医学
酒精性肝病
脂肪肝
内科学
比较器
胃肠病学
疾病
物理
电压
量子力学
肝硬化
作者
Manuel Romero‐Gómez,Eric Lawitz,R. Ravi Shankar,Eirum Chaudhri,Jie Liu,Raymond L. H. Lam,Keith D. Kaufman,Samuel S. Engel,Santiago Oscar Bruzone,Maria Jimena Coronel,Fernando Gruz,Ignacio MacKinnon,Jacob George,Kate Muller,Samuel S. Lee,Cyrielle Caussy,Jean‐Michel Petit,Ziv Ben Ari,Marius Braun,Helena Katchman
标识
DOI:10.1016/j.jhep.2023.05.013
摘要
Currently, there are no approved therapies for non-alcoholic steatohepatitis (NASH). The weight loss associated with glucagon-like peptide-1 (GLP-1) receptor agonists has been shown to decrease hepatic inflammation in patients with NASH. In addition to reducing liver fat content (LFC) indirectly through weight loss, glucagon receptor agonism may also reduce LFC by acting on the liver directly to stimulate fatty acid oxidation and reduce lipogenesis. This study demonstrated that treatment of patients with non-alcoholic fatty liver disease with the GLP-1/glucagon receptor co-agonist efinopegdutide (10 mg weekly) led to a significantly greater reduction in LFC compared to treatment with the GLP-1 receptor agonist semaglutide (1 mg weekly), suggesting that efinopegdutide may be an effective treatment for NASH.
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