Management Strategies for Liver Fibrosis

Стратегии лечения фиброза печени
Alejandra Altamirano-Barrera, Beatriz Barranco-Fragoso, Nahúm Méndez‐Sánchez
2016-12-23

chronic liver injuryhepatic stellate cellshepatitis B and Cliver fibrosisnonalcoholic steatohepatitis
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.
1
Chronic liver injury from viral hepatitis, obesity-related NAFLD/NASH, alcohol, autoimmune hepatitis, and cholangiopathies contributes substantially to liver fibrosis morbidity and mortality.
2
Fibrosis involves recruitment of pro- and anti-inflammatory monocytes and macrophages, along with cytokine and chemokine production.
3
Hepatocyte responses to inflammation play a decisive role in hepatic fibrosis pathophysiology.
4
Inflammatory signaling stimulates hepatic stellate cells and promotes fibrotic progression.
5
Timely detection of liver fibrosis may enable therapeutic intervention to prevent disease progression; the review evaluates available treatment strategies.

liver fibrosis resulting from chronic liver injury

therapeutic management options for liver fibrosis and prevention of its progression, including modulation of inflammation and hepatic stellate cell activation

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2016-12-23
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Alejandra Altamirano-Barrera
Beatriz Barranco-Fragoso
Nahúm Méndez‐Sánchez
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