Wu San-Chiang, Shiang Jeng-Chuan, Lin Shoa-Lin, Wu Te-Lang, Huang Wei-Chun, Chiou Kuan-Rau, Liu Chun-Peng
Department of Human Resource Management, National Sun Yat-Sen University, Kaohsiung, Taiwan.
Heart Vessels. 2005 Sep;20(5):217-23. doi: 10.1007/s00380-005-0836-6.
Information of the effect of statin on lipoproteins such as apolipoprotein (apo) A-I, lipoprotein (a) [Lp (a)], or apolipoprotein B levels is limited. This investigation was a crossover study designed to evaluate the efficacy and safety of atorvastatin and simvastatin in patients with hyperlipidemia. Sixty-six patients were involved in the study. Group I consisted of 32 patients, who were first treated with atorvastatin (10 mg) then switched to simvastatin (10 mg). Group II consisted of 34 patients, who were first treated with simvastatin then switched to atorvastatin. Each regimen was used for 3 months (phase I), stopped for 2 months, and then restarted for another 3 months (phase II). Both statins effectively reduced total cholesterol, low-density lipoprotein cholesterol (LDL-C), apo B, and Lp (a) (P < 0.001 in all comparisons). A significant increase in the high-density lipoprotein cholesterol (HDL-C) was noted after both statin treatments (P < 0.05 in all comparisons). Both statins caused an increase in the apo A-I levels, and the extent of changes in apo A-I revealed no difference between the two drugs. Compared to the simvastatin group, there were more patients in the atorvastatin group achieving the National Cholesterol Education Program ATP-III LDL-C goal (P < 0.05) and European LDL-C goal (P < 0.001). Both treatments were well tolerated; no patient was withdrawn from the study. This study demonstrates that both statins can effectively improve lipid profiles in patients with hyperlipidemia. Atorvastatin is more effective in helping patients reach the ATP-III and European LDL-C goals than simvastatin at the same dosage.
他汀类药物对载脂蛋白(apo)A-I、脂蛋白(a)[Lp(a)]等脂蛋白或载脂蛋白B水平影响的相关信息有限。本研究是一项交叉研究,旨在评估阿托伐他汀和辛伐他汀在高脂血症患者中的疗效和安全性。66例患者参与了该研究。第一组由32例患者组成,他们先接受阿托伐他汀(10毫克)治疗,然后换用辛伐他汀(10毫克)。第二组由34例患者组成,他们先接受辛伐他汀治疗,然后换用阿托伐他汀。每种治疗方案使用3个月(第一阶段),停药2个月,然后再重新开始使用3个月(第二阶段)。两种他汀类药物均能有效降低总胆固醇、低密度脂蛋白胆固醇(LDL-C)、载脂蛋白B和Lp(a)(所有比较中P<0.001)。两种他汀类药物治疗后均观察到高密度脂蛋白胆固醇(HDL-C)显著升高(所有比较中P<0.05)。两种他汀类药物均使载脂蛋白A-I水平升高,且两种药物载脂蛋白A-I的变化程度无差异。与辛伐他汀组相比,阿托伐他汀组更多患者达到了美国国家胆固醇教育计划成人治疗组第三次报告(ATP-III)的LDL-C目标(P<0.05)和欧洲LDL-C目标(P<0.001)。两种治疗耐受性均良好;无患者退出研究。本研究表明,两种他汀类药物均可有效改善高脂血症患者的血脂谱。在相同剂量下,阿托伐他汀在帮助患者达到ATP-III和欧洲LDL-C目标方面比辛伐他汀更有效。