Are we any closer to treating liver fibrosis (and if no, why not)?

This review provides a personal view on anti-fibrosis therapy in the liver. The worst clinical consequence of liver fibrosis is the development of liver cirrhosis and portal hypertension. Etiology is a decisive factor which determines patterns of fibrous septa and subsequent vascular remodeling, whi...

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Bibliographic Details
Main Authors: Feng, Rilu (Author) , Yuan, Xiaodong (Author) , Weng, Honglei (Author)
Format: Article (Journal)
Language:English
Published: 01 February 2018
In: Journal of digestive diseases
Year: 2018, Volume: 19, Issue: 3, Pages: 118-126
ISSN:1751-2980
DOI:10.1111/1751-2980.12584
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1111/1751-2980.12584
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/1751-2980.12584
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Author Notes:Rilu Feng, Xiaodong Yuan, Chen Shao, Huiguo Ding, Roman Liebe and Hong-Lei Weng
Description
Summary:This review provides a personal view on anti-fibrosis therapy in the liver. The worst clinical consequence of liver fibrosis is the development of liver cirrhosis and portal hypertension. Etiology is a decisive factor which determines patterns of fibrous septa and subsequent vascular remodeling, which is essential for the development of portal hypertension. Removing or controlling the disease-causing agent, i.e. anti-viral treatment for hepatitis, is the essential first step for treating chronic liver diseases and can reverse fibrosis in some settings. However, removing etiology is not always sufficient to prevent fibrosis from progressing towards cirrhosis and portal hypertension. In liver diseases such as severe alcoholic hepatitis and massive parenchymal loss, the formation of vascular anastomoses between portal to central veins based on bridging fibrosis results in cirrhosis and portal hypertension. For these patients, anti-fibrotic treatment is crucial and urgent. Unfortunately, a lack of understanding how fibrosis contributes to vascular remodeling caused by and combined with a lack of suitable experimental models that recapitulate human liver diseases, has hampered the development of successful anti-fibrotic drugs for clinical use to date.
Item Description:Gesehen am 10.06.2020
Physical Description:Online Resource
ISSN:1751-2980
DOI:10.1111/1751-2980.12584