The future of incretins in the treatment of obesity and non-alcoholic fatty liver disease

被引:21
作者
Andreasen, Christine R. [1 ,2 ]
Andersen, Andreas [1 ,2 ]
Vilsboll, Tina [1 ,2 ,3 ]
机构
[1] Copenhagen Univ Hosp, Steno Diabet Ctr Copenhagen, Clin Res, Herlev, Denmark
[2] Univ Copenhagen, Gentofte Hosp, Ctr Clin Metab Res, Hellerup, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
关键词
Glucagon-like peptide-1; Glucose-dependent insulinotropic polypeptide; Incretins; Non-alcoholic fatty liver disease; Obesity; Review; GLUCAGON-LIKE PEPTIDE-1; SEMAGLUTIDE; 2.4; MG; DOUBLE-BLIND; WEIGHT MANAGEMENT; INSULIN-RESISTANCE; RECEPTOR AGONISTS; CORRECTS OBESITY; SCORING SYSTEM; ADIPOSE-TISSUE; DOUBLE-DUMMY;
D O I
10.1007/s00125-023-05966-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the last few decades, glucagon-like peptide-1 receptor (GLP-1R) agonists have changed current guidelines and improved outcomes for individuals with type 2 diabetes. However, the dual glucose-dependent insulinotropic polypeptide receptor (GIPR)/GLP-1R agonist, tirzepatide, has demonstrated superior efficacy regarding improvements in HbA(1c) and body weight in people with type 2 diabetes. This has led to increasing scientific interest in incretin hormones and incretin interactions, and several compounds based on dual- and multi-agonists are now being investigated for the treatment of metabolic diseases. Herein, we highlight the key scientific advances in utilising incretins for the treatment of obesity and, potentially, non-alcoholic fatty liver disease (NAFLD). The development of multi-agonists with multi-organ targets may alter the natural history of these diseases.
引用
收藏
页码:1846 / 1858
页数:13
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