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Clinical use of liver biopsy for the diagnosis and management of inactive and asymptomatic hepatitis B virus carriers in Bangladesh
Author(s) -
AlMahtab Mamun,
Rahman Salimur,
Akbar Sheikh Mohammad Fazle,
Kamal Mohammad,
Khan Mohammad Sakirul Islam
Publication year - 2010
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.21830
Subject(s) - asymptomatic , virology , medicine , liver biopsy , asymptomatic carrier , hepatitis b virus , virus , biopsy , pathology
Patients with inactive chronic hepatitis B virus (HBV) infection are assumed to be free from liver disease. Accordingly, antiviral drug treatment is not recommended for these patients. However, the extent of liver damage in these patients has not been evaluated fully. The aim of this study was to evaluate the extent of liver damage in patients with inactive HBV. Liver biopsy was conducted in 141 inactive HBV carriers [HBeAg‐negative, low levels of HBV DNA (≤10,000 copies/ml) and normal levels of serum alanine aminotransferase (ALT)]. The extent of hepatic inflammation and fibrosis was evaluated in these patients by examining liver biopsy specimens. Although the patients were inactive HBV carriers, mild to moderate levels of necroinflammation (HAI necroinflammation score HAI‐N1 ≥ 7) were detected in 36 of 141 (26%) patients. Seventeen patients had a severe degree of hepatic fibrosis (HAI fibrosis score HAI‐F ≥ 3). A total of 10 patients had both considerable necroinflammation (HAI‐N1≥7) and severe fibrosis (HAI‐F ≥3). All 10 patients with significant hepatic inflammation and fibrosis were male and older than 25 years. However, all were HBeAg‐negative and expressed low levels of HBV DNA and normal ALT levels. The study demonstrates that features of liver damage were present in a considerable number of the patients. Assessment of liver biopsy specimens in a larger cohort of inactive HBV carriers is necessary to establish management guidelines for such patients. J. Med. Virol. 82:1350–1354, 2010. © 2010 Wiley‐Liss, Inc.