Source:http://linkedlifedata.com/resource/pubmed/id/15451178
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2004-9-28
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pubmed:abstractText |
The clinical significance of coinfection of SENV-H among patients with chronic hepatitis C (CHC) and the response to combination therapy with high-dose interferon-alpha (IFN) plus ribavirin in Taiwan are uncertain. A total of 151 (120 histologically proved) naïve CHC patients who received 6 MU IFN thrice a week plus ribavirin for 24 weeks therapy were enrolled in this study. SENV-H DNA was tested by PCR method. Of 151 patients, 29 (19.2%) were positive for SENV-H DNA. The positive SENV-H DNA was significantly associated with HCV genotype 1b than non-1b infection (69.0% versus 43.4%; P = 0.011). No other clinical, histopathological and virological factor was related to positive SENV-H DNA. After combination therapy, the rate of sustained viral response (SVR) of HCV and SENV-H were 66.9 and 78.3%, respectively. By multivariate analyses, the significant factors associated with HCV SVR after combination therapy were HCV genotype non-1b, pretreatment HCV RNA levels less than 200,000 IU/mL, and younger age. We conclude that coexistent SENV-H infection, apparently associated with HCV genotype 1b, is found among 19.2% of Taiwanese CHC patients. Both HCV and SENV-H are highly susceptible to combination therapy with high dose IFN and ribavirin and SENV-H coinfection does not affect the HCV response.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antiviral Agents,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon Type I,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Ribavirin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0166-3542
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
64
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
47-53
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:15451178-Adult,
pubmed-meshheading:15451178-Aged,
pubmed-meshheading:15451178-Antiviral Agents,
pubmed-meshheading:15451178-Base Sequence,
pubmed-meshheading:15451178-Circoviridae,
pubmed-meshheading:15451178-Circoviridae Infections,
pubmed-meshheading:15451178-DNA, Viral,
pubmed-meshheading:15451178-Female,
pubmed-meshheading:15451178-Hepatitis C, Chronic,
pubmed-meshheading:15451178-Humans,
pubmed-meshheading:15451178-Interferon Type I,
pubmed-meshheading:15451178-Male,
pubmed-meshheading:15451178-Middle Aged,
pubmed-meshheading:15451178-Recombinant Proteins,
pubmed-meshheading:15451178-Ribavirin,
pubmed-meshheading:15451178-Taiwan,
pubmed-meshheading:15451178-Viremia
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pubmed:year |
2004
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pubmed:articleTitle |
The prevalence and clinical characteristics of coinfection of SENV-H among Taiwanese chronic hepatitis C patients with combination therapy of high-dose interferon-alfa and ribavirin.
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pubmed:affiliation |
Department of Internal Medicine, Hepatobiliary Division, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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