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Comparison of the efficacy of rosuvastatin versus atorvastatin in reducing apolipoprotein B/apolipoprotein A-1 ratio in patients with acute coronary syndrome: Results of the CENTAURUS study

机译:瑞舒伐他汀与阿托伐他汀在降低急性冠脉综合征患者载脂蛋白B /载脂蛋白A-1比率中的功效比较:CENTAURUS研究结果

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摘要

Background. The mechanism underlying statin-induced event reduction in patients with acute coronary syndrome remains unclear. Aims. To assess the efficacy of rosuvastatin 20 mg versus atorvastatin 80 mg in reducing the apolipoprotein B/apolipoprotein A-1 (apoB/apoA-1) ratio at 3 months. Non-inferiority of rosuvastatin 20 mg versus atorvastatin 80 mg in reducing low-density lipoprotein cholesterol at 1 and 3 months was also assessed. Methods. Patients with non-ST-elevation acute coronary syndrome were enrolled into this randomized, double blind, parallel-group trial. Results. In total, 753 patients (369, rosuvastatin 20 mg; 384, atorvastatin 80 mg) were included in the intention-to-treat analysis; 478 patients (226, rosuvastatin 20 mg; 252, atorvastatin 80 mg) were included in the per-protocol analysis. Rosuvastatin 20 mg was more effective than atorvastatin 80 mg in decreasing apoB/apoA-1 ratio at 1 month (-44.4% vs -42.9%, p = 0.02) but not at 3 months (both -44.4%, p = 0.87). Low-density lipoprotein cholesterol decreased by similar to 50% after 1 and 3 months in both groups. Non-inferiority of rosuvastatin 20 mg versus atorvastatin 80 mg was demonstrated at 1 month (difference, -0.3% [95% confidence interval, -2.7; +2.1]), but not at 3 months (+1.0% [-1.6; 3.5]) (intention-to-treat analysis). In the per-protocol analysis, non-inferiority of rosuvastatin 20 mg was demonstrated at both 1 (-0.7% [-3.5; 2.0]) and 3 (-0.5% [-3.5; 2.5]) months. Conclusion. In patients with non-ST-elevation acute coronary syndrome, rosuvastatin 20 mg decreased apoB/apoA-1 ratio at 1 month more than atorvastatin 80 mg. No difference could be shown at 3 months; thus, the primary endpoint was not met. (C) 2010 Published by Elsevier Masson SAS.
机译:背景。他汀类药物引起的急性冠状动脉综合征患者事件减少的机制尚不清楚。目的为了评估瑞舒伐他汀20 mg与阿托伐他汀80 mg在降低3个月时载脂蛋白B /载脂蛋白A-1(apoB / apoA-1)比率方面的功效。还评估了瑞舒伐他汀20 mg与阿托伐他汀80 mg在1个月和3个月时降低低密度脂蛋白胆固醇的非劣效性。方法。非ST段抬高的急性冠状动脉综合征患者参加了这项随机,双盲,平行组试验。结果。意图治疗分析总共包括753例患者(369例瑞舒伐他汀20毫克; 384例阿托伐他汀80毫克);方案分析中包括478例患者(226,瑞舒伐他汀20 mg; 252,阿托伐他汀80 mg)。瑞舒伐他汀20 mg比阿托伐他汀80 mg在降低apoB / apoA-1比率在1个月时(-44.4%对-42.9%,p = 0.02)更有效,但在3个月时却无效果(两者-44.4%,p = 0.87)。两组在1个月和3个月后,低密度脂蛋白胆固醇降低了约50%。罗苏伐他汀20 mg与阿托伐他汀80 mg的非劣效性在1个月时得到证实(差异为-0.3%[95%置信区间,-2.7; +2.1]),但在3个月时没有表现出非劣效性(+ 1.0%[-1.6; 3.5] ])(意向性分析)。在按方案分析中,罗苏伐他汀20 mg在1(-0.7%[-3.5; 2.0])和3(-0.5%[-3.5; 2.5])个月均显示出非劣效性。结论。在非ST段抬高的急性冠状动脉综合征患者中,罗舒伐他汀20 mg在1个月时比阿托伐他汀80 mg降低了apoB / apoA-1比。三个月后无差异;因此,未达到主要终点。 (C)2010由Elsevier Masson SAS发布。

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