A randomized, controlled comparison of different intensive lipid-lowering therapies in Chinese patients with non-ST-elevation acute coronary syndrome (NSTE-ACS): Ezetimibe and rosuvastatin versus high-dose rosuvastatin

被引:34
作者
Ran, Dan [1 ,2 ]
Nie, Hui-Juan [1 ]
Gao, Yu-Lin [1 ]
Deng, Song-Bai [1 ]
Du, Jian-Lin [1 ]
Liu, Ya-Jie [1 ]
Jing, Xiao-Dong [1 ]
She, Qiang [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 2, Dept Cardiol, 74 Linjiang Rd, Chongqing, Peoples R China
[2] Pengzhou Peoples Hosp, Dept Cardiol, Chengdu, Sichuan, Peoples R China
关键词
Ezetimibe; Rosuvastatin; Intensive lipid-lowering therapy; MYOCARDIAL-INFARCTION; HIGH-RISK; LDL CHOLESTEROL; PLUS EZETIMIBE; 10; MG; SIMVASTATIN; SAFETY; ATORVASTATIN; MANAGEMENT; REDUCTION;
D O I
10.1016/j.ijcard.2017.02.099
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Statin combined with ezetimibe demonstrates significant benefit in lowering low density lipid cholesterol (LDL-C) and cardiovascular events abroad, but whether intermediate intensity statins combined with ezetimibe is superior to high-intensity statin monotherapy in Chinese people is unknown. Methods: A total of 125 patients were randomly assigned to a intermediate intensity rosuvastatin group (rosuvastatin 10 mg/d, n = 42), high-dose rosuvastatin group (rosuvastatin 20 mg/d, n = 41) or combination therapy group (ezetimibe 10 mg/d and rosuvastatin 10 mg/d, n = 42) with a 12-week follow-up. The primary end point was the proportion of patients who achieved the 2011 ESC/EAS LDL-C goal <70 mg/dL (1.8 mmol/L) at week 12. Secondary end points included changes from baseline in lipids, the occurrence of all cardiovascular events, high-sensitivity C-reactive protein and safety markers. Results: The combination therapy group in the primary end point was significantly higher than rosuvastatin (20 mg) and rosuvastatin (10 mg) at week 12 (81.0% vs 68.3% vs 33.3%, P < 0.001). And the similar change was observed in reducing LDL-C levels at week 12 (67.28% vs 52.80% vs 43.89%, P < 0.001). The incidence of drug-related adverse events was much higher in the rosuvastatin 20 mg group than the rosuvastatin 10 mg group and the combination therapy group (17.0% vs 2.4% vs 4.8%, P < 0.05). Conclusions: The combination of rosuvastatin 10 mg/ezetimibe 10 mg was an effectively alternative therapy superior to rosuvastatin 20 mg or 10 mg with a greater effect on lowering LDL-C and a lower incidence of drug-related adverse events in Chinese patients. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 55
页数:7
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