Tikkanen M J, Helve E, Jäättelä A, Kaarsalo E, Lehtonen A, Malbecq W, Oksa H, Pääkkönen P, Salmi J, Veharanta T
Third Department of Medicine, University Central Hospital, Helsinki, Finland.
Am J Cardiol. 1988 Nov 11;62(15):35J-43J. doi: 10.1016/0002-9149(88)90005-7.
A randomized, double-blind 12-week comparison of lovastatin and gemfibrozil in the treatment of patients with primary hypercholesterolemia with normal or moderately elevated triglycerides was performed in 334 patients from 19 centers in Finland. Patients with "high" total serum cholesterol (240 to 300 mg/dl) constituted Stratum 1 and patients with "very high" total serum cholesterol (greater than 300 mg/dl) constituted Stratum 2. In Stratum 1, patients were randomly assigned to either lovastatin 20 mg nightly or gemfibrozil 600 mg twice daily, and in Stratum 2 to either lovastatin 40 mg nightly or gemfibrozil 600 mg twice daily. In both strata, the lovastatin dose was doubled after 6 weeks if serum cholesterol remained greater than 200 mg/dl. Ninety-two and 93% of the patients doubled their dose in Strata 1 and 2, respectively, resulting in average doses of 38.5 mg/day (Stratum 1) and 77.4 mg/day (Stratum 1) and 77.4 mg/day (Stratum 2) by week 12. The dose of gemifibrozil was kept constant. Lovastatin reduced low-density lipoprotein (LDL) cholesterol by 31 and 42% in Stratum 1 and 2, respectively. The corresponding reductions achieved by gemfibrozil were 13 and 18%. In both strata, as well as in patients with Type IIa and IIb hyperlipoproteinemia, lovastatin was approximately 2 to 4 times as effective as gemfibrozil in lowering LDL cholesterol. Although both drugs increased high-density lipoprotein (HDL) cholesterol concentrations, gemfibrozil was 1.5 to 3 times more effective. LDL/HDL cholesterol ratios decreased significantly more during lovastatin therapy. Both drugs reduced serum triglyceride levels, but gemfibrozil was much more effective.(ABSTRACT TRUNCATED AT 250 WORDS)
在芬兰19个中心的334名患者中,进行了一项随机、双盲、为期12周的研究,比较洛伐他汀和吉非贝齐治疗甘油三酯正常或轻度升高的原发性高胆固醇血症患者的疗效。血清总胆固醇“高”(240至300mg/dl)的患者构成第1组,血清总胆固醇“非常高”(大于300mg/dl)的患者构成第2组。在第1组中,患者被随机分配每晚服用20mg洛伐他汀或每日两次服用600mg吉非贝齐;在第2组中,患者被随机分配每晚服用40mg洛伐他汀或每日两次服用600mg吉非贝齐。在两组中,如果6周后血清胆固醇仍大于200mg/dl,洛伐他汀剂量在6周后加倍。第1组和第2组分别有92%和93%的患者剂量加倍,到第12周时,平均剂量分别为38.5mg/天(第1组)和77.4mg/天(第2组)。吉非贝齐的剂量保持不变。洛伐他汀在第1组和第2组中分别使低密度脂蛋白(LDL)胆固醇降低31%和42%。吉非贝齐相应的降低幅度为13%和18%。在两组以及IIa型和IIb型高脂蛋白血症患者中;洛伐他汀降低LDL胆固醇的效果约为吉非贝齐的2至4倍。虽然两种药物都提高了高密度脂蛋白(HDL)胆固醇浓度,但吉非贝齐的效果要高1.5至3倍。在洛伐他汀治疗期间,LDL/HDL胆固醇比值下降更为显著。两种药物都降低了血清甘油三酯水平,但吉非贝齐的效果要好得多。(摘要截选至250字)