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Article: A case-control study of response to lamivudine therapy for 2 years in Japanese and Chinese patients chronically infected with hepatitis B virus of genotypes Bj, Ba and C
Title | A case-control study of response to lamivudine therapy for 2 years in Japanese and Chinese patients chronically infected with hepatitis B virus of genotypes Bj, Ba and C |
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Authors | |
Keywords | HBV genotype Ba, Bj, C Lamivudine Resistant mutation Response to therapy |
Issue Date | 2006 |
Publisher | Blackwell Publishing Ltd. |
Citation | Hepatology Research, 2006, v. 35 n. 2, p. 127-134 How to Cite? |
Abstract | Background/aims: In eastern Asian countries, hepatitis B virus (HBV) genotype Ba (HBV/Ba), HBV/Bj and HBV/C are prevalent. The aim was to investigate the response or resistance to lamivudine therapy among patients with different HBV genotypes. Methods: Of 67 Japanese and Chinese patients with chronic hepatitis B, 18 patients with HBV/Bj, 15 with HBV/Ba and 34 with HBV/C were selected for a case-control study matched according to gender and age. All the patients were treated with lamivudine for 2 years and evaluated the response or emergence of the YMDD mutation at year 2 during the treatment. HBV genotypes were detected by the restriction fragment length polymorphism. The YMDD mutation was detected by the direct sequencing after amplification by PCR. Results: At year 2 during therapy, 44.8% of the patients showed normalization of ALT and undetectable HBV DNA (favorable response), 35.8% developed the YMDD mutation. There was no significant difference of response to the therapy among the three genotype groups. The emergence of the YMDD mutation was associated with HBV/C. By the multiple logistic regression analysis, however, the significant factor of a favorable response was a higher pretreatment ALT level and negative HBeAg status and the significant factor of the emergence of the YMDD mutation was HBV/C. Conclusions: Higher pretreatment ALT level, HBeAg status or HBV genotype may affect the response or resistance to lamivudine therapy. © 2006 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/77954 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.241 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Orito, E | en_HK |
dc.contributor.author | Fujiwara, K | en_HK |
dc.contributor.author | Tanaka, Y | en_HK |
dc.contributor.author | Yuen, MF | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.contributor.author | Kato, T | en_HK |
dc.contributor.author | Sugauchi, F | en_HK |
dc.contributor.author | Kusakabe, A | en_HK |
dc.contributor.author | Sata, M | en_HK |
dc.contributor.author | Okanoue, T | en_HK |
dc.contributor.author | Niitsuma, H | en_HK |
dc.contributor.author | Sakugawa, H | en_HK |
dc.contributor.author | Hasegawa, I | en_HK |
dc.contributor.author | Mizokami, M | en_HK |
dc.date.accessioned | 2010-09-06T07:37:34Z | - |
dc.date.available | 2010-09-06T07:37:34Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Hepatology Research, 2006, v. 35 n. 2, p. 127-134 | en_HK |
dc.identifier.issn | 1386-6346 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77954 | - |
dc.description.abstract | Background/aims: In eastern Asian countries, hepatitis B virus (HBV) genotype Ba (HBV/Ba), HBV/Bj and HBV/C are prevalent. The aim was to investigate the response or resistance to lamivudine therapy among patients with different HBV genotypes. Methods: Of 67 Japanese and Chinese patients with chronic hepatitis B, 18 patients with HBV/Bj, 15 with HBV/Ba and 34 with HBV/C were selected for a case-control study matched according to gender and age. All the patients were treated with lamivudine for 2 years and evaluated the response or emergence of the YMDD mutation at year 2 during the treatment. HBV genotypes were detected by the restriction fragment length polymorphism. The YMDD mutation was detected by the direct sequencing after amplification by PCR. Results: At year 2 during therapy, 44.8% of the patients showed normalization of ALT and undetectable HBV DNA (favorable response), 35.8% developed the YMDD mutation. There was no significant difference of response to the therapy among the three genotype groups. The emergence of the YMDD mutation was associated with HBV/C. By the multiple logistic regression analysis, however, the significant factor of a favorable response was a higher pretreatment ALT level and negative HBeAg status and the significant factor of the emergence of the YMDD mutation was HBV/C. Conclusions: Higher pretreatment ALT level, HBeAg status or HBV genotype may affect the response or resistance to lamivudine therapy. © 2006 Elsevier Ireland Ltd. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Ltd. | en_HK |
dc.relation.ispartof | Hepatology Research | en_HK |
dc.rights | Hepatology Research. Copyright © Blackwell Publishing Ltd. | en_HK |
dc.subject | HBV genotype Ba, Bj, C | en_HK |
dc.subject | Lamivudine | en_HK |
dc.subject | Resistant mutation | en_HK |
dc.subject | Response to therapy | en_HK |
dc.title | A case-control study of response to lamivudine therapy for 2 years in Japanese and Chinese patients chronically infected with hepatitis B virus of genotypes Bj, Ba and C | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1386-6346&volume=35&spage=127&epage=134&date=2006&atitle=A+case-control+study+of+response+to+lamivudine+therapy+for+2+years+in+Japanese+and+Chinese+patients+chronically+infected+with+hepatitis+B+virus+of+genotypes+Bj,+Ba+and+C | en_HK |
dc.identifier.email | Yuen, MF:mfyuen@hkucc.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 | Lai, CL=rp00314 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.hepres.2006.03.005 | en_HK |
dc.identifier.scopus | eid_2-s2.0-33646801638 | en_HK |
dc.identifier.hkuros | 121892 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33646801638&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 35 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 127 | en_HK |
dc.identifier.epage | 134 | en_HK |
dc.identifier.isi | WOS:000238585800009 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Orito, E=7006161634 | en_HK |
dc.identifier.scopusauthorid | Fujiwara, K=7403468620 | en_HK |
dc.identifier.scopusauthorid | Tanaka, Y=7405315865 | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.scopusauthorid | Kato, T=7405277868 | en_HK |
dc.identifier.scopusauthorid | Sugauchi, F=7004837927 | en_HK |
dc.identifier.scopusauthorid | Kusakabe, A=13608375400 | en_HK |
dc.identifier.scopusauthorid | Sata, M=35355942700 | en_HK |
dc.identifier.scopusauthorid | Okanoue, T=7101962104 | en_HK |
dc.identifier.scopusauthorid | Niitsuma, H=7006500814 | en_HK |
dc.identifier.scopusauthorid | Sakugawa, H=7006875192 | en_HK |
dc.identifier.scopusauthorid | Hasegawa, I=7101889902 | en_HK |
dc.identifier.scopusauthorid | Mizokami, M=7103318255 | en_HK |
dc.identifier.issnl | 1386-6346 | - |