Brenner Benjamin, Kuperman Amir A, Watzka Matthias, Oldenburg Johannes
Thrombosis and Hemostasis Unit, Institute of Hematology, Rambam Medical Center, and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Semin Thromb Hemost. 2009 Jun;35(4):439-46. doi: 10.1055/s-0029-1225766. Epub 2009 Jul 13.
All vitamin K-dependent coagulation factors require normal function of gamma-glutamyl carboxylase and vitamin K epoxide reductase enzyme complex (VKORC1). Heritable dysfunction of gamma-glutamyl carboxylase or of the VKORC1 complex results in the secretion of poorly carboxylated vitamin K-dependent proteins that play a role in coagulation. The following review will summarize the clinical manifestations of vitamin K-dependent coagulation factors deficiency I and II and will provide a detailed explanation about the gene and protein structure, the function of the protein, and an analysis of the previously reported mutations. Laboratory assays used for diagnosis will be discussed, and treatment for various clinical settings will be recommended.
所有维生素K依赖性凝血因子都需要γ-谷氨酰羧化酶和维生素K环氧化物还原酶复合物(VKORC1)的正常功能。γ-谷氨酰羧化酶或VKORC1复合物的遗传性功能障碍会导致分泌出羧化不良的维生素K依赖性蛋白质,这些蛋白质在凝血过程中发挥作用。以下综述将总结维生素K依赖性凝血因子缺乏症I型和II型的临床表现,并将详细解释基因和蛋白质结构、蛋白质功能以及对先前报道的突变进行分析。还将讨论用于诊断的实验室检测方法,并推荐针对各种临床情况的治疗方法。