A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy

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 quality seroprevalence data fro...

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Main Authors: Downs, LO, Campbell, C, Yonga, P, Githinji, G, Ansari, MA, Matthews, PC, Etyang, AO
Format: Journal article
Language:English
Published: Public Library of Science 2023
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author Downs, LO
Campbell, C
Yonga, P
Githinji, G
Ansari, MA
Matthews, PC
Etyang, AO
author_facet Downs, LO
Campbell, C
Yonga, P
Githinji, G
Ansari, MA
Matthews, PC
Etyang, AO
author_sort Downs, LO
collection OXFORD
description 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 quality 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 studies 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 information 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.
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spelling oxford-uuid:2d7fd237-70de-40ac-bf48-040c1b7e168a2023-08-16T16:11:44ZA systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policyJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2d7fd237-70de-40ac-bf48-040c1b7e168aEnglishSymplectic ElementsPublic Library of Science2023Downs, LOCampbell, CYonga, PGithinji, GAnsari, MAMatthews, PCEtyang, AOThe 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 quality 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 studies 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 information 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.
spellingShingle Downs, LO
Campbell, C
Yonga, P
Githinji, G
Ansari, MA
Matthews, PC
Etyang, AO
A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title_full A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title_fullStr A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title_full_unstemmed A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title_short A systematic review of Hepatitis B virus (HBV) prevalence and genotypes in Kenya: data to inform clinical care and health policy
title_sort systematic review of hepatitis b virus hbv prevalence and genotypes in kenya data to inform clinical care and health policy
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