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- Publisher Website: 10.1111/j.1572-0241.2005.41530.x
- Scopus: eid_2-s2.0-19144371967
- PMID: 15842584
- WOS: WOS:000228489900017
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Article: Effect of lamivudine therapy on the serum covalently closed-circular (ccc) DNA of chronic hepatitis B infection
Title | Effect of lamivudine therapy on the serum covalently closed-circular (ccc) DNA of chronic hepatitis B infection |
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Authors | |
Issue Date | 2005 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ajg/index.html |
Citation | American Journal Of Gastroenterology, 2005, v. 100 n. 5, p. 1099-1103 How to Cite? |
Abstract | OBJECTIVE: To determine the effect of 1-yr lamivudine treatment on serum covalently closed-circular DNA (cccDNA) level. PATIENTS AND METHOD: Serum total HBV DNA and cccDNA levels at baseline, week 24, and week 52 were measured in 82 lamivudine-treated patients, 17 of whom received 1-yr placebo and acted as controls. RESULTS: There was a significant reduction in the cccDNA levels from baseline (median 3.0 × 106 copies/ml) to week 24 (33,476 copies/ml) and week 52 (48,694 copies/ml) (p < 0.001 for both). The median reduction in cccDNA level at week 24 and 52 were 2.21 and 2.12 logs, respectively, which were significantly greater than those of controls (0.31 log, p < 0.001; 0.2 log, p < 0.001, respectively). Fifteen patients (18.3%) developed YMDD mutations by week 52. Compared to patients without YMDD mutations, patients with YMDD mutations had significantly less median reduction of total HBV DNA level (4.44 vs 3.65 logs, respectively, p = 0.02) and cccDNA level (2.27 vs 1.65 logs, respectively, p = 0.016) at week 24 and significantly less median reduction of cccDNA at week 52 (2.35 vs 0.8 logs respectively, p < 0.001). CONCLUSIONS: One-year lamivudine treatment decreased serum cccDNA level by 2 logs. The chance of YMDD mutations at week 52 was related to the magnitude of viral suppression at week 24. © 2005 by Am. Coll. of Gastroenterology Published by Blackwell Publishing. |
Persistent Identifier | http://hdl.handle.net/10722/77043 |
ISSN | 2023 Impact Factor: 8.0 2023 SCImago Journal Rankings: 2.391 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Yuen, MF | en_HK |
dc.contributor.author | Wong, DKH | en_HK |
dc.contributor.author | Sum, SSM | en_HK |
dc.contributor.author | Yuan, HJ | en_HK |
dc.contributor.author | Yuen, JCH | 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 | 2010-09-06T07:27:39Z | - |
dc.date.available | 2010-09-06T07:27:39Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | American Journal Of Gastroenterology, 2005, v. 100 n. 5, p. 1099-1103 | en_HK |
dc.identifier.issn | 0002-9270 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77043 | - |
dc.description.abstract | OBJECTIVE: To determine the effect of 1-yr lamivudine treatment on serum covalently closed-circular DNA (cccDNA) level. PATIENTS AND METHOD: Serum total HBV DNA and cccDNA levels at baseline, week 24, and week 52 were measured in 82 lamivudine-treated patients, 17 of whom received 1-yr placebo and acted as controls. RESULTS: There was a significant reduction in the cccDNA levels from baseline (median 3.0 × 106 copies/ml) to week 24 (33,476 copies/ml) and week 52 (48,694 copies/ml) (p < 0.001 for both). The median reduction in cccDNA level at week 24 and 52 were 2.21 and 2.12 logs, respectively, which were significantly greater than those of controls (0.31 log, p < 0.001; 0.2 log, p < 0.001, respectively). Fifteen patients (18.3%) developed YMDD mutations by week 52. Compared to patients without YMDD mutations, patients with YMDD mutations had significantly less median reduction of total HBV DNA level (4.44 vs 3.65 logs, respectively, p = 0.02) and cccDNA level (2.27 vs 1.65 logs, respectively, p = 0.016) at week 24 and significantly less median reduction of cccDNA at week 52 (2.35 vs 0.8 logs respectively, p < 0.001). CONCLUSIONS: One-year lamivudine treatment decreased serum cccDNA level by 2 logs. The chance of YMDD mutations at week 52 was related to the magnitude of viral suppression at week 24. © 2005 by Am. Coll. of Gastroenterology Published by Blackwell Publishing. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ajg/index.html | en_HK |
dc.relation.ispartof | American Journal of Gastroenterology | en_HK |
dc.subject.mesh | Adolescent | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Amino Acid Motifs - drug effects - genetics | en_HK |
dc.subject.mesh | Anti-HIV Agents - therapeutic use | en_HK |
dc.subject.mesh | Aspartic Acid - drug effects - genetics | en_HK |
dc.subject.mesh | DNA, Circular - blood - drug effects | en_HK |
dc.subject.mesh | DNA, Viral - blood - drug effects | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Follow-Up Studies | en_HK |
dc.subject.mesh | Hepatitis B virus - drug effects - genetics | en_HK |
dc.subject.mesh | Hepatitis B, Chronic - drug therapy | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Isoleucine - genetics | en_HK |
dc.subject.mesh | Lamivudine - therapeutic use | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Methionine - drug effects - genetics | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Mutation - genetics | en_HK |
dc.subject.mesh | Placebos | en_HK |
dc.subject.mesh | Reverse Transcriptase Inhibitors - therapeutic use | en_HK |
dc.subject.mesh | Tyrosine - drug effects - genetics | en_HK |
dc.subject.mesh | Valine - genetics | en_HK |
dc.subject.mesh | Viral Load | en_HK |
dc.title | Effect of lamivudine therapy on the serum covalently closed-circular (ccc) DNA of chronic hepatitis B infection | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0002-9270&volume=100&issue=5&spage=1099&epage=103&date=2005&atitle=Effect+of+lamivudine+therapy+on+the+serum+covalently+closed-circular+(ccc)+DNA+of+chronic+hepatitis+B+infection. | 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_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1572-0241.2005.41530.x | en_HK |
dc.identifier.pmid | 15842584 | - |
dc.identifier.scopus | eid_2-s2.0-19144371967 | en_HK |
dc.identifier.hkuros | 101359 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-19144371967&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 100 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 1099 | en_HK |
dc.identifier.epage | 1103 | en_HK |
dc.identifier.isi | WOS:000228489900017 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=7401535819 | en_HK |
dc.identifier.scopusauthorid | Sum, SSM=6603889128 | en_HK |
dc.identifier.scopusauthorid | Yuan, HJ=7402446707 | en_HK |
dc.identifier.scopusauthorid | Yuen, JCH=7102620480 | 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 | 0002-9270 | - |