Perspectives and control of hepatitis B virus infection in Taiwan

被引:70
作者
Lin, Chih-Lin [1 ,2 ]
Kao, Jia-Horng [3 ,4 ,5 ,6 ,7 ]
机构
[1] Taipei City Hosp, Ren Ai Branch, Dept Gastroenterol, Taipei, Taiwan
[2] Natl Chengchi Univ, Dept Psychol, Taipei 11623, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[4] Natl Taiwan Univ, Coll Med, Grad Inst Clin Med, Taipei 10764, Taiwan
[5] Natl Taiwan Univ Hosp, Taipei, Taiwan
[6] Natl Taiwan Univ, Coll Med, Hepatitis Res Ctr, Taipei 10764, Taiwan
[7] Natl Taiwan Univ, Coll Med, Dept Med Res, Taipei 10764, Taiwan
关键词
chronic hepatitis B; HBsAg; HBV DNA; HBV reactivation; hepatocellular carcinoma; risk calculator; PRE-S DELETION; TENOFOVIR DISOPROXIL FUMARATE; TERM ENTECAVIR THERAPY; TO-INFANT TRANSMISSION; HEPATOCELLULAR-CARCINOMA; CORE PROMOTER; NATURAL-HISTORY; VIRAL LOAD; RISK STRATIFICATION; LYMPHOMA PATIENTS;
D O I
10.1016/j.jfma.2015.06.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatitis B virus (HBV) infection is endemic in Taiwan. After the implementation of universal hepatitis B vaccination, there was a significant reduction of hepatitis B surface antigen (HBsAg) seropositivity and HBV-related hepatocellular carcinoma (HCC) incidence in children, teenagers, and young adults. However, the incidence of HBV-related HCC in adults remains high. Through several community-and hospital-based cohort studies, the viral factors affecting the prognosis of HBV carriers have been illustrated. Serum HBV DNA level > 2000 IU/mL at study entry starts to increase the risks of cirrhosis and HCC in adult patients with chronic HBV infection. In addition, serum HBsAg level > 1000 IU/mL is associated with a higher risk of HCC in HBeAg-negative patients with low viral load. Virologically, HBV genotype C/D and core promote/pre-S mutations correlate with an increased HCC risk. Recently, a risk calculator has been developed to predict HCC in noncirrhotic patients with external validation. Therapeutically, hospital-based cohort and population-based nationwide studies indicated that interferon and nucleos(t)ide analogue treatments could reduce the incidence of HCC over time. Towards the ultimate goal of HBV eradication, several novel agents aiming at viral and host targets are under development. In addition, the immune therapy may play a key role in HBV cure in the foreseeable future. Copyright (C) 2015, Elsevier Taiwan LLC & Formosan Medical Association. All rights reserved.
引用
收藏
页码:901 / 909
页数:9
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