Oster P, Schlierf G, Lang P D, Mordasini R, Vollmar J
Pharmatherapeutica. 1985;4(5):267-77.
Diurnal lipid and lipoprotein profiles were measured in 28 healthy volunteers after 10-day treatment periods with placebo, bezafibrate (200 mg 3-times daily) or clofibrate (500 mg 3-times daily) in a double-blind, parallel trial. The two drugs lowered fasting triglyceride and cholesterol levels (p less than or equal to 0.05 for cholesterol with bezafibrate vs placebo). Diurnal triglyceride profiles were lowest with bezafibrate due to lowest fasting triglycerides. Alimentary lipaemia with placebo was mild and due to increased VLDL-triglycerides, while the other lipoprotein lipids and total plasma cholesterol remained virtually unchanged during the day. Bezafibrate (half-life 2 hours) and clofibrate (half-life 15 hours) gave similar diurnal triglyceride patterns. The diurnal values were dependent on the fasting values. Changes in the cholesterol/phospholipid ratio during the day may be related to altered post-prandial composition of HDL.
在一项双盲平行试验中,对28名健康志愿者进行了为期10天的治疗,分别给予安慰剂、苯扎贝特(每日3次,每次200毫克)或氯贝丁酯(每日3次,每次500毫克),并测量了他们的昼夜血脂和脂蛋白谱。两种药物均降低了空腹甘油三酯和胆固醇水平(苯扎贝特与安慰剂相比,胆固醇的p值小于或等于0.05)。由于空腹甘油三酯最低,苯扎贝特组的昼夜甘油三酯谱最低。安慰剂组的饮食性血脂异常较轻,是由于极低密度脂蛋白甘油三酯增加所致,而其他脂蛋白脂质和总血浆胆固醇在白天基本保持不变。苯扎贝特(半衰期2小时)和氯贝丁酯(半衰期15小时)呈现出相似的昼夜甘油三酯模式。昼夜值取决于空腹值。白天胆固醇/磷脂比值的变化可能与餐后高密度脂蛋白组成的改变有关。