Hepatitis B-associated fibrosis and fibrosis/cirrhosis regression with nucleoside and nucleotide analogs

被引:3
作者
Brown, Ashley [1 ]
Goodman, Zachary [2 ]
机构
[1] Imperial Coll Healthcare NHS Trust, Dept Hepatol, London, England
[2] Inova Fairfax Hosp, Ctr Liver Dis, Falls Church, VA 22042 USA
关键词
adefovir; chronic hepatitis B; cirrhosis; entecavir; fibrosis; hepatitis B virus; lamivudine; telbivudine; tenofovir; TENOFOVIR DISOPROXIL FUMARATE; ADEFOVIR DIPIVOXIL; LIVER FIBROSIS; HEPATOCELLULAR-CARCINOMA; HBV-DNA; ENTECAVIR TREATMENT; PORTAL PRESSURE; IMAGE-ANALYSIS; BLOOD-TESTS; VIRAL LOAD;
D O I
10.1586/EGH.12.4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis B virus (HBV) infection currently accounts for approximately 600,000 deaths per year resulting from progression of liver fibrosis to cirrhosis and hepatocellular carcinoma. Treatment of chronic hepatitis B with antiviral agents aims to improve survival through the reduction of HBV DNA to undetectable levels and the resultant prevention of disease progression. In recent years, observations in various disease areas have shown that liver fibrosis can be reversed if the underlying cause of the liver damage is effectively addressed. In line with these observations, there is now considerable evidence to suggest that effective sustained suppression of HBV replication with long-term anti-HBV treatment can result in measurable improvements in liver fibrosis over time, even in patients with advanced cirrhosis. This review article provides an overview of currently available data on regression of fibrosis and cirrhosis in patients with chronic hepatitis B treated with nucleoside and nucleotide analog inhibitors of HBV.
引用
收藏
页码:187 / 198
页数:12
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