Publication: Residual low HDV viraemia is associated HDV RNA relapse after PEG-IFNa-based antiviral treatment of hepatitis delta: Results from the HIDIT-II study
dc.contributor.author | Bremer, Birgit | |
dc.contributor.author | Anastasiou, Olympia E. | |
dc.contributor.author | Hardtke, Svenja | |
dc.contributor.author | Caruntu, Florin A. | |
dc.contributor.author | Curescu, Manuela G. | |
dc.contributor.author | Yalçın, Kendal | |
dc.contributor.author | Akarca, Ulus S. | |
dc.contributor.author | Zeuzem, Stefan | |
dc.contributor.author | Erhardt, Andreas | |
dc.contributor.author | Luth, Stefan | |
dc.contributor.author | Papatheodoridis, George V. | |
dc.contributor.author | Radu, Monica | |
dc.contributor.author | İdilman, Ramazan | |
dc.contributor.author | Manns, Michael P. | |
dc.contributor.author | Cornberg, Markus | |
dc.contributor.author | Yurdaydın, Cihan | |
dc.contributor.author | Wedemeyer, Heiner | |
dc.contributor.buuauthor | Gürel, Selim | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları. | tr_TR |
dc.contributor.researcherid | HLH-8209-2023 | |
dc.contributor.scopusid | 7003706434 | tr_TR |
dc.date.accessioned | 2024-02-27T13:16:01Z | |
dc.date.available | 2024-02-27T13:16:01Z | |
dc.date.issued | 2020-11-20 | |
dc.description.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. | en_US |
dc.description.sponsorship | Roche | en_US |
dc.description.sponsorship | Gilead Sciences | en_US |
dc.description.sponsorship | AbbVie | en_US |
dc.description.sponsorship | Berlin Mathematical School | en_US |
dc.identifier.citation | Bremer, B. vd. (2020). "Residual low HDV viraemia is associated HDV RNA relapse after PEG-IFNa-based antiviral treatment of hepatitis delta: Results from the HIDIT-II study". Liver International, 41(2), 295-299. | en_US |
dc.identifier.doi | https://doi.org/10.1111/liv.14740 | |
dc.identifier.endpage | 299 | tr_TR |
dc.identifier.issn | 1478-3223 | |
dc.identifier.issn | 1478-3231 | |
dc.identifier.issn | https://onlinelibrary.wiley.com/doi/10.1111/liv.14740 | |
dc.identifier.issue | 2 | tr_TR |
dc.identifier.pubmed | 33217778 | |
dc.identifier.scopus | 2-s2.0-85097085763 | |
dc.identifier.startpage | 295 | tr_TR |
dc.identifier.uri | https://hdl.handle.net/11452/40013 | |
dc.identifier.volume | 41 | tr_TR |
dc.identifier.wos | 000595714300001 | |
dc.indexed.pubmed | PubMed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.journal | Liver International | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | HDV | en_US |
dc.subject | Hepatitis D | en_US |
dc.subject | PCR | en_US |
dc.subject | Relapse | en_US |
dc.subject | Residual viraemia | en_US |
dc.subject | Virus-RNA | en_US |
dc.subject | Quantification | en_US |
dc.subject | Gastroenterology & hepatology | en_US |
dc.subject.emtree | Alanine aminotransferase | en_US |
dc.subject.emtree | Aspartate aminotransferase | en_US |
dc.subject.emtree | Peginterferon alpha2a | en_US |
dc.subject.emtree | Tenofovir disoproxil | en_US |
dc.subject.emtree | Virus RNA | en_US |
dc.subject.emtree | Antiviral therapy | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Combination drug therapy | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Disease association | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Hepatitis D | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Infection risk | en_US |
dc.subject.emtree | Limit of detection | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Null result | en_US |
dc.subject.emtree | Predictive value | en_US |
dc.subject.emtree | Recurrence risk | en_US |
dc.subject.emtree | RNA analysis | en_US |
dc.subject.emtree | Viremia | en_US |
dc.subject.emtree | Virus load | en_US |
dc.subject.scopus | Hepatitis Delta Virus; Chronic Hepatitis D; Hepatitis B | en_US |
dc.subject.wos | Gastroenterology & hepatology | en_US |
dc.title | Residual low HDV viraemia is associated HDV RNA relapse after PEG-IFNa-based antiviral treatment of hepatitis delta: Results from the HIDIT-II study | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication |
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