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- Publisher Website: 10.1002/jmv.21901
- Scopus: eid_2-s2.0-79952197374
- PMID: 20872710
- WOS: WOS:000282266900006
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Article: Profile of pre-S deletions in the natural history of chronic hepatitis B infection.
Title | Profile of pre-S deletions in the natural history of chronic hepatitis B infection. |
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Authors | |
Keywords | Chronic hepatitis B Epidemiology Genotype HBeAg seroconversion Pre-S deletions |
Issue Date | 2010 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/32763 |
Citation | Journal Of Medical Virology, 2010, v. 82 n. 11, p. 1843-1849 How to Cite? |
Abstract | It have been suggested that hepatitis B virus (HBV) pre-S deletions may play a role in hepatocarcinogenesis. The aim of the study was to determine the prevalence of pre-S deletions in chronic hepatitis B patients in Hong Kong, the factors associated with the deletions and its relationship with hepatitis B e antigen (HBeAg) seroconversion. HBV pre-S deletions were determined by nucleotide sequence analysis in 178 patients with chronic HBV (cross-sectional study). Eighty-four patients had paired samples before and after HBeAg seroconversion (longitudinal study). The prevalence of pre-S deletions was 12.9% (23/178). A majority of the pre-S deletions (73.9%) occurred in the 5' terminus of pre-S2 region whereas deletions in the pre-S1 region appeared less frequently (47.8%). There was no relationship between age and pre-S deletions. Male gender [odds ratio (OR)=10.88; 95% confidence interval (CI)=1.37-86.52; P=0.024] and HBV genotype C (OR=13.85; 95% CI=3.05-62.92; P=0.001) were independent factors associated with pre-S deletions. Only 17 out of the 84 patients with paired samples before and after HBeAg seroconversion had pre-S deletions. The patterns of pre-S deletions before and after HBeAg seroconversion were variable. Compared with genotype B, HBV genotype C was associated with earlier emergence of pre-S deletions. In conclusion, 12.9% of chronic HBV carriers had pre-S deletions (predominantly pre-S2 deletions) in a geographical area highly endemic for chronic hepatitis B. Male gender and HBV genotype C were associated independently with the development of pre-S deletion mutations. There was no clear relationship between HBeAg seroconversion and pre-S deletions. © 2010 Wiley-Liss, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/135240 |
ISSN | 2023 Impact Factor: 6.8 2023 SCImago Journal Rankings: 1.560 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Yeung, P | en_HK |
dc.contributor.author | Wong, DK | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.contributor.author | Fung, J | en_HK |
dc.contributor.author | Seto, WK | en_HK |
dc.contributor.author | Yuen, MF | en_HK |
dc.date.accessioned | 2011-07-27T01:30:28Z | - |
dc.date.available | 2011-07-27T01:30:28Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Journal Of Medical Virology, 2010, v. 82 n. 11, p. 1843-1849 | en_HK |
dc.identifier.issn | 1096-9071 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/135240 | - |
dc.description.abstract | It have been suggested that hepatitis B virus (HBV) pre-S deletions may play a role in hepatocarcinogenesis. The aim of the study was to determine the prevalence of pre-S deletions in chronic hepatitis B patients in Hong Kong, the factors associated with the deletions and its relationship with hepatitis B e antigen (HBeAg) seroconversion. HBV pre-S deletions were determined by nucleotide sequence analysis in 178 patients with chronic HBV (cross-sectional study). Eighty-four patients had paired samples before and after HBeAg seroconversion (longitudinal study). The prevalence of pre-S deletions was 12.9% (23/178). A majority of the pre-S deletions (73.9%) occurred in the 5' terminus of pre-S2 region whereas deletions in the pre-S1 region appeared less frequently (47.8%). There was no relationship between age and pre-S deletions. Male gender [odds ratio (OR)=10.88; 95% confidence interval (CI)=1.37-86.52; P=0.024] and HBV genotype C (OR=13.85; 95% CI=3.05-62.92; P=0.001) were independent factors associated with pre-S deletions. Only 17 out of the 84 patients with paired samples before and after HBeAg seroconversion had pre-S deletions. The patterns of pre-S deletions before and after HBeAg seroconversion were variable. Compared with genotype B, HBV genotype C was associated with earlier emergence of pre-S deletions. In conclusion, 12.9% of chronic HBV carriers had pre-S deletions (predominantly pre-S2 deletions) in a geographical area highly endemic for chronic hepatitis B. Male gender and HBV genotype C were associated independently with the development of pre-S deletion mutations. There was no clear relationship between HBeAg seroconversion and pre-S deletions. © 2010 Wiley-Liss, Inc. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/32763 | - |
dc.relation.ispartof | Journal of medical virology | en_HK |
dc.rights | Journal of Medical Virology. Copyright © John Wiley & Sons, Inc. | - |
dc.subject | Chronic hepatitis B | - |
dc.subject | Epidemiology | - |
dc.subject | Genotype | - |
dc.subject | HBeAg seroconversion | - |
dc.subject | Pre-S deletions | - |
dc.subject.mesh | Disease Progression | - |
dc.subject.mesh | Hepatitis B Surface Antigens - genetics | - |
dc.subject.mesh | Hepatitis B virus - classification - genetics | - |
dc.subject.mesh | Hepatitis B, Chronic - epidemiology - physiopathology - virology | - |
dc.subject.mesh | Protein Precursors - genetics | - |
dc.title | Profile of pre-S deletions in the natural history of chronic hepatitis B infection. | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Wong, DK: danywong@hku.hk | en_HK |
dc.identifier.email | Lai, CL: hrmelcl@hku.hk | en_HK |
dc.identifier.email | Fung, J: jfung@sicklehut.com | en_HK |
dc.identifier.email | Seto, WK: wkseto2@hku.hk | en_HK |
dc.identifier.email | Yuen, MF: mfyuen@hku.hk | en_HK |
dc.identifier.authority | Wong, DK=rp00492 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.identifier.authority | Fung, J=rp00518 | en_HK |
dc.identifier.authority | Seto, WK=rp01659 | en_HK |
dc.identifier.authority | Yuen, MF=rp00479 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/jmv.21901 | - |
dc.identifier.pmid | 20872710 | en_HK |
dc.identifier.scopus | eid_2-s2.0-79952197374 | en_HK |
dc.identifier.hkuros | 188143 | en_US |
dc.identifier.hkuros | 189967 | - |
dc.identifier.hkuros | 213671 | - |
dc.identifier.volume | 82 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 1843 | en_HK |
dc.identifier.epage | 1849 | en_HK |
dc.identifier.isi | WOS:000282266900006 | - |
dc.publisher.place | United States | - |
dc.identifier.scopusauthorid | Yeung, P=35081534000 | en_HK |
dc.identifier.scopusauthorid | Wong, DK=7401535819 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.scopusauthorid | Fung, J=23091109300 | en_HK |
dc.identifier.scopusauthorid | Seto, WK=23390675900 | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.issnl | 0146-6615 | - |