Bots A F E, Kastelein J J P
Zuiderhoed General Practice, 's-Hertogenbosch, Amsterdam, the Netherlands.
Int J Clin Pract. 2005 Dec;59(12):1387-94. doi: 10.1111/j.1368-5031.2005.00708.x.
DISCOVERY Netherlands was an open-label, randomised, multicentre study (D3560/L00003) designed to compare the effects of rosuvastatin with those of atorvastatin, simvastatin or pravastatin on low-density lipoprotein cholesterol (LDL-C) goal achievement in a primary care setting. Patients (n = 1,215) with type IIa or type IIb hypercholesterolaemia and cardiovascular risk of >20% or a history of coronary heart or other atherosclerotic vascular disease were randomised to receive treatment with rosuvastatin 10 mg (n = 621), atorvastatin 10 mg (n = 189), simvastatin 20 mg (n = 194) or pravastatin 40 mg (n = 211) for 12 weeks. Significantly, more patients achieved 1998 and 2003 European LDL-C goals with rosuvastatin than with other statins after 12 weeks (p < 0.001). Rosuvastatin reduced LDL-C and total cholesterol levels significantly more than other statins, both in patients who were statin-naïve and in patients who had received previous statin treatment (p < 0.05). All treatments were similarly well tolerated. In conclusion, greater reductions in LDL-C were achieved with rosuvastatin compared with atorvastatin, simvastatin and pravastatin, enabling more patients to achieve European LDL-C goals.
荷兰探索研究是一项开放标签、随机、多中心研究(D3560/L00003),旨在比较在初级保健环境中,瑞舒伐他汀与阿托伐他汀、辛伐他汀或普伐他汀对实现低密度脂蛋白胆固醇(LDL-C)目标的影响。患有IIa型或IIb型高胆固醇血症且心血管风险>20%或有冠心病或其他动脉粥样硬化性血管疾病病史的患者(n = 1215)被随机分配接受10 mg瑞舒伐他汀(n = 621)、10 mg阿托伐他汀(n = 189)、20 mg辛伐他汀(n = 194)或40 mg普伐他汀(n = 211)治疗12周。值得注意的是,12周后,与其他他汀类药物相比,使用瑞舒伐他汀实现2003年欧洲LDL-C目标的患者显著更多(p < 0.001)。在未接受过他汀类药物治疗的患者和之前接受过他汀类药物治疗的患者中,瑞舒伐他汀降低LDL-C和总胆固醇水平的幅度均显著大于其他他汀类药物(p < 0.05)。所有治疗的耐受性相似。总之,与阿托伐他汀、辛伐他汀和普伐他汀相比,瑞舒伐他汀降低LDL-C的幅度更大,使更多患者能够实现欧洲LDL-C目标。