Service of Endocrinology, Diabetes, Nutrition and Therapeutic Patient Education, Geneva University Hospitals, 1211 Geneva, Switzerland.
Diabetes Center of the Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Int J Mol Sci. 2021 Nov 26;22(23):12797. doi: 10.3390/ijms222312797.
Thyroid hormones control lipid metabolism by exhibiting specific effects on the liver and adipose tissue in a coordinated manner. Different diseases of the thyroid gland can result in hypothyroidism. Hypothyroidism is frequently associated with dyslipidemia. Hypothyroidism-associated dyslipidemia subsequently results in intrahepatic accumulation of fat, leading to nonalcoholic fatty liver disease (NAFLD), which leads to the development of hepatic insulin resistance. The prevalence of NAFLD in the western world is increasing, and evidence of its association with hypothyroidism is accumulating. Since hypothyroidism has been identified as a modifiable risk factor of NAFLD and recent data provides evidence that selective thyroid hormone receptor β (THR-β) agonists are effective in the treatment of dyslipidemia and NAFLD, interest in potential therapeutic options for NAFLD targeting these receptors is growing. In this review, we summarize current knowledge regarding clinical and molecular data exploring the association of hypothyroidism, dyslipidemia and NAFLD.
甲状腺激素通过对肝脏和脂肪组织表现出特定的协同作用来控制脂质代谢。甲状腺的不同疾病可导致甲状腺功能减退症。甲状腺功能减退症常与血脂异常有关。甲状腺功能减退症相关的血脂异常随后导致肝内脂肪堆积,导致非酒精性脂肪性肝病(NAFLD),从而导致肝胰岛素抵抗。NAFLD 在西方国家的患病率正在增加,并且有越来越多的证据表明其与甲状腺功能减退症有关。由于甲状腺功能减退症已被确定为 NAFLD 的可改变危险因素,并且最近的数据提供了证据表明,选择性甲状腺激素受体 β(THR-β)激动剂对治疗血脂异常和 NAFLD 有效,因此,人们对针对这些受体的 NAFLD 潜在治疗方法的兴趣正在增加。在这篇综述中,我们总结了有关探索甲状腺功能减退症、血脂异常和 NAFLD 之间关联的临床和分子数据的最新知识。