RESEARCH ARTICLE
A systematic review of Hepatitis B virus (HBV)
prevalence and genotypes in Kenya: Data to
inform clinical care and health policy
Louise O. Downs
ID
1,2
, Cori Campbell
1
, Paul Yonga
ID
3
, George Githinji
4,5
, M.
Azim Ansari ID
1
, Philippa C. MatthewsID
1,6,7,8☯
*, Anthony O. Etyang
4☯
1 Nuffield Department of Medicine, Medawar Building for Pathogen Research, University of Oxford, Oxford,
United Kingdom, 2 Department of Infectious Diseases and Microbiology, John Radcliffe Hospital, Headley
Way, Oxford, United Kingdom, 3 CA Medlynks Clinic and Laboratory, Nairobi, and Fountain Projects and
Research Office, Fountain Health Care Hospital, Eldoret, Kenya, 4 KEMRI-Wellcome Trust Research
Programme, Kilifi, Kenya, 5 Department of Biochemistry and Biotechnology, Pwani University, Kilifi, Kenya,
6 The Francis Crick Institute, London, United Kingdom, 7 Division of Infection and Immunity, University
College London, London, London, United Kingdom, 8 Department of Infectious Diseases, University College
London Hospital, London, London, United Kingdom
☯ These authors contributed equally to this work.
* philippa.matthews@crick.ac.uk
Abstract
The aim of this systematic review and meta-analysis is to evaluate available prevalence and
viral sequencing data representing chronic hepatitis B (CHB) infection in Kenya. More than
20% of the global disease burden from CHB is in Africa, however there is minimal high qual-
ity seroprevalence data from individual countries and little viral sequencing data available to
represent the continent. We undertook a systematic review of the prevalence and genetic
data available for hepatitis B virus (HBV) in Kenya using the Preferred Reporting Items for
Systematic Review and Meta-analysis (PRISMA) 2020 checklist. We identified 23 studies
reporting HBV prevalence and 8 studies that included HBV genetic data published in English
between January 2000 and December 2021. We assessed study quality using the Joanna
Briggs Institute critical appraisal checklist. Due to study heterogeneity, we divided the stud-
ies to represent low, moderate, high and very high-risk for HBV infection, identifying 8, 7, 5
and 3 studies in these groups, respectively. We calculated pooled HBV prevalence within
each group and evaluated available sequencing data. Pooled HBV prevalence was 3.4%
(95% CI 2.7–4.2%), 6.1% (95% CI 5.1–7.4%), 6.2% (95% CI 4.64–8.2) and 29.2% (95% CI
12.2–55.1), respectively. Study quality was overall low; only three studies detailed sample
size calculation and 17/23 studies were cross sectional. Eight studies included genetic infor-
mation on HBV, with two undertaking whole genome sequencing. Genotype A accounted
for 92% of infections. Other genotypes included genotype D (6%), D/E recombinants (1%)
or mixed populations (1%). Drug resistance mutations were reported by two studies. There
is an urgent need for more high quality seroprevalence and genetic data to represent HBV in
Kenya to underpin improved HBV screening, treatment and prevention in order to support
progress towards elimination targets.
PLOS GLOBAL PUBLIC HEALTH
PLOS Global Public Health | https://doi.org/10.1371/journal.pgph.0001165 January 31, 2023 1 / 20
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OPEN ACCESS
Citation: Downs LO, Campbell C, Yonga P, Githinji
G, Ansari MA, Matthews PC, et al. (2023) A
systematic review of Hepatitis B virus (HBV)
prevalence and genotypes in Kenya: Data to inform
clinical care and health policy. PLOS Glob Public
Health 3(1): e0001165. https://doi.org/10.1371/
journal.pgph.0001165
Editor: Abraham D. Flaxman, University of
Washington, UNITED STATES
Received: May 31, 2022
Accepted: November 28, 2022
Published: January 31, 2023
Peer Review History: PLOS recognizes the
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editorial history of this article is available here:
https://doi.org/10.1371/journal.pgph.0001165
Copyright: © 2023 Downs et al. This is an open
access article distributed under the terms of the
Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.
Data Availability Statement: All the data pertinent
to the submission are included in the paper and its
citations.