Volume 28, Issue 7 pp. 1003-1010
ORIGINAL ARTICLE

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

Gerrit Post

Gerrit Post

Department of Gastroenterology and Hepatology, Charité University Medical Center, Berlin, Germany

Center for Infectiology, Berlin, Germany

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Jess Howell

Jess Howell

Disease Elimination, Burnet Institute, Department of Gastroenterology, St. Vincent's Hospital, Department of Epidemiology and Preventive Medicine, Monash University Melbourne, Victoria, Australia

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Amina Sow

Amina Sow

Laboratoire de Bactériologie & Virologie, CHNU Dalal Jamm Guediawaye, IRESSEF Diamnoadio Dakar, Senegal

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Gibril Ndow

Gibril Ndow

Medical Research Council the Gambia unit (MRCG, London School of Hygiene and Tropical Medicine, Viral hepatitis Unit, Fajara, The Gambia

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Isabelle Chemin

Isabelle Chemin

INSERM U1052, CNRS 5286, Univ Lyon, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Université Claude Bernard Lyon 1, Lyon, France

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Gora Lo

Gora Lo

Laboratoire de Bactériologie & Virologie, CHNU Dalal Jamm Guediawaye, IRESSEF Diamnoadio Dakar, Senegal

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Amie Cessay

Amie Cessay

Medical Research Council the Gambia unit (MRCG, London School of Hygiene and Tropical Medicine, Viral hepatitis Unit, Fajara, The Gambia

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Damien Cohen

Damien Cohen

INSERM U1052, CNRS 5286, Univ Lyon, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Université Claude Bernard Lyon 1, Lyon, France

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Ramou Njie

Ramou Njie

International Agency for Research on Cancer (IARC, Lyon, France

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Souleymane Toure

Souleymane Toure

Unite de Formation et de Recherche (UFR) des sciences de la santé de l’Universite de Thies, Senegal

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Madoky Diop

Madoky Diop

Unite de Formation et de Recherche (UFR) des sciences de la santé de l’Universite de Thies, Senegal

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Roger Sombie

Roger Sombie

Service d’hépatogastro-entérologie, Centre Hospitalier Universitaire Yalgado Ouédraogo, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso

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Jean Nana

Jean Nana

Department of Hepatology & Gastroenterology, Université Grenoble Alpes, Grenoble, France

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Vincent Leroy

Vincent Leroy

Department of Hepatology & Gastroenterology, Université Grenoble Alpes, Grenoble, France

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Karine Lacombe

Karine Lacombe

Department of infectious diseases and tropical medicine, hôpital Saint-Antoine, SorbonneUniversité, Inserm IPLESP, APHP, Sorbonne, France

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Lamin Bojang

Lamin Bojang

Medical Research Council the Gambia unit (MRCG, London School of Hygiene and Tropical Medicine, Viral hepatitis Unit, Fajara, The Gambia

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Frank Tacke

Frank Tacke

Department of Gastroenterology and Hepatology, Charité University Medical Center, Berlin, Germany

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Coumba Toure-Kane

Coumba Toure-Kane

Laboratoire de Bactériologie & Virologie, CHNU Dalal Jamm Guediawaye, IRESSEF Diamnoadio Dakar, Senegal

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Mourtalla Ka

Mourtalla Ka

Unite de Formation et de Recherche (UFR) des sciences de la santé de l’Universite de Thies, Senegal

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Maimuna Mendy

Maimuna Mendy

International Agency for Research on Cancer (IARC, Lyon, France

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Souleymane Mboup

Souleymane Mboup

Laboratoire de Bactériologie & Virologie, CHNU Dalal Jamm Guediawaye, IRESSEF Diamnoadio Dakar, Senegal

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Mark Thursz

Mark Thursz

Department of Metabolism, Digestion and Reproduction, Division of Digestive Diseases, Hepatology Section, Imperial College London, St Mary’s campus, London, UK

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Yusuke Shimakawa

Yusuke Shimakawa

Unité d'Épidémiologie des Maladies Émergentes, Institut Pasteur, Paris, France

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Patrick Ingiliz

Patrick Ingiliz

Department of Gastroenterology and Hepatology, Charité University Medical Center, Berlin, Germany

Center for Infectiology, Berlin, Germany

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Maud Lemoine

Corresponding Author

Maud Lemoine

Department of Metabolism, Digestion and Reproduction, Division of Digestive Diseases, Hepatology Section, Imperial College London, St Mary’s campus, London, UK

Correspondence

Maud Lemoine, Imperial College London, Department of Metabolism, Digestion and Reproduction, Hepatology section, St Mary’s hospital, South Wharf Street, London, UK.

Email: [email protected]

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First published: 22 March 2021
Citations: 3

Funding information

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.

Abstract

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.

CONFLICTS OF INTEREST

ML, PI, YS and MT received research funding from Gilead US.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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