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- Publisher Website: 10.1128/JCM.42.11.5036-5040.2004
- Scopus: eid_2-s2.0-8644265121
- PMID: 15528692
- WOS: WOS:000225149300019
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Article: Longitudinal study of hepatitis activity and viral replication before and after HBeAg seroconversion in chronic hepatitis B patients infected with genotypes B and C
Title | Longitudinal study of hepatitis activity and viral replication before and after HBeAg seroconversion in chronic hepatitis B patients infected with genotypes B and C |
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Authors | |
Issue Date | 2004 |
Publisher | American Society for Microbiology. |
Citation | Journal of Clinical Microbiology, 2004, v. 42 n. 11, p. 5036-5040 How to Cite? |
Abstract | The aims of this study were to compare chronic hepatitis B (CHB) patients with genotypes B and C for the probability of HBeAg seroconversion, hepatitis activity, and viral replication before and after HBeAg seroconversion and to compare the prevalence of core promoter and precore mutations. A total of 180 asymptomatic Chinese patients with CHB were monitored for a median of 53.8 months, and 38 patients with cirrhosis-related complications were studied. Hepatitis B virus (HBV) DNA levels were measured in 16 patients with HBeAg seroconversion at 3 months before, during, and 3 months after HBeAg seroconversion and in all patients at the last follow-up. Hepatitis B genotypes and core promoter and precore mutations were determined. Compared to patients with genotype C (n = 109), patients with subtype Ba (n = 69) had a higher rate of anti-HBe positivity on presentation (P = 0.05). HBeAg-positive patients with subtype Ba had a higher cumulative rate of HBeAg seroconversion than patients with genotype C (P = 0.02). However, there were no differences between the two groups with regard to the median HBV DNA levels before, during, and after HBeAg seroconversion; the probability of having persistently normal or elevated aminotransferase levels; and the median HBV DNA levels and liver biochemistry at the last follow-up. There was no difference in the prevalence of genotypes and core promoter and precore mutations between patients with and without cirrhosis-related complications. Though patients with subtype Ba had earlier HBeAg seroconversion, the liver biochemistry, HBV DNA levels in different phases of the disease, and the probability of development of cirrhosis-related complications were the same with genotypes Ba and C. |
Persistent Identifier | http://hdl.handle.net/10722/49037 |
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 1.653 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Yuen, MF | en_HK |
dc.contributor.author | Fung, SK | en_HK |
dc.contributor.author | Tanaka, Y | en_HK |
dc.contributor.author | Kato, T | en_HK |
dc.contributor.author | Mizokami, M | en_HK |
dc.contributor.author | Yuen, JCH | en_HK |
dc.contributor.author | Wong, DKH | en_HK |
dc.contributor.author | Yuan, HJ | en_HK |
dc.contributor.author | Sum, SM | en_HK |
dc.contributor.author | Chan, AOO | en_HK |
dc.contributor.author | Wong, BCY | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.date.accessioned | 2008-06-12T06:33:02Z | - |
dc.date.available | 2008-06-12T06:33:02Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Journal of Clinical Microbiology, 2004, v. 42 n. 11, p. 5036-5040 | en_HK |
dc.identifier.issn | 0095-1137 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/49037 | - |
dc.description.abstract | The aims of this study were to compare chronic hepatitis B (CHB) patients with genotypes B and C for the probability of HBeAg seroconversion, hepatitis activity, and viral replication before and after HBeAg seroconversion and to compare the prevalence of core promoter and precore mutations. A total of 180 asymptomatic Chinese patients with CHB were monitored for a median of 53.8 months, and 38 patients with cirrhosis-related complications were studied. Hepatitis B virus (HBV) DNA levels were measured in 16 patients with HBeAg seroconversion at 3 months before, during, and 3 months after HBeAg seroconversion and in all patients at the last follow-up. Hepatitis B genotypes and core promoter and precore mutations were determined. Compared to patients with genotype C (n = 109), patients with subtype Ba (n = 69) had a higher rate of anti-HBe positivity on presentation (P = 0.05). HBeAg-positive patients with subtype Ba had a higher cumulative rate of HBeAg seroconversion than patients with genotype C (P = 0.02). However, there were no differences between the two groups with regard to the median HBV DNA levels before, during, and after HBeAg seroconversion; the probability of having persistently normal or elevated aminotransferase levels; and the median HBV DNA levels and liver biochemistry at the last follow-up. There was no difference in the prevalence of genotypes and core promoter and precore mutations between patients with and without cirrhosis-related complications. Though patients with subtype Ba had earlier HBeAg seroconversion, the liver biochemistry, HBV DNA levels in different phases of the disease, and the probability of development of cirrhosis-related complications were the same with genotypes Ba and C. | en_HK |
dc.format.extent | 386 bytes | - |
dc.format.mimetype | text/html | - |
dc.language | eng | en_HK |
dc.publisher | American Society for Microbiology. | en_HK |
dc.relation.ispartof | Journal of Clinical Microbiology | en_HK |
dc.subject.mesh | Hepatitis B e Antigens - blood | en_HK |
dc.subject.mesh | Hepatitis B virus - classification - genetics - isolation & purification - pathogenicity | en_HK |
dc.subject.mesh | Hepatitis B, Chronic - physiopathology - virology | en_HK |
dc.subject.mesh | Liver Cirrhosis - physiopathology - virology | en_HK |
dc.subject.mesh | Virus Replication | en_HK |
dc.title | Longitudinal study of hepatitis activity and viral replication before and after HBeAg seroconversion in chronic hepatitis B patients infected with genotypes B and C | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Yuen, MF:mfyuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, DKH:danywong@hku.hk | en_HK |
dc.identifier.email | Wong, BCY:bcywong@hku.hk | en_HK |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_HK |
dc.identifier.authority | Yuen, MF=rp00479 | en_HK |
dc.identifier.authority | Wong, DKH=rp00492 | en_HK |
dc.identifier.authority | Wong, BCY=rp00429 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_HK |
dc.identifier.doi | 10.1128/JCM.42.11.5036-5040.2004 | en_HK |
dc.identifier.pmid | 15528692 | - |
dc.identifier.pmcid | PMC525264 | en_HK |
dc.identifier.scopus | eid_2-s2.0-8644265121 | en_HK |
dc.identifier.hkuros | 101373 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-8644265121&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 42 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 5036 | en_HK |
dc.identifier.epage | 5040 | en_HK |
dc.identifier.isi | WOS:000225149300019 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.scopusauthorid | Fung, SK=7201970083 | en_HK |
dc.identifier.scopusauthorid | Tanaka, Y=7405315865 | en_HK |
dc.identifier.scopusauthorid | Kato, T=7405277868 | en_HK |
dc.identifier.scopusauthorid | Mizokami, M=7103318255 | en_HK |
dc.identifier.scopusauthorid | Yuen, JCH=7102620480 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=7401535819 | en_HK |
dc.identifier.scopusauthorid | Yuan, HJ=7402446707 | en_HK |
dc.identifier.scopusauthorid | Sum, SM=6603889132 | en_HK |
dc.identifier.scopusauthorid | Chan, AOO=7403167965 | en_HK |
dc.identifier.scopusauthorid | Wong, BCY=7402023340 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.issnl | 0095-1137 | - |