Mechanism and prediction of HCC development in HBV infection

被引：34

作者：

Xu, Weiqi ^{[1
]}

Yu, Jun ^{[1
,2
]}

Wong, Vincent Wai-Sun ^{[1
,2
]}

机构：

[1] Chinese Univ Hong Kong, State Key Lab Digest Dis, Hong Kong, Hong Kong, Peoples R China

[2] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China

来源：

BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY | 2017年 / 31卷 / 03期

关键词：

Hepatocellular carcinoma; Liver cirrhosis; Liver fibrosis; Chronic hepatitis B; Entecavir; HEPATITIS-B-VIRUS; HEPATOCELLULAR-CARCINOMA DEVELOPMENT; GENOME-WIDE ASSOCIATION; X PROTEIN; LIVER FIBROSIS; TRANSIENT ELASTOGRAPHY; RISK SCORES; NONINVASIVE ASSESSMENT; STIFFNESS MEASUREMENT; MUTATIONAL LANDSCAPE;

D O I：

10.1016/j.bpg.2017.04.011

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Chronic hepatitis B virus (HBV) infection remains one of the leading causes of hepatocellular carcinoma (HCC) globally. Over the past few decades, the risk factors of HCC in patients with chronic hepatitis B have been well characterized, and can be divided into host and viral factors. A few groups have also derived and validated HCC prediction scores based on these risk factors. In general, the scores have high negative predictive value in identifying a low risk group who may not need HCC surveillance in the next 3-5 years. The scores have been tested originally in Asian patients, and results on their performance in the Caucasian population are conflicting. Furthermore, new research has identified genetic factors and new virological markers (e.g. hepatitis B surface antigen and core-related antigen levels) for HCC, but they are yet to be applied in routine clinical practice. (C) 2017 Elsevier Ltd. All rights reserved.

引用

页码：291 / 298

页数：8

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