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Clinical utility of quantifying hepatitis B surface antigen in African patients with chronic hepatitis B

Authors :
Frank Tacke
Gora Lo
Ka Mm
Vincent Leroy
Amina Sow
Madoky Magatte Diop
Yusuke Shimakawa
J. Howell
Lamin Bojang
Souleymane Toure
P. Ingiliz
Damien Cohen
Karine Lacombe
Gerrit Post
Maud Lemoine
Ramou Njie
Souleymane Mboup
Gibril Ndow
Maimuna Mendy
Amie Cessay
Isabelle Chemin
Coumba Toure-Kane
Mark Thursz
Jean Nana
Roger Sombié
Charité - UniversitätsMedizin = Charité - University Hospital [Berlin]
Monash University [Melbourne]
Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL)
Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Centre International de Recherche contre le Cancer - International Agency for Research on Cancer (CIRC - IARC)
Organisation Mondiale de la Santé / World Health Organization Office (OMS / WHO)
Université de Thiès
Université Joseph Ki-Zerbo [Ouagadougou] (UJZK)
Université Grenoble Alpes (UGA)
Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)
Imperial College London
Epidémiologie des Maladies Emergentes - Emerging Diseases Epidemiology
Pasteur-Cnam Risques infectieux et émergents (PACRI)
Institut Pasteur [Paris]-Conservatoire National des Arts et Métiers [CNAM] (CNAM)
HESAM Université (HESAM)-HESAM Université (HESAM)-Institut Pasteur [Paris]-Conservatoire National des Arts et Métiers [CNAM] (CNAM)
HESAM Université (HESAM)-HESAM Université (HESAM)
The PROLIFICA project (www.prolifica.africa) was funded was the EC FP7 (2011-2016) and is currently funded by the MRC UK and received support from Gilead US company.
The authors thank Echosens, France, for their support
they are also grateful to all the patients and their families.
Institut Pasteur [Paris] (IP)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)
HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-Institut Pasteur [Paris] (IP)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)
HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)
Source :
Journal of Viral Hepatitis, Journal of Viral Hepatitis, Wiley-Blackwell, 2021, 28 (7), pp.1003-1010. ⟨10.1111/jvh.13499⟩, Journal of Viral Hepatitis, 2021, 28 (7), pp.1003-1010. ⟨10.1111/jvh.13499⟩
Publication Year :
2021

Abstract

International audience; The clinical utility of quantifying hepatitis B surface antigen (qHBsAg) levels in African subjects with chronic hepatitis B virus (HBV) infection has been poorly documented. From a multicentre cohort of 944 HBV-infected African patients, we aimed to assess whether qHBsAg alone can accurately identify i) those in a HBeAg-negative chronic HBV infection phase at low risk of liver disease progression and ii) those in need of antiviral therapy according to the 2017 EASL guidelines. We analysed 770 HBV mono-infected treatment-naïve patients, mainly males (61%) from West Africa (92%), median age 35 years (IQR: 30-44), median HBV DNA: 95.6 IU/ml (10.0-1,300.0), median qHBsAg 5,498 IU/ml (1,171-13,000) and HBeAg-pos 38 (5%). A total of 464/770 (60.2%) patients were classified as HBeAg-negative chronic infection (median age 36 years (31-46), median ALT 23 IU/l (18-28), median HBV-DNA 33.5 IU/ml (3.8-154.1), median LSM 4.8 kPa (4.1-5.8)) and qHBsAg levels had poor accuracy to identify these subjects with an AUROC at 0.58 (95%CI: 0.54-0.62), sensitivity 55.0% and specificity 55.6%; 118/770 (15.3%) patients were eligible for treatment according to the 2017 EASL criteria. qHBsAg correlated poorly with HBV DNA and had poor accuracy to select patients for antiviral therapy with an AUROC at 0.54 (0.49-0.60), sensitivity 46.6% and specificity 46.9%. In African treatment-naïve HBV-infected subjects, the clinical utility of qHBsAg to identify subjects in HBeAg-negative infection phase or subjects eligible for antiviral therapy seems futile. Whether qHBsAg levels can be used as a predictor of long-term liver complications in Africa needs to be further investigated.

Details

ISSN :
13652893 and 13520504
Volume :
28
Issue :
7
Database :
OpenAIRE
Journal :
Journal of viral hepatitisREFERENCES
Accession number :
edsair.doi.dedup.....bb190c8c42fb5d96014e163925f15421