Schwartzkopff W, Russ E
MMW Munch Med Wochenschr. 1975 May 9;117(19):827-30.
The effect of etiroxate and dextrothyroxine (CT4) on lipoproteins was determined in a long-term study comprising 40 patients with Type IIa hyperlipoproteinaemia and 19 patients with Type IIb. 40 mg etiroxate daily lowered the total lipids, phosphatides, cholesterol, and beta-lipoproteins more significantly than 6 mg DT4/day. After the administration of etiroxate and DT4, cholesterol decreased by 17.9% and 14.5% respectively in Type IIa and 16.6% and 12.6% respectively in Type IIb. The mean decrease in the beta-lipoproteins after etiroxate was 134 plus or minus 75 mg/100 ml in Type IIa and 96 plus or minus 101 mg/100 ml in Type IIb, and after DT495 plus or minus 69 mg/100 ml in Type IIa and 79 plus or minus 58 mg/100 ml in Type IIb. Transient gastric intolerance occurred after both drugs. In susceptible patients cardiac side effects were more frequently observed after DT4 than after etiroxate, but there was no statistical difference between the two drugs or the placebo phase.
在一项长期研究中,对40例IIa型高脂蛋白血症患者和19例IIb型患者测定了依托沙酯和右旋甲状腺素(CT4)对脂蛋白的影响。每日服用40mg依托沙酯比每日服用6mg DT4能更显著地降低总脂质、磷脂、胆固醇和β-脂蛋白。服用依托沙酯和DT4后,IIa型患者的胆固醇分别下降了17.9%和14.5%,IIb型患者分别下降了16.6%和12.6%。依托沙酯治疗后,IIa型患者β-脂蛋白的平均下降幅度为134±75mg/100ml,IIb型患者为96±101mg/100ml;DT4治疗后,IIa型患者为95±69mg/100ml,IIb型患者为79±58mg/100ml。两种药物服用后均出现短暂的胃部不耐受。在易感患者中,DT4治疗后比依托沙酯治疗后更频繁地观察到心脏副作用,但两种药物与安慰剂阶段之间没有统计学差异。