Department of Endocrinology, Metabolism and Diabetes, Center for Biosciences, Karolinska Institutet At Karolinska University Hospital Huddinge, Stockholm, Sweden.
Center for Biosciences, Department of Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, Stockholm, Sweden.
J Intern Med. 2015 Mar;277(3):331-342. doi: 10.1111/joim.12261. Epub 2014 May 16.
Liver-selective thyromimetic agents could provide a new approach for treating dyslipidaemia.
We performed a multicentre, randomized, placebo-controlled, double-blind study to evaluate the efficacy and safety of eprotirome, a liver-selective thyroid hormone receptor agonist, in 98 patients with primary hypercholesterolaemia. After previous drug wash-out and dietary run-in, patients received 100 or 200 μg day(-1) eprotirome or placebo for 12 weeks. The primary end-point was change in serum LDL cholesterol; secondary end-points included changes in other lipid parameters and safety measures.
Eprotirome treatment at 100 and 200 μg daily reduced serum LDL cholesterol levels by 23 ± 5% and 31 ± 4%, respectively, compared with 2 ± 6% for placebo (P < 0.0001). Similar reductions were seen in non-HDL cholesterol and apolipoprotein (apo) B, whereas serum levels of HDL cholesterol and apo A-I were unchanged. There were also considerable reductions in serum triglycerides and lipoprotein(a), in particular in patients with elevated levels at baseline. There was no evidence of adverse effects on heart or bone and no changes in serum thyrotropin or triiodothyronine, although the thyroxine level decreased. Low-grade increases in liver enzymes were evident in most patients.
In hypercholesterolaemic patients, the liver-selective thyromimetic eprotirome decreased serum levels of atherogenic lipoproteins without signs of extra-hepatic side effects. Selective stimulation of hepatic thyroid hormone receptors may be an attractive way to modulate lipid metabolism in hyperlipidaemia.
肝选择性甲状腺激素类似物可能为治疗血脂异常提供一种新的方法。
我们进行了一项多中心、随机、安慰剂对照、双盲研究,以评估肝选择性甲状腺激素受体激动剂 eprotirome 在 98 例原发性高胆固醇血症患者中的疗效和安全性。在药物洗脱和饮食适应期后,患者接受 100 或 200μg/天 eprotirome 或安慰剂治疗 12 周。主要终点为血清 LDL 胆固醇的变化;次要终点包括其他脂质参数和安全性措施的变化。
eprotirome 治疗 100 和 200μg/天分别使血清 LDL 胆固醇水平降低 23±5%和 31±4%,安慰剂组为 2±6%(P<0.0001)。非高密度脂蛋白胆固醇和载脂蛋白(apo)B 也有类似的降低,而高密度脂蛋白胆固醇和 apoA-I 水平不变。血清甘油三酯和脂蛋白(a)也有显著降低,特别是在基线时升高的患者。没有证据表明对心脏或骨骼有不良影响,血清促甲状腺激素或三碘甲状腺原氨酸也没有变化,尽管甲状腺素水平下降。大多数患者的肝酶有轻度升高。
在高胆固醇血症患者中,肝选择性甲状腺激素类似物 eprotirome 降低了致动脉粥样硬化脂蛋白的血清水平,没有肝外副作用的迹象。选择性刺激肝甲状腺激素受体可能是调节高脂血症中脂质代谢的一种有吸引力的方法。