Jenkins P Vince, O'Donnell James S
National Center for Hereditary Coagulation Disorders and Department of Haematology, Institute of Molecular Medicine, St. James's Hospital and Trinity College, Dublin, Ireland.
Transfusion. 2006 Oct;46(10):1836-44. doi: 10.1111/j.1537-2995.2006.00975.x.
For many years, an association between ABO histo-blood group and risk of thrombosis has been recognized. Blood group non-O (A, B, and AB) individuals have consistently been found to demonstrate increased incidence of both arterial and venous thrombotic disease, compared to group O individuals. This increased risk is attributable to the fact that ABO blood group influences plasma levels of a coagulation glycoprotein named von Willebrand factor (VWF). VWF levels are 25 percent higher in non-O compared to group O individuals. The mechanism by which ABO group determines plasma VWF levels has not been determined. ABO(H) carbohydrate antigenic determinants, however, are expressed on the N-linked glycan chains of circulating plasma VWF. This review will focus on the carbohydrate structures of VWF and recent studies suggesting that subtle variations in these structures (particularly differences in ABO blood group antigen expression) may have clinically significant effects on VWF proteolysis and clearance.
多年来,ABO组织血型与血栓形成风险之间的关联已得到认可。与O型血个体相比,非O型血(A、B和AB型)个体的动脉和静脉血栓性疾病发病率持续升高。这种风险增加归因于ABO血型会影响一种名为血管性血友病因子(VWF)的凝血糖蛋白的血浆水平。与O型血个体相比,非O型血个体的VWF水平高25%。ABO血型决定血浆VWF水平的机制尚未明确。然而,ABO(H)碳水化合物抗原决定簇在循环血浆VWF的N-连接聚糖链上表达。本综述将聚焦于VWF的碳水化合物结构以及近期研究,这些研究表明这些结构的细微变化(特别是ABO血型抗原表达的差异)可能对VWF的蛋白水解和清除产生临床显著影响。