Treatment of hyperlipoproteinemia type II with etofibrate.

A Gustafson
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Abstract

Seven patients with hyperlipoproteinemia (HLP) type II (four patients with type II A and three patients with type II B), who were experienced to be resistant to hypolipidemic drugs, were treated for 6 months with etofibrate, a double-ester of nicotinic acid and clofibrinic acid, at a dose of 0.3 g t.i.d. Mean serum cholesterol level decreased by up to 18% from a pre-treatment value of 7.7 +/- 1.4 mmol/l. The reduction of serum cholesterol was due both to a decrease in very low density (VLDL) and low density (LDL) lipoprotein cholesteral by 61 and 25%, respectively (after 6 months). Furthermore alpha-LP (HDL) cholesterol increased by 8%, (after 6 months). All seven patients had previously received clofibrate and had obtained a mean decrease in plasma cholesterol by 6%. There was a slight transient increase in S-ASAT and S-ALAT simultaneous with in increase in serum urate. However, these values returned after 3 months to pre-treatment level. No influence on glucose tolerance was recorded. There were no bothersome side effects except a transient discomfort in the form of flushing or acid indigestion which occurred after 1--2 months of treatment with etofibrate.

依妥贝特治疗II型高脂蛋白血症。
7例II型高脂蛋白血症(HLP)患者(4例ⅱA型患者和3例ⅱB型患者)对降血脂药物有耐药性,用依托贝特治疗6个月,依托贝特是一种烟酸和氯纤维素酸的双酯,剂量为0.3 g / d。平均血清胆固醇水平比治疗前的7.7 +/- 1.4 mmol/l下降了18%。血清胆固醇的降低是由于极低密度(VLDL)和低密度(LDL)脂蛋白胆固醇分别降低了61%和25%(6个月后)。此外,α - lp (HDL)胆固醇增加了8%(6个月后)。所有7名患者之前都接受过氯贝特治疗,血浆胆固醇平均下降了6%。S-ASAT和S-ALAT在血清尿酸升高的同时有短暂的轻微升高。然而,这些值在3个月后恢复到治疗前的水平。对葡萄糖耐量无影响。除了使用依妥贝特治疗1- 2个月后出现短暂的潮红或酸性消化不良外,没有令人烦恼的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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