内科学
医学
类降脂药
冠状动脉疾病
心脏病学
载脂蛋白B
心肌梗塞
脂蛋白
剩余风险
胆固醇
不稳定型心绞痛
危险系数
冲程(发动机)
脂蛋白(a)
比例危险模型
心绞痛
置信区间
工程类
机械工程
作者
Takamitsu Nakamura,Jun–ei Obata,Mitsumasa Hirano,Yoshinobu Kitta,Daisuke Fujioka,Yukio Saitō,Ken‐ichi Kawabata,Kazuhiro Watanabe,Yosuke Watanabe,Hideto Mishina,Kiyotaka Kugiyama
标识
DOI:10.1016/j.atherosclerosis.2011.04.040
摘要
Objectives Triglycerides-rich lipoproteins are related to residual cardiovascular risk in patients on lipid-lowering treatment who achieve low-density lipoprotein cholesterol (LDL-C) goals. This study examined the predictive value of remnant lipoprotein levels for cardiovascular events in patients with coronary artery disease (CAD) with LDL-C levels <100 mg/dL on lipid-lowering therapy. Methods Serum levels of remnant lipoproteins (remnant-like lipoprotein particles cholesterol; RLP-C) were measured by an immunoseparation method in 560 patients with CAD who had LDL-C levels <100 mg/dL on lipid-lowering therapy, including statin (58%), fibrate (13%) or diet only (29%). All the patients were followed prospectively for a period of ≤36 months or until occurrence of one of the following events: cardiac death, non fatal myocardial infarction, unstable angina requiring coronary revascularization, or ischemic stroke. Results During a mean follow-up period of 33 months, 40 events occurred. Stepwise multivariate Cox proportional hazard analysis showed that RLP-C was a significant predictor of cardiovascular events after adjustment for known risk factors and lipid variables including triglycerides, non-high-density lipoprotein (HDL)-C, and total apolipoprotein B (HR 1.53, 95% CI 1.35–1.97, p < 0.01). The c-statistics showed that addition of RLP-C had a greater incremental effect on the predictive value of conventional risk factors than addition of non-HDL-C or total apolipoprotein B. Conclusions RLP-C was superior to non-HDL-C for predicting cardiovascular events in CAD patients with LDL-C levels <100 mg/dL on lipid-lowering treatment. Remnant lipoprotein may therefore be an important target for residual risk reduction after LDL-C goals on lipid lowering therapy.
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