitoring recombinant FVIIa therapy.

摘要

口服抗凝治疗已被广泛用于预防和治疗各种血栓形成性疾病,尽管新一代抗血栓药物已被开发并在多项临床试验中进行了测试,这些药物能够抑制与凝块结合的凝血酶以及液相凝血酶。虽然大多数对羟基香豆素类化合物的抗凝反应已得到充分证实,但关于它们对活化因子VII(FVIIa)的影响仍存在有争议的证据。在分析了46例连续接受华法林稳定治疗心房颤动患者的凝血酶原时间(PT)(国际标准化比值参考范围为0.92 - 1.08)、因子VII凝血活性(FVII:C)(参考范围为75 - 130 U/dl)和活化因子VII凝血活性(FVIIa:C)(参考范围为30 - 110 U/l)后,观察到随着PT值升高,FVII:C和FVIIa:C值均呈持续下降趋势。在中等强度抗凝时,国际标准化比值在2至3之间,FVII:C和FVIIa:C的平均活性分别降至28 U/dl(范围为9 - 61 U/dl)和5.8 U/l(范围为1 - 18 U/l)。我们的研究结果表明,华法林治疗可降低FVIIa:C,突出了口服抗凝剂在血栓形成性疾病和其他以FVIIa水平升高为特征的临床状况中的潜在益处。由于与FVIIa:C具有良好的相关性,我们还推测PT和/或FVII:C可能用于监测重组FVIIa治疗。

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