Delitala Alessandro P, Delitala Giuseppe, Sioni Paolo, Fanciulli Giuseppe
a Azienda Ospedaliero-Universitaria di Sassari , Sassari , Italy.
b Department of Clinical and Experimental Medicine , University of Sassari , Sassari , Italy.
Curr Med Res Opin. 2017 Nov;33(11):1985-1993. doi: 10.1080/03007995.2017.1330259. Epub 2017 Jun 9.
Treatment of dyslipidemia is a major burden for public health. Thyroid hormone regulates lipid metabolism by binding the thyroid hormone receptor (TR), but the use of thyroid hormone to treat dyslipidemia is not indicated due to its deleterious effects on heart, bone, and muscle. Thyroid hormone analogs have been conceived to selectively activate TR in the liver, thus reducing potential side-effects.
The authors searched the PubMed database to review TR and the action of thyromimetics in vitro and in animal models. Then, all double-blind, placebo controlled trials that analyzed the use of thyroid hormone analog for the treatment of dyslipidemia in humans were included. Finally, the ongoing research on the use of TR agonists was searched, searching the US National Institutes of Health Registry and the WHO International Clinical Trial Registry Platform (ICTRP).
Thyromimetics were tested in humans for the treatment of dyslipidemia, as a single therapeutic agent or as an add-on therapy to the traditional lipid-lowering drugs. In most trials, thyromimetics lowered total cholesterol, low-density lipoprotein cholesterol, and triglycerides, but their use has been associated with adverse side-effects, both in pre-clinical studies and in humans.
The use of thyromimetics for the treatment of dyslipidemia is not presently recommended. Future possible clinical applications might include their use to promote weight reduction. Thyromimetics might also represent an interesting alternative, both for the treatment of non-alcoholic steatohepatitis, and type 2 diabetes due to their positive effects on insulin sensitivity. Finally, additional experimental and clinical studies are needed for a better comprehension of the effect(s) of a long-term therapy.
血脂异常的治疗是公共卫生的一项重大负担。甲状腺激素通过与甲状腺激素受体(TR)结合来调节脂质代谢,但由于其对心脏、骨骼和肌肉的有害影响,不建议使用甲状腺激素来治疗血脂异常。甲状腺激素类似物被设想为可在肝脏中选择性激活TR,从而减少潜在的副作用。
作者检索了PubMed数据库,以综述TR及甲状腺激素模拟物在体外和动物模型中的作用。然后,纳入了所有分析甲状腺激素类似物用于治疗人类血脂异常的双盲、安慰剂对照试验。最后,检索了关于使用TR激动剂的正在进行的研究,搜索了美国国立卫生研究院注册库和世界卫生组织国际临床试验注册平台(ICTRP)。
甲状腺激素模拟物作为单一治疗剂或作为传统降脂药物的附加疗法,在人类中进行了血脂异常治疗的测试。在大多数试验中,甲状腺激素模拟物降低了总胆固醇、低密度脂蛋白胆固醇和甘油三酯,但在临床前研究和人类研究中,其使用都与不良副作用相关。
目前不推荐使用甲状腺激素模拟物治疗血脂异常。未来可能的临床应用可能包括用于促进体重减轻。由于甲状腺激素模拟物对胰岛素敏感性有积极影响,它们也可能是治疗非酒精性脂肪性肝炎和2型糖尿病的一个有趣替代方案。最后,需要更多的实验和临床研究来更好地理解长期治疗的效果。