Management Strategies for Liver Fibrosis

被引:203
作者
Altamirano-Barrera, Alejandra [1 ]
Barranco-Fragoso, Beatriz [2 ]
Mendez-Sanchez, Nahum [1 ]
机构
[1] Med Sur Clin & Fdn, Liver Res Unit, Puente Piedra 150, Mexico City 14050, DF, Mexico
[2] Natl Med Ctr 20 Noviembre, Dept Gastroenterol, Mexico City 03229, DF, Mexico
关键词
Liver fibrosis; Cirrhosis; NASH; Viral hepatitis; Autoimmune liver diseases; EXPERIMENTAL HEPATIC-FIBROSIS; HEPATOCYTE GROWTH-FACTOR; BILE-ACID METABOLISM; URSODEOXYCHOLIC ACID; STELLATE CELLS; CAFFEINE CONSUMPTION; IMATINIB MESYLATE; GENE-EXPRESSION; PIRFENIDONE; INJURY;
D O I
10.5604/16652681.1226814
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Liver fibrosis resulting from chronic liver injury are major causes of morbidity and mortality worldwide. Among causes of hepatic fibrosis, viral infection is most common (hepatitis B and C). In addition, obesity rates worldwide have accelerated the risk of liver injury due to nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). Also liver fibrosis is associated with the consumption of alcohol, or autoimmune hepatitis and chronic cholangiophaties. The response of hepatocytes to inflammation plays a decisive role in the physiopathology of hepatic fibrosis, which involves the recruitment of both pro- and anti-inflammatory cells such as monocytes and macrophages. As well as the production of other cytokines and chemokines, which increase the stimulus of hepatic stellate cells by activating proinflammatory cells. The aim of this review is to identify the therapeutic options available for the treatment of the liver fibrosis, enabling the prevention of progression when is detected in time.
引用
收藏
页码:48 / 56
页数:9
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