Effects of Combination of Ezetimibe and Rosuvastatin on Coronary Artery Plaque in Patients with Coronary Heart Disease

被引:39
|
作者
Wang, Xiaofang [1 ]
Zhao, Xiaoyan [1 ]
Li, Ling [1 ]
Yao, Haimu [1 ]
Jiang, Yan [2 ]
Zhang, Jinying [1 ]
机构
[1] Zhengzhou Univ, Coll Med, Affiliated Hosp 1, Dept Cardiol, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Coll Med, Affiliated Hosp 5, Dept Neurol, Zhengzhou 450052, Peoples R China
来源
HEART LUNG AND CIRCULATION | 2016年 / 25卷 / 05期
关键词
Ezetimibe; Rosuvastatin; Coronary artery plaque; High-sensitivity C-reactive protein; Interleukin-6; Matrix metalloproteinase-9; INTESTINAL CHOLESTEROL ABSORPTION; ATHEROSCLEROSIS; HYPERCHOLESTEROLEMIA; SIMVASTATIN; TRIAL;
D O I
10.1016/j.hlc.2015.10.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In approximately 80% of cardiovascular disease-related deaths, patients suffer from coronary atherosclerotic heart disease. Ezetimibe is the first intestinal cholesterol absorption inhibitor. Its combination with statins for treating coronary atherosclerotic heart disease has attracted attention worldwide. Methods The study group comprised 106 patients with coronary atherosclerotic heart disease and hyperlipidaemia. Each was randomly assigned to one of two groups: (1) Ezetimibe (10 mg, once a night) plus rosuvastatin (10 mg, once a night) (n = 55) or (2) Rosuvastatin alone (10 mg, once a night) (n = 51). The primary endpoint was new or recurrent myocardial infarction, unstable angina pectoris, cardiac death, and stroke. Blood lipid, high-sensitivity C-reactive protein (hsCRP), interleukin-6 (IL-6), and matrix metalloproteinase-9 (MMP-9) levels were measured before treatment and at one, six and 12 months after treatment. Coronary plaque size and compositional changes were determined using intravascular ultrasonography. Results The combination of ezetimibe plus rosuvastatin decreased total cholesterol, low-density lipoprotein cholesterol, hsCRP, IL-6, and MMP-9 levels at six and 12 months after treatment. Statistical significance was detected between two groups. At 12 months, the plaque burden, plaque cross-sectional area, and percentage of necrotic plaque composition were significantly lower in the combination group than in rosuvastatin alone group (P < 0.05). And compared with rosuvastatin alone group, the primary endpoint decreased more effectively in combination group. Conclusions The combination of ezetimibe and rosuvastatin apparently diminishes lipid levels and plaque burden and improves plaque stability, which may be associated with the potent inhibitory effects of ezetimibe and rosuvastatin on inflammatory cytokines.
引用
收藏
页码:459 / 465
页数:7
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