Weisweiler P
iphar Institut für Klinische Pharmakologie GmbH, Munich, Fed. Rep. of Germany.
Arzneimittelforschung. 1988 Jul;38(7):925-7.
29 patients with primary hypercholesterolemia were treated for 8 weeks each with either bezafibrate (200 mg t.i.d.) or gemfibrozil (600 mg b.i.d.) in a randomized cross-over trial. Compared to placebo bezafibrate was significantly more effective on low density lipoprotein (LDL)-cholesterol (-28% versus -18%) and the LDL/high density lipoprotein (HDL) ratio (-34% versus -24%) by exploratory statistics. There was also a trend for a more marked reduction of bezafibrate on total cholesterol and apoliproprotein B as well as more pronounced increase in HDL-cholesterol and apolipoprotein A-I. The triglyceride reduction tended to be more extensive with gemfibrozil. Complicance to both drugs was good. No side-effects were observed. The results are considered important with respect to the potential of bezafibrate in reducing the risk of cardiovascular disease.
在一项随机交叉试验中,29例原发性高胆固醇血症患者分别接受苯扎贝特(200毫克,每日三次)或吉非贝齐(600毫克,每日两次)治疗,各为期8周。通过探索性统计分析,与安慰剂相比,苯扎贝特在降低低密度脂蛋白(LDL)胆固醇方面(-28%对-18%)以及LDL/高密度脂蛋白(HDL)比值方面(-34%对-24%)显著更有效。苯扎贝特在降低总胆固醇和载脂蛋白B方面也有更明显降低的趋势,同时在升高HDL胆固醇和载脂蛋白A-I方面更为显著。吉非贝齐在降低甘油三酯方面的作用似乎更广泛。两种药物的依从性都很好。未观察到副作用。就苯扎贝特在降低心血管疾病风险方面的潜力而言,这些结果被认为是重要的。