Seed M, Doherty E, Stubbs P
Department of Medicine, Charing Cross Hospital, London, UK.
J Cardiovasc Risk. 1995 Jun;2(3):206-15.
New data on the interactions between lipoprotein (a) [Lp(a)] and the coagulation-fibrinolytic system, which emphasize the importance of the activity of lysine-binding sites on apolipoprotein (a) [apo(a)], provide an increasingly strong basis for the role of Lp(a) in thrombosis. Further insights into the genetic control of Lp(a) levels show that inherited factors other than the size of the apo(a) gene are important. The clinical relationship between Lp(a) and coronary heart disease has been more firmly established by two further large prospective cohort studies. The consensus that the concentration of Lp(a) does not predict the outcome of thrombolytic therapy still holds, although Lp(a) does affect endogenous fibrinolysis after myocardial infarction. The effect of Lp(a) on mortality should soon be known.
关于脂蛋白(a)[Lp(a)]与凝血-纤溶系统相互作用的新数据强调了载脂蛋白(a)[apo(a)]上赖氨酸结合位点活性的重要性,为Lp(a)在血栓形成中的作用提供了越来越有力的依据。对Lp(a)水平遗传控制的进一步深入研究表明,apo(a)基因大小以外的遗传因素也很重要。另外两项大型前瞻性队列研究更有力地证实了Lp(a)与冠心病之间的临床关系。尽管Lp(a)确实会影响心肌梗死后的内源性纤溶,但Lp(a)浓度不能预测溶栓治疗结果这一共识仍然成立。Lp(a)对死亡率的影响很快就会揭晓。