Bradford R H, Shear C L, Chremos A N, Dujovne C, Downton M, Franklin F A, Gould A L, Hesney M, Higgins J, Hurley D P
Lipid Research Clinic, Oklahoma Medical Research Foundation, Oklahoma City 73104.
Arch Intern Med. 1991 Jan;151(1):43-9. doi: 10.1001/archinte.151.1.43.
In the Expanded Clinical Evaluation of Lovastatin (EXCEL) Study, a multicenter, double-blind, diet- and placebo-controlled trial, we evaluated the efficacy and safety of lovastatin in 8245 patients with moderate hypercholesterolemia. Patients were randomly assigned to receive placebo or lovastatin at a dosage of 20 mg once daily, 40 mg once daily, 20 mg twice daily, or 40 mg twice daily for 48 weeks. Lovastatin produced sustained, dose-related (P less than .001) changes as follows (for dosages of 20 to 80 mg/d): decreased low-density lipoprotein-cholesterol level (24% to 40%), increased high-density lipoprotein-cholesterol level (6.6% to 9.5%), decreased total cholesterol level (17% to 29%), and decreased triglyceride level (10% to 19%). The National Cholesterol Education Program's low-density lipoprotein-cholesterol level goal of less than 4.14 mmol/L (160 mg/dL) was achieved by 80% to 96% of patients, while the less than 3.36 mmol/L (130 mg/dL) goal was achieved by 38% to 83% of patients. The difference between lovastatin and placebo in the incidence of clinical adverse experiences requiring discontinuation was small, ranging from 1.2% at 20 mg twice daily to 1.9% at 80 mg/d. Successive transaminase level elevations greater than three times the upper limit of normal were observed in 0.1% of patients receiving placebo and 20 mg/d of lovastatin, increasing to 0.9% in those receiving 40 mg/d and 1.5% in those receiving 80 mg/d of lovastatin (P less than .001 for trend). Myopathy, defined as muscle symptoms with a creatine kinase elevation greater than 10 times the upper limit of normal, was found in only one patient (0.1%) receiving 40 mg once daily and four patients (0.2%) receiving 80 mg/d of lovastatin. Thus, lovastatin, when added after an adequate trial of a prudent diet, is a highly effective and generally well-tolerated treatment for patients with moderate hypercholesterolemia.
在洛伐他汀扩展临床评估(EXCEL)研究中,这是一项多中心、双盲、饮食及安慰剂对照试验,我们评估了洛伐他汀对8245例中度高胆固醇血症患者的疗效和安全性。患者被随机分配接受安慰剂或洛伐他汀,剂量分别为每日一次20毫克、每日一次40毫克、每日两次20毫克或每日两次40毫克,为期48周。洛伐他汀产生了持续的、与剂量相关的(P小于0.001)变化如下(对于20至80毫克/天的剂量):低密度脂蛋白胆固醇水平降低(24%至40%),高密度脂蛋白胆固醇水平升高(6.6%至9.5%),总胆固醇水平降低(17%至29%),甘油三酯水平降低(10%至19%)。80%至96%的患者实现了国家胆固醇教育计划设定的低密度脂蛋白胆固醇水平目标,即低于4.14毫摩尔/升(160毫克/分升),而38%至83%的患者实现了低于3.36毫摩尔/升(130毫克/分升)的目标。因临床不良事件需要停药的发生率,洛伐他汀与安慰剂之间的差异很小,从每日两次20毫克时的1.2%到80毫克/天时的1.9%不等。在接受安慰剂和每日20毫克洛伐他汀的患者中,0.1%观察到连续转氨酶水平升高超过正常上限的三倍,在接受40毫克/天的患者中升至0.9%,在接受80毫克/天洛伐他汀的患者中升至1.5%(趋势P小于0.001)。肌病定义为肌肉症状伴肌酸激酶升高超过正常上限的10倍,仅在一名接受每日一次40毫克的患者(0.1%)和四名接受80毫克/天洛伐他汀的患者(0.2%)中发现。因此,在经过适当的谨慎饮食试验后加用洛伐他汀,对中度高胆固醇血症患者是一种高效且普遍耐受性良好的治疗方法。