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dc.creatorPapatheodoridi M., Papachristou E., Moschidis Z., Hadziyannis E., Rigopoulou E., Zachou K., Villeret F., Magiorkinis G., Lyberopoulou A., Gatselis N., Vlachogiannakos I., Manolakopoulos S., Dalekos G.N., Zoulim F., Paraskevis D., Papatheodoridis G.V.en
dc.date.accessioned2023-01-31T09:44:50Z
dc.date.available2023-01-31T09:44:50Z
dc.date.issued2022
dc.identifier10.1111/jvh.13729
dc.identifier.issn13520504
dc.identifier.urihttp://hdl.handle.net/11615/77857
dc.description.abstractHBV RNA is considered as a promising predictor in patients who discontinue nucleos(t)ide analogues (NAs). We determined HBV RNA levels in non-cirrhotic HBeAg-negative patients who discontinued NAs and assessed their predictability for 12-month outcomes. Fifty-seven patients of DARING-B study were included. HBV RNA levels were determined in stored monthly serum samples drawn at 0–3 months after end of therapy (EOT). Other markers previously determined in the same cohort including hepatitis B core-related antigen (HBcrAg) were also assessed. HBV RNA at EOT was detectable in 7% of patients, who developed virological/clinical relapse and required retreatment at month 2; in patients with undetectable EOT HBV RNA, 12-month cumulative rates of virological relapse, clinical relapse and retreatment were 68%, 28% and 21%, respectively (p ≤ 0.008). HBV RNA at month-1 after EOT was detectable in 19% of patients being associated with higher probability only of virological relapse (p = 0.001). HBV RNA levels correlated significantly to HBV DNA, HBcrAg, ALT and interferon-induced protein-10, but not HBsAg levels. Combined EOT HBV RNA and HBcrAg detection and/or HBsAg >1000 IU/ml was associated only with higher probability of retreatment having higher sensitivity and lower specificity than HBV RNA alone. In conclusion, serum HBV RNA is detectable in a minority of non-cirrhotic HBeAg-negative patients under effective long-term NAs therapy offering low sensitivity but 100% specificity for early retreatment due to severe clinical relapses after NA discontinuation. The combinations of EOT HBV RNA with HBcrAg and/or high HBsAg levels increase sensitivity but decrease specificity for prediction of retreatment after NAs withdrawal. © 2022 John Wiley & Sons Ltd.en
dc.language.isoenen
dc.sourceJournal of Viral Hepatitisen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85136849037&doi=10.1111%2fjvh.13729&partnerID=40&md5=752adb9c75475d9bf8883f482e202312
dc.subjectalanine aminotransferaseen
dc.subjectantivirus agenten
dc.subjectgamma interferon inducible protein 10en
dc.subjecthepatitis B core antigenen
dc.subjecthepatitis B(e) antigenen
dc.subjectvirus RNAen
dc.subjectantivirus agenten
dc.subjecthepatitis B core antigenen
dc.subjecthepatitis B surface antigenen
dc.subjecthepatitis B(e) antigenen
dc.subjectinterferonen
dc.subjectRNAen
dc.subjectvirus DNAen
dc.subjectantiviral therapyen
dc.subjectArticleen
dc.subjectblood samplingen
dc.subjectchronic hepatitis Ben
dc.subjectcohort analysisen
dc.subjectdisease courseen
dc.subjectdrug efficacyen
dc.subjecthumanen
dc.subjectlong term careen
dc.subjectmajor clinical studyen
dc.subjectpredictionen
dc.subjectrecurrent diseaseen
dc.subjectretrospective studyen
dc.subjectRNA blood levelen
dc.subjectsensitivity and specificityen
dc.subjecttreatment durationen
dc.subjecttreatment withdrawalen
dc.subjectchronic hepatitis Ben
dc.subjectgeneticsen
dc.subjectHepatitis B virusen
dc.subjectAntiviral Agentsen
dc.subjectDNA, Viralen
dc.subjectHepatitis B Core Antigensen
dc.subjectHepatitis B e Antigensen
dc.subjectHepatitis B Surface Antigensen
dc.subjectHepatitis B virusen
dc.subjectHepatitis B, Chronicen
dc.subjectHumansen
dc.subjectInterferonsen
dc.subjectRecurrenceen
dc.subjectRNAen
dc.subjectJohn Wiley and Sons Incen
dc.titleSignificance of serum HBV RNA in non-cirrhotic HBeAg-negative chronic hepatitis B patients who discontinue effective antiviral therapyen
dc.typejournalArticleen


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