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环丙贝特和非诺贝特对脂质、脂蛋白以及载脂蛋白A和B影响的比较评估

Comparative evaluation of the effects of ciprofibrate and fenofibrate on lipids, lipoproteins and apoproteins A and B.

作者信息

Rouffy J, Chanu B, Bakir R, Djian F, Goy-Loeper J

出版信息

Atherosclerosis. 1985 Mar;54(3):273-81. doi: 10.1016/0021-9150(85)90121-2.

Abstract

In a double-blind study over a 3-month period, a daily dose of 100 mg ciprofibrate, prescribed in a single administration and a daily dose of 300 mg fenofibrate, prescribed in 3 administrations, significantly reduced the mean values of total cholesterol, LDL cholesterol and VLDL cholesterol, apoprotein B (P less than 0.001) and increased the mean values of HDL cholesterol (P less than 0.01) and total apoprotein A (P less than 0.05). The study, followed-up as an open trial using higher doses (100 or 200 mg/day ciprofibrate, 400 mg/day fenofibrate) tried to demonstrate clearly the benefit of therapy after 9 months with the 2 drugs and to establish the dose-response effects. Comparison of the 2 drugs at the optimal dosages, after 9 months of treatment, showed ciprofibrate to be more effective in increasing HDL cholesterol (P less than 0.05) and apo A (P less than 0.001). No other significant differences in terms of either therapeutic efficacy or biological tolerance became apparent between the 2 drugs. The results obtained in this comparative study were in accordance to those observed in separate trials for ciprofibrate or fenofibrate. Ciprofibrate has the benefit of a long half-life and may also be administered in the form of a single daily dose to patients suffering from major type II hyperlipoproteinaemia.

摘要

在一项为期3个月的双盲研究中,每日单次服用100毫克环丙贝特以及每日分3次服用300毫克非诺贝特,可显著降低总胆固醇、低密度脂蛋白胆固醇和极低密度脂蛋白胆固醇、载脂蛋白B的均值(P<0.001),并提高高密度脂蛋白胆固醇(P<0.01)和总载脂蛋白A的均值(P<0.05)。该研究作为开放试验进行随访,使用更高剂量(环丙贝特100或200毫克/天,非诺贝特400毫克/天),试图明确这两种药物治疗9个月后的益处,并确定剂量反应效应。治疗9个月后,比较两种药物的最佳剂量,结果显示环丙贝特在提高高密度脂蛋白胆固醇(P<0.05)和载脂蛋白A(P<0.001)方面更有效。两种药物在治疗效果或生物耐受性方面没有其他显著差异。该比较研究获得的结果与环丙贝特或非诺贝特单独试验中观察到的结果一致。环丙贝特具有半衰期长的优点,对于患有主要II型高脂蛋白血症的患者,也可以每日单次给药。

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