Clinical evidence for the regression of liver fibrosis

被引:383
作者
Ellis, Elizabeth L. [1 ]
Mann, Derek A. [1 ]
机构
[1] Newcastle Univ, Sch Med, Fibrosis Lab, Inst Cellular Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
PRIMARY BILIARY-CIRRHOSIS; SUSTAINED VIROLOGICAL RESPONSE; CHRONIC HEPATITIS-C; RANDOMIZED CONTROLLED-TRIAL; VENOUS-PRESSURE GRADIENT; HEPATOCELLULAR-CARCINOMA; INTERFERON-ALPHA; FOLLOW-UP; GENETIC HEMOCHROMATOSIS; WILSON DISEASE;
D O I
10.1016/j.jhep.2011.09.024
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Fibrosis is a common pathological process for the majority of liver diseases which in a significant minority of patients leads to end-stage cirrhosis and/or hepatocellular carcinoma. Data emerging from small rodent models of chronic liver disease have demonstrated that fibrotic extracellular matrix can be remodelled and near-normal hepatic architecture regenerated upon cessation of injury. Moreover, regression of liver fibrosis in these model systems can be stimulated with drugs that target the activities of fibrogenic hepatic stellate cells. These findings are exciting as they suggest that established fibrosis is susceptible to regression and possibly even reversion. Alongside these experimental studies is a growing body of clinical data that suggest regression of fibrosis may also occur in liver disease patients for whom an effective treatment is available for their underlying liver injury. This paper provides an up-to-date review of the currently available clinical data and also considers technical caveats that highlight the need for caution in establishing a new dogma that human liver fibrosis is reversible. (C) 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1171 / 1180
页数:10
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