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在普伐他汀限制冠状动脉粥样硬化(PLAC-I)试验中脂蛋白亚类水平和低密度脂蛋白大小与冠状动脉疾病进展的关系。

Relations of lipoprotein subclass levels and low-density lipoprotein size to progression of coronary artery disease in the Pravastatin Limitation of Atherosclerosis in the Coronary Arteries (PLAC-I) trial.

作者信息

Rosenson Robert S, Otvos James D, Freedman David S

机构信息

Preventive Cardiology Center, Division of Cardiology, Department of Medicine, Northwestern University Medical School, Chicago, Illinois, USA.

出版信息

Am J Cardiol. 2002 Jul 15;90(2):89-94. doi: 10.1016/s0002-9149(02)02427-x.

Abstract

Lipoprotein subclass measurements may enhance the prediction of coronary artery disease (CAD) risk, but clinical application of such information has been hindered by the relatively laborious and time-consuming nature of laboratory measurement methods. In this study, lipoprotein subclass analyses were performed on frozen plasma samples from 241 participants in the Pravastatin Limitation of Atherosclerosis in the Coronary arteries Trial using an automated nuclear magnetic resonance technique. The objective was to determine if levels of these subclasses provided additional information on the progression of CAD, based on the change in the minimum lumen diameter, over a 3-year period. After adjustment for race, sex, age, treatment group, baseline lumen diameter, and chemically measured levels of triglycerides, low-density lipoprotein (LDL) cholesterol, and high-density lipoprotein (HDL) cholesterol, on-trial predictors (p <0.05) of progression included an elevated LDL particle number, and levels of small LDL and small HDL. Within treatment groups, CAD progression was most strongly related to the LDL particle number (placebo) and levels of small HDL (pravastatin). In logistic regression models that adjusted for chemically determined lipid levels and other covariates, a small LDL level > or = 30 mg/dl (median) was associated with a ninefold increased risk of CAD progression (p <0.01) in the placebo group. These results indicate that levels of various lipoprotein subclasses may provide useful information on CAD risk even if levels of traditional risk factors are known.

摘要

脂蛋白亚类检测可能会增强对冠状动脉疾病(CAD)风险的预测,但此类信息的临床应用一直受到实验室检测方法相对繁琐且耗时的特性的阻碍。在本研究中,使用自动核磁共振技术对冠状动脉普伐他汀限制动脉粥样硬化试验中241名参与者的冷冻血浆样本进行了脂蛋白亚类分析。目的是根据最小管腔直径在3年期间的变化,确定这些亚类的水平是否能提供有关CAD进展的额外信息。在对种族、性别、年龄、治疗组、基线管腔直径以及化学测定的甘油三酯、低密度脂蛋白(LDL)胆固醇和高密度脂蛋白(HDL)胆固醇水平进行调整后,试验期间CAD进展的预测指标(p<0.05)包括LDL颗粒数量增加以及小LDL和小HDL水平升高。在各治疗组中,CAD进展与LDL颗粒数量(安慰剂组)和小HDL水平(普伐他汀组)最为密切相关。在对化学测定的血脂水平和其他协变量进行调整的逻辑回归模型中,安慰剂组中小LDL水平≥30mg/dl(中位数)与CAD进展风险增加9倍相关(p<0.01)。这些结果表明,即使已知传统风险因素的水平,各种脂蛋白亚类的水平也可能提供有关CAD风险的有用信息。

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