Karim Gres, Bansal Meena B
Department of Medicine, Mount Sinai Israel, New York, NY, USA.
Division of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
touchREV Endocrinol. 2023 May;19(1):60-70. doi: 10.17925/EE.2023.19.1.60. Epub 2023 May 1.
Non-alcoholic fatty liver disease (NAFLD) encompasses a spectrum of fatty liver disease, including non-alcoholic fatty liver (NAFL) and its more progressive form, non-alcoholic steatohepatitis (NASH). The prevalence of NAFLD/NASH along with type 2 diabetes and obesity is rising worldwide. In those who develop NASH, unlike those with bland steatosis (NAFL), lipotoxic lipids drive hepatocyte injury, inflammation and stellate cell activation leading to progressive accumulation of collagen or fibrosis, ultimately leading to cirrhosis and increased risk of hepatocellular carcinoma. Hypothyroidism is associated with NAFLD/NASH; specifically, intrahepatic hypothyroidism drives lipotoxicty in preclinical models. Agonists of thyroid hormone receptor (THR)-β, which is primarily found in the liver, can promote lipophagy, mitochondrial biogenesis and mitophagy, stimulating increased hepatic fatty acid β-oxidation, and thereby decreasing the burden of lipotoxic lipids, while promoting low-density lipoprotein (LDL) uptake and favourable effects on lipid profiles. A number of THR-β agonists are currently being investigated for NASH. This review focuses on resmetirom, an orally administered, once-daily, small-molecule, liver-directed, ß-selective THR agonist, as it is furthest along in development. Data from completed clincal studies outlined in this review demonstrate that resmetirom is effective in reducing hepatic fat content as measured by magnetic resonance imaging-derived proton density fat fraction, reduces liver enzymes, improves non-i nvasive markers of liver fibrogenesis and decreases liver stiffness, while eliciting a favourable cardiovascular profile with a reduction in serum lipids, including LDL cholesterol. Topline phase III biopsy data showed resolution of NASH and/or fibrosis improvement after 52 weeks of treatment, with more detailed peer-reviewed findings anticipated in order to certify these findings. Longer term clinical outcomes from both MAESTRO-NASH and MAESTRO-NASH OUTCOMES will be a pivotal juncture in the drug's road towards being approved as a NASH therapeutic.
非酒精性脂肪性肝病(NAFLD)涵盖一系列脂肪性肝病,包括非酒精性脂肪肝(NAFL)及其更进展的形式,非酒精性脂肪性肝炎(NASH)。全球范围内,NAFLD/NASH与2型糖尿病和肥胖症的患病率都在上升。在发生NASH的患者中,与单纯性脂肪变性(NAFL)患者不同,脂毒性脂质会导致肝细胞损伤、炎症和星状细胞激活,进而导致胶原蛋白或纤维化逐渐积累,最终导致肝硬化并增加肝细胞癌风险。甲状腺功能减退与NAFLD/NASH相关;具体而言,肝内甲状腺功能减退在临床前模型中会引发脂毒性。主要在肝脏中发现的甲状腺激素受体(THR)-β激动剂可促进脂肪自噬、线粒体生物合成和线粒体自噬,刺激肝脏脂肪酸β氧化增加,从而减轻脂毒性脂质负担,同时促进低密度脂蛋白(LDL)摄取并对脂质谱产生有利影响。目前正在对多种THR-β激动剂进行NASH研究。本综述重点关注瑞美替昂,这是一种口服、每日一次的小分子、肝脏靶向、β选择性THR激动剂,因为它在研发中进展最为领先。本综述中概述的已完成临床研究数据表明,瑞美替昂可有效降低通过磁共振成像衍生的质子密度脂肪分数测量的肝脏脂肪含量,降低肝酶,改善肝脏纤维化的非侵入性标志物并降低肝脏硬度,同时在降低包括LDL胆固醇在内的血脂方面呈现出有利的心血管特征。III期活检的主要数据显示,治疗52周后NASH得到缓解和/或纤维化改善,预计将有更详细的同行评审结果来证实这些发现。MAESTRO-NASH和MAESTRO-NASH OUTCOMES的长期临床结果将是该药物获批成为NASH治疗药物道路上的关键转折点。