Illingworth DR, Stein EA, Knopp RH, Hunninghake DB, Davidson MH, Dujovne CA, Miller VT, Tobert JA, Laskarzewski PM, Isaacsohn JL, Bacon SP, Tate AC
Department of Medicine, Medical Research Laboratories, Portland, Oregon, USA
J Cardiovasc Pharmacol Ther. 1996 Jan;1(1):23-30. doi: 10.1177/107424849600100105.
Inhibitors of hydroxymethylglutaryl co-enzyme A reductase are widely used for the treatment of hypercholesterolemia. Physicians and third-party payers need an accurate measure of their relative potency and hypolipidemic efficacy. We have therefore compared simvastatin against fluvastatin, the newest member of this class. METHODS AND RESULTS: One hundred fifty-eight hypercholesterolemic patients in seven United States lipid clinics participated in this balanced double-blind incomplete block study. After a placebo-diet run-in period, patients received treatment with active drug for three consecutive 5-week periods, with measurement of lipids in a NHLBI-CDC standardized central laboratory at the end of each period. Each patient was randomly assigned to three of the following five treatments: simvastatin 5 mg, 10 mg, and 20 mg and fluvastatin 20 mg and 40 mg. The mean percent reductions in low density lipoprotein cholesterol from baseline were 21, 27, 32, 16, and 23 respectively. The simvastatin/fluvastatin milligram potency ratio was 6.8 (95% CI, 5.3-9.3). At the same 20 mg dose, simvastatin produced an effect on LDL cholesterol approximately double that of fluvastatin and resulted in 46% of patients achieving their National Cholesterol Education Program low density lipoprotein cholesterol target levels, compared to 12% for fluvastatin. CONCLUSIONS: Fluvastatin at its maximal dose of 40 mg daily is approximately equivalent to simvastatin 5 mg daily. Higher doses of simvastatin are considerably more effective in the treatment of primary hypercholesterolemia.
羟甲基戊二酰辅酶A还原酶抑制剂被广泛用于治疗高胆固醇血症。医生和第三方支付方需要准确衡量它们的相对效力和降血脂疗效。因此,我们将辛伐他汀与该类药物的最新成员氟伐他汀进行了比较。
美国七家血脂诊所的158名高胆固醇血症患者参与了这项平衡双盲不完全区组研究。在经过安慰剂饮食导入期后,患者连续三个为期5周的时间段接受活性药物治疗,每个时间段结束时在国立卫生研究院心肺血液研究所-疾病控制与预防中心标准化中央实验室测量血脂。每位患者被随机分配接受以下五种治疗中的三种:辛伐他汀5毫克、10毫克和20毫克,以及氟伐他汀20毫克和40毫克。低密度脂蛋白胆固醇相对于基线的平均降低百分比分别为21%、27%、32%、16%和23%。辛伐他汀/氟伐他汀毫克效力比为6.8(95%可信区间,5.3 - 9.3)。在相同的20毫克剂量下,辛伐他汀对低密度脂蛋白胆固醇产生的效果约为氟伐他汀的两倍,并且46%的患者达到了美国国家胆固醇教育计划的低密度脂蛋白胆固醇目标水平,而氟伐他汀为12%。
氟伐他汀每日最大剂量40毫克大约相当于辛伐他汀每日5毫克。更高剂量的辛伐他汀在治疗原发性高胆固醇血症方面效果显著更佳。