Division of Atherosclerosis and Lipoprotein Disorders, Presbyterian Cardiovascular Institute, 125 Baldwin Avenue, Suite 200, Charlotte, NC 28204, USA.
Curr Cardiol Rep. 2009 Nov;11(6):468-75. doi: 10.1007/s11886-009-0067-z.
Managing low-density lipoprotein (LDL) is an integral part of clinical practice. What remains controversial is whether we are using the best measure of LDL quantity for this purpose. Historically, the cholesterol content of LDL particles (LDLC) has been used to express LDL quantity. However, because of variability in the cholesterol carried in LDL particles, frequent disagreement occurs between LDLC and particle measures of LDL quantity, including apolipoprotein B-100 (apo B) or nuclear magnetic resonance (NMR) LDL particle number (LDL-P). Studies consistently demonstrate apo B and LDL-P are superior predictors of coronary heart disease (CHD) risk and superior indicators of low CHD risk on lipid-lowering therapy. Recent recommendations advocate that, in addition to LDLC and non-high-density lipoprotein cholesterol, apo B (or NMR LDL-P) be used as a target of therapy. This article reviews the rationale supporting these recommendations and provides a model for integrating LDL particle measures in clinical practice.
管理低密度脂蛋白 (LDL) 是临床实践的重要组成部分。目前仍存在争议的是,我们是否正在使用最佳的 LDL 数量指标来实现这一目标。从历史上看,LDL 颗粒中的胆固醇含量(LDLC)一直被用于表示 LDL 数量。然而,由于 LDL 颗粒中胆固醇的变异性,LDLC 与 LDL 数量的颗粒指标(包括载脂蛋白 B-100 [apo B] 或磁共振 [NMR] LDL 颗粒数 [LDL-P])之间经常存在分歧。研究一致表明,apo B 和 LDL-P 是冠心病 (CHD) 风险的更好预测指标,也是降脂治疗中低 CHD 风险的更好指标。最近的建议主张,除了 LDLC 和非高密度脂蛋白胆固醇外,apo B(或 NMR LDL-P)也应作为治疗的靶点。本文回顾了支持这些建议的基本原理,并提供了一种将 LDL 颗粒指标整合到临床实践中的模型。