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- Publisher Website: 10.1111/j.1365-2036.2005.02410.x
- Scopus: eid_2-s2.0-16444362115
- PMID: 15801919
- WOS: WOS:000227901200006
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Article: Liver histology of Asian patients with chronic hepatitis B on prolonged lamivudine therapy
Title | Liver histology of Asian patients with chronic hepatitis B on prolonged lamivudine therapy |
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Authors | |
Issue Date | 2005 |
Publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/APT |
Citation | Alimentary Pharmacology And Therapeutics, 2005, v. 21 n. 7, p. 841-849 How to Cite? |
Abstract | Background: Long-term effect of YMDD mutations on liver histology in Chinese hepatitis B patients is unknown. Aim: To examine the effect of prolonged lamivudine treatment on liver histology in Chinese patients with and without YMDD mutations. Methods: Liver histology was assessed in 85 patients on long-term lamivudine at baseline and year 1, and at year 3 for 25 patients. Results: Comparing patients with and without YMDD mutations at year 1, the former had higher baseline median necroinflammatory (11 vs. six respectively, P = 0.014) and fibrosis scores (three vs. one respectively, P = 0.001). The proportion of patients with improvement in necroinflammation and worsening of fibrosis was comparable for patients with and without YMDD mutations at year 1 (57.1%, 14.3% vs. 55%, 15% respectively) and year 3 (57.9%, 26.3% vs. 50%, 16.7% respectively). Comparing the histology at year 1 and 3, more patients with YMDD mutations developing after year 1 had worsening of necroinflammation than patients with persistent YMDD wild type (53.8% vs. 25% respectively). Conclusions: Patients who developed YMDD mutations had higher baseline histological scores. With YMDD mutations, the liver histology became less favourable after 3 years than at the first year, although there was still improvement when compared with that at baseline. © 2005 Blackwell Publishing Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/76463 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 2.794 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Yuen, MF | en_HK |
dc.contributor.author | Chow, DHF | en_HK |
dc.contributor.author | Tsui, K | en_HK |
dc.contributor.author | Wong, BCY | en_HK |
dc.contributor.author | Yuen, JCH | en_HK |
dc.contributor.author | Wong, DKH | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.date.accessioned | 2010-09-06T07:21:30Z | - |
dc.date.available | 2010-09-06T07:21:30Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Alimentary Pharmacology And Therapeutics, 2005, v. 21 n. 7, p. 841-849 | en_HK |
dc.identifier.issn | 0269-2813 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/76463 | - |
dc.description.abstract | Background: Long-term effect of YMDD mutations on liver histology in Chinese hepatitis B patients is unknown. Aim: To examine the effect of prolonged lamivudine treatment on liver histology in Chinese patients with and without YMDD mutations. Methods: Liver histology was assessed in 85 patients on long-term lamivudine at baseline and year 1, and at year 3 for 25 patients. Results: Comparing patients with and without YMDD mutations at year 1, the former had higher baseline median necroinflammatory (11 vs. six respectively, P = 0.014) and fibrosis scores (three vs. one respectively, P = 0.001). The proportion of patients with improvement in necroinflammation and worsening of fibrosis was comparable for patients with and without YMDD mutations at year 1 (57.1%, 14.3% vs. 55%, 15% respectively) and year 3 (57.9%, 26.3% vs. 50%, 16.7% respectively). Comparing the histology at year 1 and 3, more patients with YMDD mutations developing after year 1 had worsening of necroinflammation than patients with persistent YMDD wild type (53.8% vs. 25% respectively). Conclusions: Patients who developed YMDD mutations had higher baseline histological scores. With YMDD mutations, the liver histology became less favourable after 3 years than at the first year, although there was still improvement when compared with that at baseline. © 2005 Blackwell Publishing Ltd. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/APT | en_HK |
dc.relation.ispartof | Alimentary Pharmacology and Therapeutics | en_HK |
dc.rights | Alimentary Pharmacology and Therapeutics. Copyright © Blackwell Publishing Ltd. | en_HK |
dc.subject.mesh | Adolescent | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Asian Continental Ancestry Group - genetics | en_HK |
dc.subject.mesh | Biopsy - methods | en_HK |
dc.subject.mesh | China - ethnology | en_HK |
dc.subject.mesh | DNA, Viral - genetics | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Hepatitis B virus - genetics | en_HK |
dc.subject.mesh | Hepatitis B, Chronic - drug therapy - ethnology - pathology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Lamivudine - therapeutic use | en_HK |
dc.subject.mesh | Liver - pathology | en_HK |
dc.subject.mesh | Liver Cirrhosis - pathology - virology | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Mutation - genetics | en_HK |
dc.subject.mesh | Reverse Transcriptase Inhibitors - therapeutic use | en_HK |
dc.title | Liver histology of Asian patients with chronic hepatitis B on prolonged lamivudine therapy | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0269-2813&volume=21&issue=7&spage=841&epage=9&date=2005&atitle=Liver+histology+of+Asian+patients+with+chronic+hepatitis+B+on+prolonged+lamivudine+therapy | en_HK |
dc.identifier.email | Yuen, MF:mfyuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, BCY:bcywong@hku.hk | en_HK |
dc.identifier.email | Wong, DKH:danywong@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, BCY=rp00429 | en_HK |
dc.identifier.authority | Wong, DKH=rp00492 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1365-2036.2005.02410.x | en_HK |
dc.identifier.pmid | 15801919 | - |
dc.identifier.scopus | eid_2-s2.0-16444362115 | en_HK |
dc.identifier.hkuros | 101363 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-16444362115&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 21 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 841 | en_HK |
dc.identifier.epage | 849 | en_HK |
dc.identifier.isi | WOS:000227901200006 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.scopusauthorid | Chow, DHF=35979710900 | en_HK |
dc.identifier.scopusauthorid | Tsui, K=8239092000 | en_HK |
dc.identifier.scopusauthorid | Wong, BCY=7402023340 | en_HK |
dc.identifier.scopusauthorid | Yuen, JCH=7102620480 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=7401535819 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.citeulike | 139408 | - |
dc.identifier.issnl | 0269-2813 | - |