File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1086/591252
- Scopus: eid_2-s2.0-51749084677
- PMID: 18657036
- WOS: WOS:000258661500003
- Find via
Supplementary
-
Bookmarks:
- CiteULike: 1
- Citations:
- Appears in Collections:
Article: Chronic hepatitis C virus genotype 6 infection: Response to pegylated interferon and ribavirin
Title | Chronic hepatitis C virus genotype 6 infection: Response to pegylated interferon and ribavirin |
---|---|
Authors | |
Issue Date | 2008 |
Publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org |
Citation | Journal Of Infectious Diseases, 2008, v. 198 n. 6, p. 808-812 How to Cite? |
Abstract | Background. To date, no study has evaluated pegylated interferon for the treatment of chronic infection with hepatitis C virus (HCV) genotype 6. We aimed to determine the efficacy of pegylated interferon plus ribavirin for treating infection with genotype 6 versus genotype 1. Methods. Forty-two patients chronically infected with HCV (for genotype 1, n = 21; for genotype 6, n = 21) were treated with pegylated interferon α-2a (n = 20) or α-2b (n = 22) combined with oral ribavirin for 48 weeks. Results. There was no difference between genotypes 1 and 6 in the rates of early virological response (76% vs. 81%; P > .05) and end-of-treatment response (71% vs. 81%; P > .05). Patients infected with genotype 6 had a higher rate of sustained virological response (SVR) than did patients infected with genotype 1 (86% vs. 52%; P = .019). The overall adverse-effects profile was similar in both genotype groups. There was no significant difference in the rate of SVR between patients receiving pegylated interferon α-2a and those receiving α-2b. Multivariate analysis showed that genotype was the only significant factor associated with SVR (P = .039). Conclusions. Treatment with pegylated interferon and ribavirin for 48 weeks resulted in a significantly higher rate of SVR in patients infected with genotype 6 than in those infected with genotype 1. Further studies are required to determine whether lower dosages and 24 weeks of therapy may be sufficient for the treatment of genotype 6 infection. © 2008 by the Infectious Diseases Society of America. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/59291 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 2.387 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Fung, J | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.contributor.author | Hung, I | en_HK |
dc.contributor.author | Young, J | en_HK |
dc.contributor.author | Cheng, C | en_HK |
dc.contributor.author | Wong, D | en_HK |
dc.contributor.author | Yuen, MF | en_HK |
dc.date.accessioned | 2010-05-31T03:47:07Z | - |
dc.date.available | 2010-05-31T03:47:07Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Journal Of Infectious Diseases, 2008, v. 198 n. 6, p. 808-812 | en_HK |
dc.identifier.issn | 0022-1899 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/59291 | - |
dc.description.abstract | Background. To date, no study has evaluated pegylated interferon for the treatment of chronic infection with hepatitis C virus (HCV) genotype 6. We aimed to determine the efficacy of pegylated interferon plus ribavirin for treating infection with genotype 6 versus genotype 1. Methods. Forty-two patients chronically infected with HCV (for genotype 1, n = 21; for genotype 6, n = 21) were treated with pegylated interferon α-2a (n = 20) or α-2b (n = 22) combined with oral ribavirin for 48 weeks. Results. There was no difference between genotypes 1 and 6 in the rates of early virological response (76% vs. 81%; P > .05) and end-of-treatment response (71% vs. 81%; P > .05). Patients infected with genotype 6 had a higher rate of sustained virological response (SVR) than did patients infected with genotype 1 (86% vs. 52%; P = .019). The overall adverse-effects profile was similar in both genotype groups. There was no significant difference in the rate of SVR between patients receiving pegylated interferon α-2a and those receiving α-2b. Multivariate analysis showed that genotype was the only significant factor associated with SVR (P = .039). Conclusions. Treatment with pegylated interferon and ribavirin for 48 weeks resulted in a significantly higher rate of SVR in patients infected with genotype 6 than in those infected with genotype 1. Further studies are required to determine whether lower dosages and 24 weeks of therapy may be sufficient for the treatment of genotype 6 infection. © 2008 by the Infectious Diseases Society of America. All rights reserved. | en_HK |
dc.language | eng | en_HK |
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.rights | Journal of Infectious Diseases. Copyright © University of Chicago Press. | en_HK |
dc.subject.mesh | Antiviral Agents - therapeutic use | en_HK |
dc.subject.mesh | Drug Therapy, Combination | en_HK |
dc.subject.mesh | Genotype | en_HK |
dc.subject.mesh | Hepacivirus - genetics | en_HK |
dc.subject.mesh | Hepatitis C, Chronic - drug therapy - virology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Interferon-alpha - therapeutic use | en_HK |
dc.subject.mesh | Polyethylene Glycols - therapeutic use | en_HK |
dc.subject.mesh | Recombinant Proteins | en_HK |
dc.subject.mesh | Ribavirin - therapeutic use | en_HK |
dc.title | Chronic hepatitis C virus genotype 6 infection: Response to pegylated interferon and ribavirin | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-1899&volume=198&issue=6&spage=808&epage=12&date=2008&atitle=Chronic+hepatitis+C+virus+genotype+6+infection:+response+to+pegylated+interferon+and+ribavirin | en_HK |
dc.identifier.email | Fung, J:jfung@sicklehut.com | en_HK |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_HK |
dc.identifier.email | Hung, I:ivanhung@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, D:danywong@hku.hk | en_HK |
dc.identifier.email | Yuen, MF:mfyuen@hkucc.hku.hk | en_HK |
dc.identifier.authority | Fung, J=rp00518 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.identifier.authority | Hung, I=rp00508 | en_HK |
dc.identifier.authority | Wong, D=rp00492 | en_HK |
dc.identifier.authority | Yuen, MF=rp00479 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1086/591252 | en_HK |
dc.identifier.pmid | 18657036 | - |
dc.identifier.scopus | eid_2-s2.0-51749084677 | en_HK |
dc.identifier.hkuros | 149253 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-51749084677&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 198 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 808 | en_HK |
dc.identifier.epage | 812 | en_HK |
dc.identifier.isi | WOS:000258661500003 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Fung, J=23091109300 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.scopusauthorid | Hung, I=7006103457 | en_HK |
dc.identifier.scopusauthorid | Young, J=16949957200 | en_HK |
dc.identifier.scopusauthorid | Cheng, C=24802108600 | en_HK |
dc.identifier.scopusauthorid | Wong, D=7401535819 | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.citeulike | 3083252 | - |
dc.identifier.issnl | 0022-1899 | - |