Scanu Angelo M, Bamba Ravi
Department of Medicine, University of Chicago, Chicago, Illinois 60637, USA.
Am J Cardiol. 2008 Apr 17;101(8A):44B-47B. doi: 10.1016/j.amjcard.2008.02.031.
Over the years, niacin has gained recognition as an atheroprotective agent, in part because of its capacity to lower the plasma levels of cholesterol, triglycerides, and very-low- and low-density lipoproteins and to substantially raise high-density lipoprotein. In high doses, niacin has also been reported to lower the plasma level of lipoprotein(a) (Lp[a]). However, the published research on the subject suffers from a lack of uniformity regarding patient selection, drug dose, length of administration, and methods for plasma Lp(a) quantification. In this report, the authors examine the most relevant niacin-related Lp(a) studies and hypothetical mechanisms of drug action, also considering the emerging notion of Lp(a) as a potential proinflammatory entity.
多年来,烟酸已被公认为一种抗动脉粥样硬化药物,部分原因在于其能够降低血浆中胆固醇、甘油三酯以及极低密度脂蛋白和低密度脂蛋白的水平,并能显著提高高密度脂蛋白水平。高剂量的烟酸也被报道可降低血浆脂蛋白(a)[Lp(a)]水平。然而,关于该主题已发表的研究在患者选择、药物剂量、给药时长以及血浆Lp(a)定量方法方面缺乏一致性。在本报告中,作者审视了与烟酸相关的最具相关性的Lp(a)研究以及药物作用的假设机制,同时也考虑了Lp(a)作为一种潜在促炎实体这一新兴概念。