| Literature DB >> 33217778 |
Birgit Bremer1, Olympia E Anastasiou2, Svenja Hardtke3,4, Florin Alexandru Caruntu5, Manuela G Curescu6, Kendal Yalcin7, Ulus S Akarca8, Selim Gürel9, Stefan Zeuzem10, Andreas Erhardt11, Stefan Lüth12, George V Papatheodoridis13, Monica Radu5, Ramazan Idilman14, Michael P Manns1,4, Markus Cornberg1,4, Cihan Yurdaydin14,15, Heiner Wedemeyer1,4,16.
Abstract
The role of low levels of HDV-RNA during and after interferon therapy of hepatitis D is unknown. We re-analysed HDV RNA in 372 samples collected in the HIDIT-2 trial (Wedemeyer et al, Lancet Infectious Diseases 2019) with the Robogene assay (RA; Jena Analytics). Data were compared with the previously reported in-house assay (IA). We detected HDV-RNA in one-third of samples previously classified as undetectable using the highly sensitive RA. Low HDV viraemia detectable at week 48 or week 96 was associated with a high risk for post-treatment relapse, defined as HDV RNA positivity in both assays at week 120. HDV RNA relapses occurred in 10/15 (67%) patients with detectable low HDV RNA at week 48 and in 10/13 (77%) patients with low viraemia samples at week 96. In contrast, the post-treatment relapse rate was lower in patients with undetectable HDV RNA in both assays during treatment.Entities:
Keywords: HDV; Hepatitis D; PCR; relapse; residual viraemia
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Year: 2020 PMID: 33217778 DOI: 10.1111/liv.14740
Source DB: PubMed Journal: Liver Int ISSN: 1478-3223 Impact factor: 5.828