Fatty liver and FGF21 physiology

被引:48
|
作者
Maratos-Flier, Eleftheria [1 ]
机构
[1] Harvard Med Sch, Dept Med, Div Endocrinol, Beth Israel Deaconess Med Ctr, CLS 7 3 Blackfan Circle, Boston, MA 02215 USA
关键词
Non-alcoholic fatty liver disease; FGF21; Obesity; Metabolic syndrome; Insulin resistance; GROWTH-FACTOR; 21; BROWN ADIPOSE-TISSUE; INSULIN-RESISTANCE; HEPATIC STEATOSIS; CIRCULATING FGF21; KETOGENIC DIET; UNITED-STATES; PPAR-ALPHA; DISEASE; OBESITY;
D O I
10.1016/j.yexcr.2017.05.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non alcoholic fatty liver disease is linked to obesity and the metabolic syndrome. As rates of obesity rise it has become the major etiology of liver dysfunction. Despite intense study the molecular mechanisms contributing to the onset of fatty liver remain debatable. Furthermore, few therapies exist and as a result dietary therapy is commonly prescribed and remains problematic. Fibroblast growth factor is a complex metabolic regulator that is synthesized in multiple organs including the liver, with resulting complex systemic effects. Several lines of evidence suggest that effects in the liver lead to decreased fat accumulation and that treatment results in reduced inflammation and fibrosis. Understanding the physiology of FGF21 is important to the understanding of liver disease and may also provide targets for future therapy.
引用
收藏
页码:2 / 5
页数:4
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