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Hepatitis B e antigen–negative chronic hepatitis b in Hong Kong

dc.contributor.authorChan, Henry L. Y.en_US
dc.contributor.authorLeung, Nancy W. Y.en_US
dc.contributor.authorHussain, Munira T.en_US
dc.contributor.authorWong, May L.en_US
dc.contributor.authorLok, Anna Suk-Fongen_US
dc.date.accessioned2006-04-19T13:49:58Z
dc.date.available2006-04-19T13:49:58Z
dc.date.issued2000-03en_US
dc.identifier.citationChan, Henry L. Y.; Leung, Nancy W. Y.; Hussain, Munira; Wong, May L.; Lok, Anna S. F. (2000)."Hepatitis B e antigen–negative chronic hepatitis b in Hong Kong." Hepatology 31(3): 763-768. <http://hdl.handle.net/2027.42/34778>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34778
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10706570&dopt=citationen_US
dc.description.abstractHepatitis B e antigen–negative chronic hepatitis B (e−CHB) has been reported in Asia but its prevalence and clinical significance have not been determined. The aims of this study were to determine the prevalence of e−CHB in Hong Kong and the frequency of precore and core promoter mutations in these patients. A cross-sectional study was performed in 350 consecutive Chinese patients (230 men and 120 women; mean age ±SD, 42 ± 13 years) with chronic hepatitis B virus infection. A total of 243 (69%) patients were hepatitis B e antigen (HBeAg)-negative of whom 15% had clinical cirrhosis. In the remaining 85% of patients, 63% had normal and 22% had elevated transaminases. Serum hepatitis B virus (HBV) DNA was detectable using branched DNA assay in 46% of HBeAg-negative patients with clinical cirrhosis/elevated transaminases. Forty-five percent of the patients with e−CHB had the precore stop codon mutation, and an additional 41% had core promoter changes. There was no correlation between the presence of precore/core promoter mutations and liver disease or HBV-DNA levels. Overall, 17% of HBeAg-negative patients were viremic and had evidence of chronic liver disease (e−CHB) with mean HBV-DNA levels comparable with that in HBeAg-positive patients. In summary, we found that e−CHB may be present in up to 17% of HBeAg-negative patients seen in a tertiary referral center in Hong Kong. e−CHB may be a heterogenous condition and is not invariably associated with the precore HBV mutant. Population studies are needed to determine the true prevalence of e−CHB in Asia and to assess its natural course and response to treatment.en_US
dc.format.extent82691 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherW.B. Saundersen_US
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleHepatitis B e antigen–negative chronic hepatitis b in Hong Kongen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan and VA Medical Center, Ann Arbor, MI ; Division of Gastroenterology and Hepatology, Prince of Wales Hospital, Hong Kong SAR, Chinaen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan and VA Medical Center, Ann Arbor, MIen_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan and VA Medical Center, Ann Arbor, MI ; Division of Gastroenterology, University of Michigan Medical Center, 3912 Taubman Center, Box 0362, Ann Arbor, MI 48109. fax: 734-936-7392en_US
dc.contributor.affiliationotherDivision of Gastroenterology and Hepatology, Prince of Wales Hospital, Hong Kong SAR, Chinaen_US
dc.contributor.affiliationotherDivision of Gastroenterology and Hepatology, Prince of Wales Hospital, Hong Kong SAR, Chinaen_US
dc.identifier.pmid10706570en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34778/1/510310330_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/hep.510310330en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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