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Article: Association of hepatitis B virus pre-S deletions with the development of hepatocellular carcinoma in chronic hepatitis B
Title | Association of hepatitis B virus pre-S deletions with the development of hepatocellular carcinoma in chronic hepatitis B | ||||
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Authors | |||||
Issue Date | 2011 | ||||
Publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org | ||||
Citation | Journal Of Infectious Diseases, 2011, v. 203 n. 5, p. 646-654 How to Cite? | ||||
Abstract | Background. We aimed to determine whether hepatitis B virus (HBV) pre-S deletion was an independent factor for the development of hepatocellular carcinoma (HCC). Methods. Pre-S deletions were determined in HBV isolates from 115 chronic hepatitis B (CHB) patients with HCC. Sixty-nine patients were further matched with 69 CHB patients without HCC for age, sex, hepatitis B e antigen (HBeAg) status, and HBV genotype. Results. HBV pre-S deletions were clustered mainly in the 3′ end of pre-S1 and 5′ end of pre-S2 regions. Adjusted for confounding risk factors, patients with HCC had a higher prevalence of HBV with pre-S deletions than did patients withoutHCC (23 [33.3%] of 69 vs 11 [15.9%] of 69; P=.018; odds ratio [OR], 2.64). In particular, only pre-S2 deletions but not pre-S1 deletions were significantly associated with the development of HCC (P = .020). A higher prevalence of pre-S deletions was observed in HBV isolates from HCC patients under the age of 50 years than fromthose older than 50 years (10 [62.5%] of 16 vs 13 [24.5%] of 53; P = .012; OR, 5.13). Emergence of de novo pre-S deletions was documented before the development of HCC. Conclusions. HBV pre-S2 deletions were an independent factor associated with the development of HCC. Its oncogenic role may be more important in young patients with HCC. © The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/137388 | ||||
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 2.387 | ||||
PubMed Central ID | |||||
ISI Accession Number ID |
Funding Information: Hepatology Research Fund, Department of Medicine, The University of Hong Kong | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yeung, P | en_HK |
dc.contributor.author | Wong, DKH | 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 | 2011-08-26T14:24:14Z | - |
dc.date.available | 2011-08-26T14:24:14Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Journal Of Infectious Diseases, 2011, v. 203 n. 5, p. 646-654 | en_HK |
dc.identifier.issn | 0022-1899 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/137388 | - |
dc.description.abstract | Background. We aimed to determine whether hepatitis B virus (HBV) pre-S deletion was an independent factor for the development of hepatocellular carcinoma (HCC). Methods. Pre-S deletions were determined in HBV isolates from 115 chronic hepatitis B (CHB) patients with HCC. Sixty-nine patients were further matched with 69 CHB patients without HCC for age, sex, hepatitis B e antigen (HBeAg) status, and HBV genotype. Results. HBV pre-S deletions were clustered mainly in the 3′ end of pre-S1 and 5′ end of pre-S2 regions. Adjusted for confounding risk factors, patients with HCC had a higher prevalence of HBV with pre-S deletions than did patients withoutHCC (23 [33.3%] of 69 vs 11 [15.9%] of 69; P=.018; odds ratio [OR], 2.64). In particular, only pre-S2 deletions but not pre-S1 deletions were significantly associated with the development of HCC (P = .020). A higher prevalence of pre-S deletions was observed in HBV isolates from HCC patients under the age of 50 years than fromthose older than 50 years (10 [62.5%] of 16 vs 13 [24.5%] of 53; P = .012; OR, 5.13). Emergence of de novo pre-S deletions was documented before the development of HCC. Conclusions. HBV pre-S2 deletions were an independent factor associated with the development of HCC. Its oncogenic role may be more important in young patients with HCC. © The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org | en_HK |
dc.relation.ispartof | Journal of Infectious Diseases | en_HK |
dc.subject.mesh | Carcinoma, Hepatocellular - epidemiology - genetics - virology | en_US |
dc.subject.mesh | Gene Deletion | en_US |
dc.subject.mesh | Hepatitis B virus - chemistry - classification - genetics | en_US |
dc.subject.mesh | Hepatitis B, Chronic - complications - genetics - virology | en_US |
dc.subject.mesh | Liver Neoplasms - epidemiology - genetics - virology | en_US |
dc.title | Association of hepatitis B virus pre-S deletions with the development of hepatocellular carcinoma in chronic hepatitis B | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-1899&volume=203&issue=5&spage=646&epage=654&date=2011&atitle=Association+of+hepatitis+B+virus+pre-S+deletions+with+the+development+of+hepatocellular+carcinoma+in+chronic+hepatitis+B | en_US |
dc.identifier.email | Wong, DKH: 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, DKH=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_OA_fulltext | en_US |
dc.identifier.doi | 10.1093/infdis/jiq096 | en_HK |
dc.identifier.pmid | 21227916 | - |
dc.identifier.pmcid | PMC3072715 | en_US |
dc.identifier.scopus | eid_2-s2.0-79751523518 | en_HK |
dc.identifier.hkuros | 189867 | en_US |
dc.identifier.hkuros | 188146 | en_US |
dc.identifier.hkuros | 213685 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79751523518&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 203 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 646 | en_HK |
dc.identifier.epage | 654 | en_HK |
dc.identifier.isi | WOS:000287028000011 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yeung, P=35081534000 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=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 | 0022-1899 | - |