| Literature DB >> 18929599 |
Jonathan Pol1, Catherine Le Pendeven, Agnes Beby-Defaux, Elodie Rabut, Jean Philippe Jais, Marilyse Pilloux, Catherine Osada, Fadila Zatla, Hichem Assami, Jean Didier Grange, Dina Kremsdorf, Jean Claude Nicolas, Patrick Soussan.
Abstract
The quantitation of human hepatitis B virus (HBV) in the serum of infected patients is recommended to characterize the course of chronic HBV infection. The aim of this prospective study was to evaluate the performance of the Abbott RealTime PCR assay for HBV DNA quantitation by comparison with the standard Versant HBV DNA 3.0 assay. The better sensitivity and broader dynamic range of HBV DNA quantitation using the Abbott RealTime PCR assay was confirmed by the study of 362 serum samples from 311 patients. In addition, data analysis revealed the concordance of HBV DNA quantitations between the two assays. When this evaluation was assessed as a function of HBV genotype, there was discordance for HBV genotype C samples. Thus, we performed an in-house PCR to confirm the discrepancy observed regarding the HBV genotypes. The in-house PCR results agreed better with the Abbott RealTime PCR method when compared with the standard hybridization assay. In conclusion, the wide dynamic range of HBV DNA quantitation achieved with the Abbott RealTime PCR assay makes it appropriate for the clinical monitoring of HBV infected patients. However, a change of HBV DNA quantitation method could influence results on the follow-up of HBV genotype C infected patients.Entities:
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Year: 2008 PMID: 18929599 DOI: 10.1016/j.jviromet.2008.09.014
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014