de Maat Moniek P M, Verschuur Maartje
Department of Hematology, Erasmus Medical Center, Rotterdam, The Netherlands.
Curr Opin Hematol. 2005 Sep;12(5):377-83. doi: 10.1097/01.moh.0000169287.51594.3b.
Many noninherited or inherited variations have been described in fibrinogen and they may affect the different functions of fibrinogen.
A number of the acquired variations in fibrinogen affect the properties of the fibrinogen molecule, such as the conversion rate to fibrin and/or the characteristics of the fibrin clot. Also, genetic polymorphisms are known that can affect the function of the fibrinogen molecule. In addition, some other genetic variants are associated with plasma levels of fibrinogen and with the increase of fibrinogen levels during an acute-phase reaction.
In this review the authors discuss the noninherited and inherited variations of fibrinogen and the clinical implications (e.g. when determining the risk of cardiovascular disease).
纤维蛋白原中已描述了许多非遗传性或遗传性变异,它们可能会影响纤维蛋白原的不同功能。
纤维蛋白原的一些获得性变异会影响纤维蛋白原分子的特性,例如转化为纤维蛋白的速率和/或纤维蛋白凝块的特性。此外,已知基因多态性会影响纤维蛋白原分子的功能。此外,一些其他基因变异与纤维蛋白原的血浆水平以及急性期反应期间纤维蛋白原水平的升高有关。
在本综述中,作者讨论了纤维蛋白原的非遗传性和遗传性变异及其临床意义(例如在确定心血管疾病风险时)。