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Conference Paper: Hepatitis B Virus genotypes B and C do not affect the anti-viral response to Lamivudine
Title | Hepatitis B Virus genotypes B and C do not affect the anti-viral response to Lamivudine |
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Authors | |
Issue Date | 2003 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ |
Citation | The 55th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD 2003), Boston, MA., 25-29 November 2003. In Hepatology, 2003, v. 38 suppl. S4, p. 723A, abstract no. 1179 How to Cite? |
Abstract | BACKGROUND: To date, there have been no studies examining the role of hepatitis B virus (HBV) genotypes on the response to lamivudine therapy and the development of YMDD mutations. AIMS: The present study aimed at determining any differences in the anti-viral response and risk of YMDD mutations between lamivudine-treated patients with HBV genotype B and genotype C. PATIENTS AND METHODS: Eighty-two patients receiving lamivudine were recruited. HBV genotypes at baseline and YMDD mutations at week 52 were determined by line probe assays (LiPA). HBV DNA levels were determined by the Cobas Amplicor HBV Monitor Test. RESULTS: Seventeen (20.7%) and sixty-four (78%) patients had single genotypes of B and C respectively. At both week 24 and 52 there were no differences in the median reduction of HBV DNA levels (median 4 logs drop), the median reduction of alanine aminotransferase (ALT) levels, and the proportion with normalization of ALT [8/8 (100%) vs. 26/37 (70.3%), p=O.19] between patients with genotypes B and C. The rate of HBeAg seroconversion [3/17 (17.6%) vs. 6/64 (9.4%)' p=0.39] and the chance of YMDD mutation development [3/17 (17.6%) vs. 12/@ (18.8%), p=1.0] at week 52 were also similar between patients with genotype B and C respectively. CONCLUSIONS: There were no difference in the anti-viral response and the rate of development of YMDD mutations in Chinese patients with genotype B and C after one year of lamivudine. Determination of HBV genotypes before lamivudine therapy to predict treatment responsiveness is not necessary in Chinese patients. |
Description | This free journal suppl. entitled: AASLD Abstracts |
Persistent Identifier | http://hdl.handle.net/10722/101970 |
ISSN | 2023 Impact Factor: 12.9 2023 SCImago Journal Rankings: 5.011 |
DC Field | Value | Language |
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dc.contributor.author | Yuen, MF | - |
dc.contributor.author | Wong, DKH | - |
dc.contributor.author | Sablon, E | - |
dc.contributor.author | Yuan, H | - |
dc.contributor.author | Sum, SM | - |
dc.contributor.author | Hui, CK | - |
dc.contributor.author | Wong, BCY | - |
dc.contributor.author | Lai, CL | - |
dc.date.accessioned | 2010-09-25T20:11:50Z | - |
dc.date.available | 2010-09-25T20:11:50Z | - |
dc.date.issued | 2003 | - |
dc.identifier.citation | The 55th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD 2003), Boston, MA., 25-29 November 2003. In Hepatology, 2003, v. 38 suppl. S4, p. 723A, abstract no. 1179 | - |
dc.identifier.issn | 0270-9139 | - |
dc.identifier.uri | http://hdl.handle.net/10722/101970 | - |
dc.description | This free journal suppl. entitled: AASLD Abstracts | - |
dc.description.abstract | BACKGROUND: To date, there have been no studies examining the role of hepatitis B virus (HBV) genotypes on the response to lamivudine therapy and the development of YMDD mutations. AIMS: The present study aimed at determining any differences in the anti-viral response and risk of YMDD mutations between lamivudine-treated patients with HBV genotype B and genotype C. PATIENTS AND METHODS: Eighty-two patients receiving lamivudine were recruited. HBV genotypes at baseline and YMDD mutations at week 52 were determined by line probe assays (LiPA). HBV DNA levels were determined by the Cobas Amplicor HBV Monitor Test. RESULTS: Seventeen (20.7%) and sixty-four (78%) patients had single genotypes of B and C respectively. At both week 24 and 52 there were no differences in the median reduction of HBV DNA levels (median 4 logs drop), the median reduction of alanine aminotransferase (ALT) levels, and the proportion with normalization of ALT [8/8 (100%) vs. 26/37 (70.3%), p=O.19] between patients with genotypes B and C. The rate of HBeAg seroconversion [3/17 (17.6%) vs. 6/64 (9.4%)' p=0.39] and the chance of YMDD mutation development [3/17 (17.6%) vs. 12/@ (18.8%), p=1.0] at week 52 were also similar between patients with genotype B and C respectively. CONCLUSIONS: There were no difference in the anti-viral response and the rate of development of YMDD mutations in Chinese patients with genotype B and C after one year of lamivudine. Determination of HBV genotypes before lamivudine therapy to predict treatment responsiveness is not necessary in Chinese patients. | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ | - |
dc.relation.ispartof | Hepatology | - |
dc.rights | Hepatology. Copyright © John Wiley & Sons, Inc. | - |
dc.title | Hepatitis B Virus genotypes B and C do not affect the anti-viral response to Lamivudine | - |
dc.type | Conference_Paper | - |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0270-9139&volume=&spage=A1179&epage=&date=2003&atitle=Hepatitis+B+virus+genotypes+B+and+C+do+not+affect+the+anti-viral+response+to+lamivudine | en_HK |
dc.identifier.email | Yuen, MF: mfyuen@hkucc.hku.hk | - |
dc.identifier.email | Wong, DKH: danwong@hku.hk | - |
dc.identifier.email | Wong, BCY: bcywong@hku.hk | - |
dc.identifier.email | Lai, CL: hrmelcl@hku.hk | - |
dc.identifier.authority | Yuen, MF=rp00479 | - |
dc.identifier.authority | Wong, DKH=rp00492 | - |
dc.identifier.authority | Wong, BCY=rp00429 | - |
dc.identifier.authority | Lai, CL=rp00314 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1002/hep.1840380509 | - |
dc.identifier.hkuros | 95947 | - |
dc.identifier.hkuros | 130914 | - |
dc.identifier.volume | 38 | - |
dc.identifier.issue | suppl. S4 | - |
dc.identifier.spage | 723A, abstract no. 1179 | - |
dc.identifier.epage | 723A, abstract no. 1179 | - |
dc.identifier.issnl | 0270-9139 | - |