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Comparison of the efficacy and tolerability of simvastatin and atorvastatin in the treatment of hypercholesterolemia

机译:辛伐他汀和阿托伐他汀治疗高胆固醇血症的疗效和耐受性比较

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摘要

Background: Simvastatin and atorvastatin are effective statins for treating hypercholesterolemia. Hypothesis: The study was undertaken to compare the efficacy and tolerability of simvastatin 20 and 40 mg/day and atorvastatin 10 and 20 mg/day. Methods: In this multinational, open‐label, crossover study, 258 patients with primary hypercholesterolemia were randomized after 4 weeks of diet plus placebo to once‐daily administration of a starting dose sequence of simvastatin (20 mg) or atorvastatin (10 mg), or a higher dose sequence of simvastatin (40 mg) or atorvastatin (20 mg) for 6 weeks. Patients were then switched after a 1‐week washout to the corresponding starting or higher dose of the alternate drug for a second 6‐week period. The primary endpoint was the mean percent change from baseline to Week 6 in low‐density lipoprotein (LDL) cholesterol; percent changes from baseline in total cholesterol, high‐density lipoprotein cholesterol, triglycerides, and apolipoprotein B were also compared. Safety was assessed through adverse experiences and laboratory measurements. Results: Both statins produced statistically significant improvements in all measured plasma lipids and lipoproteins. The main treatment comparison showed no statistically significant difference in changes in LDL cholesterol and triglycerides, whereby the overall effects were comparable when doses of 20 mg and 40 mg of simvastatin were compared with atorvastatin 10 mg and 20 mg. The mean percent reductions for LDL cholesterol from baseline to Week 6 ranged from 35–42% for the entire study cohort. An LDL cholesterol level ≤ 130 mg/dl (3.4 mmol/l) was achieved in approximately 70% of patients treated with both drugs in this study. Simvastatin and atorvastatin were well tolerated at the doses studied. Conclusion: In patients with hypercholesterolemia, the most commonly used doses of simvastatin and atorvastatin produced similar changes in LDL cholesterol and achieved an LDL cholesterol level ≤ 130 mg/dl (3.4 mmol/l) in a similar number of patients. Both statins were well tolerated.
机译:背景:辛伐他汀和阿托伐他汀是治疗高胆固醇血症的有效他汀类药物。假设:进行这项研究以比较辛伐他汀20和40 mg /天和阿托伐他汀10和20 mg /天的疗效和耐受性。方法:在这项跨国,开放标签,交叉研究中,将258名原发性高胆固醇血症患者在饮食4周后加安慰剂后随机分配给辛伐他汀(20 mg)或阿托伐他汀(10 mg)的起始剂量,每日一次,或较高剂量的辛伐他汀(40 mg)或阿托伐他汀(20 mg)服用6周。然后,在1周的冲洗后,患者在第二个6周期间转为使用相应的起始剂量或更高剂量的替代药物。主要终点是低密度脂蛋白(LDL)胆固醇从基线到第6周的平均百分比变化;还比较了总胆固醇,高密度脂蛋白胆固醇,甘油三酸酯和载脂蛋白B与基线相比的百分比变化。通过不良经验和实验室测量评估安全性。结果:两种他汀类药物在所有测得的血浆脂质和脂蛋白上均产生统计学上的显着改善。主要治疗比较显示LDL胆固醇和甘油三酸酯的变化无统计学差异,因此当将20 mg和40 mg辛伐他汀与10 mg和20 mg阿托伐他汀进行比较时,总体效果相当。在整个研究队列中,从基线到第6周LDL胆固醇的平均减少百分比为35-42%。在这项研究中,使用这两种药物治疗的患者中约有70%的LDL胆固醇水平达到≤130 mg / dl(3.4 mmol / l)。辛伐他汀和阿托伐他汀在所研究的剂量下耐受性良好。结论:在高胆固醇血症患者中,最常用的辛伐他汀和阿托伐他汀剂量在LDL胆固醇中产生相似的变化,并且在相似数量的患者中,LDL胆固醇水平≤130 mg / dl(3.4 mmol / l)。两种他汀类药物均耐受良好。

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