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Use of the thyroid hormone analogue eprotirome in statin-treated dyslipidemia.

机译:在他汀类药物治疗的血脂异常中使用甲状腺激素类似物蛋白血症。

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BACKGROUND: Dyslipidemia increases the risk of atherosclerotic cardiovascular disease and is incompletely reversed by statin therapy alone in many patients. Thyroid hormone lowers levels of serum low-density lipoprotein (LDL) cholesterol and has other potentially favorable actions on lipoprotein metabolism. Consequently, thyromimetic drugs hold promise as lipid-lowering agents if adverse effects can be avoided. METHODS: We performed a randomized, placebo-controlled, double-blind, multicenter trial to assess the safety and efficacy of the thyromimetic compound eprotirome (KB2115) in lowering the level of serum LDL cholesterol in patients with hypercholesterolemia who were already receiving simvastatin or atorvastatin. In addition to statin treatment, patients received either eprotirome (at a dose of 25, 50, or 100 microg per day) or placebo. Secondary outcomes were changes in levels of serum apolipoprotein B, triglycerides, and Lp(a) lipoprotein. Patients were monitored for potential adverse thyromimetic effects on the heart, bone, and pituitary. RESULTS: The addition of placebo or eprotirome at a dose of 25, 50, or 100 microg daily to statin treatment for 12 weeks reduced the mean level of serum LDL cholesterol from 141 mg per deciliter (3.6 mmol per liter) to 127, 113, 99, and 94 mg per deciliter (3.3, 2.9, 2.6, and 2.4 mmol per liter), respectively, (mean reduction from baseline, 7%, 22%, 28%, and 32%). Similar reductions were seen in levels of serum apolipoprotein B, triglycerides, and Lp(a) lipoprotein. Eprotirome therapy was not associated with adverse effects on the heart or bone. No change in levels of serum thyrotropin or triiodothyronine was detected, although the thyroxine level decreased in patients receiving eprotirome. CONCLUSIONS: In this 12-week trial, the thyroid hormone analogue eprotirome was associated with decreases in levels of atherogenic lipoproteins in patients receiving treatment with statins. (ClinicalTrials.gov number, NCT00593047.)
机译:背景:血脂异常会增加动脉粥样硬化性心血管疾病的风险,在许多患者中,仅通过他汀类药物疗法就不能完全逆转血脂异常。甲状腺激素可降低血清低密度脂蛋白(LDL)胆固醇的水平,并对脂蛋白代谢具有其他潜在的有利作用。因此,如果可以避免不良反应,则拟甲状腺激素药物有望作为降血脂药。方法:我们进行了一项随机,安慰剂对照,双盲,多中心试验,以评估拟甲状腺激素复合疗法(KB2115)在降低已经接受辛伐他汀或阿托伐他汀治疗的高胆固醇血症患者中降低血清LDL胆固醇水平的安全性和有效性。 。除他汀类药物治疗外,患者还接受了eprotirome(每天25、50或100微克的剂量)或安慰剂。次要结果是血清载脂蛋白B,甘油三酸酯和Lp(a)脂蛋白水平的变化。监测患者对心脏,骨骼和垂体的潜在不良甲状腺功能。结果:在他汀类药物治疗中连续12周每天服用剂量为25、50或100微克的安慰剂或催眠药后,血清LDL胆固醇的平均水平从141毫克/分升(3.6毫摩尔/升)降至127、113,每分升分别为99和94 mg(每升分别为3.3、2.9、2.6和2.4 mmol)(相对于基线的平均减少量为7%,22%,28%和32%)。血清载脂蛋白B,甘油三酸酯和Lp(a)脂蛋白的水平也有类似的下降。激素疗法与对心脏或骨骼的不良影响无关。尽管接受厄普罗替尼治疗的患者甲状腺素水平降低,但未检测到血清促甲状腺激素或三碘甲状腺素水平的变化。结论:在这项为期12周的试验中,接受他汀类药物治疗的患者中,甲状腺激素类似物致蛋白血症与动脉粥样硬化脂蛋白水平降低有关。 (ClinicalTrials.gov编号,NCT00593047。)

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