pubmed-article:16455894 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0220847 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0019682 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0019163 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0035668 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0021747 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0035525 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0444669 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0430420 | lld:lifeskim |
pubmed-article:16455894 | lifeskim:mentions | umls-concept:C0332293 | lld:lifeskim |
pubmed-article:16455894 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:16455894 | pubmed:dateCreated | 2006-2-3 | lld:pubmed |
pubmed-article:16455894 | pubmed:abstractText | Trak-C (Ortho-Clinical Diagnostics) is an enzyme-linked immunosorbent assay-based method capable of quantifying hepatitis C virus (HCV) core antigen (CA) in serum and could be an alternative to molecular detection and quantification of HCV RNA. We have evaluated the Trak-C assay in comparison with an HCV RNA quantitative assay (Versant HCV v3.0; Bayer Diagnostics) in the follow-up of 348 treated, human immunodeficiency virus (HIV)/HCV-coinfected patients included in the ANRS HC02 RIBAVIC trial. ANRS HC02 RIBAVIC is a therapeutic, multicenter, randomized protocol comparing the efficacy of alpha interferon 2b (IFN-alpha2b) (3 million units three times a week)-ribavirin (800 mg/day) to that of pegylated IFN-alpha2b (1.5 mug/kg of body weight/week)-ribavirin (800 mg/day) during 48 weeks of treatment of HIV/HCV-coinfected patients naïve to HCV treatment. Patients were assessed for virological analysis at day 0 and weeks 4, 12, 24, 48, and 72. Correlation of HCV RNA and HCV CA at the initiation of treatment was excellent (r = 0.92). HCV RNA and CA kinetics were similar during follow-up of HCV treatment from day 0 to week 72 whatever the group of response and genotype. The positive and negative predictive values of response to the treatment at week 4 were 59 and 94%, respectively, for HCV RNA load reduction of >2 log and 54 and 94%, respectively, for HCV CA below the threshold value (4.18 log(10) pg/ml . 10(4)). Trak-C, a new assay able to quantify CA in HIV/HCV-coinfected patients, correlates well with quantitative HCV RNA assays and is cheaper and easier to perform than molecular technology. HCV CA could be a valuable alternative test for therapeutic follow-up of coinfected patients treated with IFN plus ribavirin in developing countries. | lld:pubmed |
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pubmed-article:16455894 | pubmed:language | eng | lld:pubmed |
pubmed-article:16455894 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16455894 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16455894 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16455894 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16455894 | pubmed:month | Feb | lld:pubmed |
pubmed-article:16455894 | pubmed:issn | 0095-1137 | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:MorandPP | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:WuP PPP | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:LunelFF | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:CacoubPP | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:PerronneCC | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:CarratFF | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:PayanCC | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:PivertAA | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:Fafi-KremerSS | lld:pubmed |
pubmed-article:16455894 | pubmed:author | pubmed-author:DeshayesJJ | lld:pubmed |
pubmed-article:16455894 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16455894 | pubmed:volume | 44 | lld:pubmed |
pubmed-article:16455894 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16455894 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16455894 | pubmed:pagination | 417-22 | lld:pubmed |
pubmed-article:16455894 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:16455894 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16455894 | pubmed:articleTitle | Comparison of serum hepatitis C virus (HCV) RNA and core antigen levels in patients coinfected with human immunodeficiency virus and HCV and treated with interferon plus ribavirin. | lld:pubmed |
pubmed-article:16455894 | pubmed:affiliation | Laboratoire de Bactériologie-Virologie-Hygiène Hospitalière, CHU Angers, 4 rue Larrey, 49933 ANGERS Cedex, France. | lld:pubmed |
pubmed-article:16455894 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16455894 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:16455894 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:16455894 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:16455894 | pubmed:publicationType | Multicenter Study | lld:pubmed |