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. 2023 Jan 31;3(1):e0001165.
doi: 10.1371/journal.pgph.0001165. eCollection 2023.

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

Affiliations

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

Louise O Downs et al. PLOS Glob Public Health. .

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 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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Conflict of interest statement

I have read the journal’s policy and the authors of this manuscript have the following competing interests: CC is partially funded by GlaxoSmithKline. There are no patents, products in development or marketed products associated with this research to declare. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Figures

Fig 1
Fig 1. Flow chart for eligibility of studies included in a systematic review reporting prevalence and genetic data for HBV in Kenya between 2000–2021.
(AJOL: African Journal Online). All eight studies included for genetic analysis contain information on HBV genotype. Figure created in Biorender.com with licence to publish.
Fig 2
Fig 2. Map of Kenya indicating the locations and size of populations from which seroprevalence of HBV infection is reported.
Data from a systematic review of papers reporting prevalence and genetic data for HBV in Kenya between 2000 and 2021. The size of the red circle indicates numbers screened in each location, studies in the same location are grouped together. n = number of individuals reported. Surrounding countries are marked in blue, Kenya’s four most populous cities are marked in black. Figure created using R version 4.2.0, packages ggmaps version 3.0.0, ggplot2 version 3.3.6 and sf version 1.0–7. The Kenyan county shapefiles were obtained from the Humanitarian Data Exchange, available open source from https://data.humdata.org/dataset/geoboundaries-admin-boundaries-for-kenya.
Fig 3
Fig 3. Bar chart showing characteristics of studies identified for a systematic review reporting prevalence and genetic data for HBV in Kenya.
This is stratified by number of participants, study design, sampling method, data collection and diagnostic methods. RCT: Randomised controlled trial; EIA: Chemiluminescent enzyme immunoassay; ELISA: Enzyme linked immunosorbent assay.
Fig 4
Fig 4. Forest plot showing pooled HBV prevalence for populations in different risk groups by random effects model.
Data generated through a systematic review reporting prevalence and genetic data for HBV in Kenya between 2000–2021. In each case, the size of the population included is represented by the size of the square. Point prevalence and 95% Confidence Interval (CI) is indicated for each study. Studies are ordered by HBV prevalence in each risk group.
Fig 5
Fig 5. Maximum likelihood phylogenetic tree of full-length consensus HBV sequences from Kenya.
Kenyan sequences are those published in GenBank (downloaded 1st Dec 2021) and are shown in red alongside genotype reference sequences in black (1000 bootstrap replicates were performed, and bootstrap support of ≥70% are indicated. Reference sequences from McNaughton et al. (2020) [11].

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