Caucasian Ethnicity, but Not Treatment Cessation is Associated with HBsAg Loss Following Nucleos(t)ide Analogue-Induced HBeAg Seroconversion.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
26 07 2019
Historique:
received: 27 06 2019
revised: 17 07 2019
accepted: 25 07 2019
entrez: 31 7 2019
pubmed: 31 7 2019
medline: 26 9 2020
Statut: epublish

Résumé

It is well appreciated that ethnicity influences the natural history and immune responses during a chronic hepatitis B infection. In this study, we explore the effect of ethnicity and treatment cessation on Hepatitis B surface Antigen (HBsAg) seroclearance in patients with Nucleos(t)ide Analogue (NA)-induced Hepatitis B e Antigen (HBeAg) seroconversion. We performed a multi-ethnic, multicentric observational cohort study. The analyzed cohort consisted of 178 mono-infected, predominantly male (75.3%) chronic hepatitis B patients of mixed ethnicity (44.4% Asians, 48.9% Caucasians) with nucleos(t)ide analogue-induced HBeAg seroconversion. Treatment was withdrawn in 105 patients and continued in 73, leading to HBsAg loss in 14 patients off- and 16 patients on-treatment, respectively. Overall, HBsAg loss rates were not affected by treatment cessation (hazard ratio 1.45,

Identifiants

pubmed: 31357522
pii: v11080687
doi: 10.3390/v11080687
pmc: PMC6723144
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Hepatitis B Surface Antigens 0
Nucleosides 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

T. Vanwolleghem is recipient of a 2014 mandate from the Belgian Foundation Against Cancer (mandate number: 2014-087) and received research funding from Gilead Sciences, Bristol-Myers-Squib (BMS) and Roche Diagnostics. C. Moreno acted as consultant and received research grants from BMS and Gilead. H. Van Vlierberghe received research grants from Gilead and BMS. B. Hansen has received grants from and is consultant for Intercept Pharmaceuticals. H.L.A. Janssen has received grants from and is consultant for Abbott, Bristol-Myers Squibb, Gilead Sciences, Merck, Novartis, Roche, and Janssen. S. Van Hees, H. Chi, S. Bourgeois, T. Sersté, S. Francque, D. Wong, D. Sprengers and F. Nevens declare no conflicts of interest.

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Auteurs

Stijn Van Hees (S)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, 2650 Antwerp, Belgium.
Laboratory of Experimental Medicine and Pediatrics, University of Antwerp, 2650 Antwerp, Belgium.

Heng Chi (H)

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, 3015 AA Rotterdam, The Netherlands.

Bettina Hansen (B)

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, 3015 AA Rotterdam, The Netherlands.
Toronto Centre of Liver Disease, University Health Network, Toronto General Hospital, University of Toronto, Toronto, ON M5G2C4, Canada.

Stefan Bourgeois (S)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, 2650 Antwerp, Belgium.
Department of Gastroenterology and Hepatology, ZNA Stuivenberg, 2060 Antwerp, Belgium.

Hans Van Vlierberghe (H)

Department of Gastroenterology and Hepatology, Ghent University Hospital, 9000 Ghent, Belgium.

Thomas Sersté (T)

Department of Gastroenterology and Hepatology, Saint-Pierre University Hospital, 1000 Brussels, Belgium.

Sven Francque (S)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, 2650 Antwerp, Belgium.
Laboratory of Experimental Medicine and Pediatrics, University of Antwerp, 2650 Antwerp, Belgium.

David Wong (D)

Toronto Centre of Liver Disease, University Health Network, Toronto General Hospital, University of Toronto, Toronto, ON M5G2C4, Canada.

Dirk Sprengers (D)

Department of Gastroenterology and Hepatology, GZA Antwerp, 2610 Antwerp, Belgium.

Christophe Moreno (C)

Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Hôpital Erasme, Université Libre de Bruxelles, 1050 Brussels, Belgium.

Frederik Nevens (F)

Department of Hepatology, University Hospitals KULeuven, 3000 Leuven, Belgium.

Harry Janssen (H)

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, 3015 AA Rotterdam, The Netherlands.
Toronto Centre of Liver Disease, University Health Network, Toronto General Hospital, University of Toronto, Toronto, ON M5G2C4, Canada.

Thomas Vanwolleghem (T)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, 2650 Antwerp, Belgium. Thomas.vanwolleghem@uza.be.
Laboratory of Experimental Medicine and Pediatrics, University of Antwerp, 2650 Antwerp, Belgium. Thomas.vanwolleghem@uza.be.
Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, 3015 AA Rotterdam, The Netherlands. Thomas.vanwolleghem@uza.be.

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