Publication:
HBV RNA levels are associated with virological response to treatment with pegylated interferon alpha in patients with chronic hepatitis D virus infection

dc.contributor.coauthorSandmann, Lisa
dc.contributor.coauthorBremer, Birgit
dc.contributor.coauthorDeterding, Katja
dc.contributor.coauthorManns, Michael P.
dc.contributor.coauthorCornberg, Markus
dc.contributor.coauthorWedemeyer, Heiner
dc.contributor.coauthorMaasoumy, Benjamin
dc.contributor.kuauthorYurtaydın, Süleyman Cihan
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid189330
dc.date.accessioned2024-11-09T23:12:05Z
dc.date.issued2022
dc.description.abstractStandard treatment of hepatitis delta virus (HDV) infection remains pegylated-interferon alfa (peg-IFNα) in most centers, which is not only associated with rather low efficacy but several adverse events. Hepatitis B core-related antigen (HBcrAg) is linked to intrahepatic covalently closed circular DNA levels and has previously been suggested as response predictor in IFN-based treatment of hepatitis B virus (HBV) mono-infection. This study aimed to investigate the value of HBcrAg in the management of patients with HBV/HDV co-infection undergoing peg-IFNα treatment. The Hep-Net-International-Delta-Hepatitis-Intervention Trial-2 study included 120 patients co-infected with HBV/HDV. Patients were treated for 96 weeks with peg-IFNα and either tenofovir or placebo. Ninety-nine patients with HDV-RNA results 24 weeks after end of treatment (FU24) were included in this analysis, of whom 32 patients (32.3%) had undetectable HDV RNA at FU24. HBcrAg was measured at baseline, week 12, 24, 48, 96, and FU24. HBcrAg levels showed no significant correlation with HDV RNA but were significantly linked to treatment outcome. HBcrAg levels < 4.5 log IU/mL at baseline, week 24, and week 48 had high negative predictive value (NPV) for achieving undetectable HDV RNA at FU24 (81.8%, 87.1% and 95.0%, respectively). Similarly, HBcrAg levels at week 96 were significantly higher in patients with viral relapse until FU24 (3.0 vs. 3.63 log IU/mL; P = 0.0089). Baseline, week 24, and week 48 HBcrAg levels were also associated with the likelihood of achieving HBsAg level < 100 IU/mL at FU24 (HBcrAg < 3.0 log IU/mL: NPV 91.7%, 90.4% and 92.3%, respectively). Test statistics improved when combining HBcrAg with additional viral and clinical parameters. Conclusion: HBcrAg is linked to treatment response to peg-IFNα in patients with HBV/HDV co-infection and could be a promising marker to determine treatment futility.
dc.description.indexedbyWoS
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.volume77
dc.identifier.doiN/A
dc.identifier.eissn1600-0641
dc.identifier.issn0168-8278
dc.identifier.quartileQ1
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9758
dc.identifier.wos826275104199
dc.keywordsHBV RNA levels
dc.keywordsVirological response
dc.keywordsInterferon alpha
dc.keywordsChronic Hepatitis D virus infection
dc.languageEnglish
dc.publisherElsevier
dc.sourceJournal of Hepatology
dc.subjectGastroenterology
dc.subjectHepatology
dc.titleHBV RNA levels are associated with virological response to treatment with pegylated interferon alpha in patients with chronic hepatitis D virus infection
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.authorid0000-0002-5419-7158
local.contributor.kuauthorYurtaydın, Süleyman Cihan

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