Evidence map›Paper›PMID 42082949›Full record

ArticleBMC infectious diseases2026

Local insights into hepatitis B Virus: genotype distribution and clinical profiles among HIV/HBV co-infected patients in Maputo, Mozambique.

Lucia Mabalane Chambal, Esperança Sevene, Charlotta Nilsson, Corssino Tchavana, Orvalho Augusto, José Luís João, Elias Manjate, Alice Manjate, João Piedade, Ricardo Parreira

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Lucia Mabalane ChambalFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique. luciachambal@gmail.com.
Esperança SeveneFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique.
Charlotta NilssonDivision of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, 17177, Sweden.
Corssino TchavanaManhiça Health Research Center (CISM), Manhiça, Maputo, Mozambique.
Orvalho AugustoFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique.
José Luís JoãoFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique.
Elias ManjateFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique.
Alice ManjateFaculty of Medicine, Eduardo Mondlane University, Av. Salvador Allende Nr. 702, Maputo, Mozambique.
João PiedadeGlobal Health and Tropical Medicine, GHTM, Associated Laboratory in Translation and Innovation Towards Global Health, LA-REAL, Instituto de Higiene e Medicina Tropical, IHMT, Universidade NOVA de Lisboa, UNL, Rua da Junqueira 100, Lisboa, 1349-008, Portugal.
Ricardo ParreiraGlobal Health and Tropical Medicine, GHTM, Associated Laboratory in Translation and Innovation Towards Global Health, LA-REAL, Instituto de Higiene e Medicina Tropical, IHMT, Universidade NOVA de Lisboa, UNL, Rua da Junqueira 100, Lisboa, 1349-008, Portugal.

Funding

Swedish International Development Cooperation Agency 51140073
6 · The paper itself

Abstract

introductionHepatitis B virus (HBV) coinfection worsens HIV care outcomes and liver disease risk, but genotype-specific data in the World Health Organization (WHO) Africa Region is limited. To address this gap, we assessed HBV genotype distribution and genotype-specific clinical features in a cohort of people living with HIV (PLHIV) in Maputo City, Mozambique.

methodsThis was a sub-analysis of a prospective cohort study that included newly diagnosed, HIV/HBV coinfected patients who were enrolled from May 2021 to November 2023. DNA extraction and partial-genome nested PCR with Sanger sequencing was performed on plasma samples. HBV genotypes were assigned by BLASTn, Geno2pheno, HBVdb, and NCBI-HBV, and phylogeny was inferred with MAFFT-based alignments and maximum likelihood-based phylogenetics. Clinical/laboratory data (Hepatitis B e antigen, HBV viral load, aspartate aminotransferase, alanine aminotransferase, CD4

resultsOf 1,106 newly diagnosed ART-naïve PLHIV, 81 (7.3%) were hepatitis B surface antigen (HBsAg)-positive and genotyping was successful in 55 (68%). Among HBV genotyped patients, the median age was 33.0 years (IQR 30.0, 39.0), 37 (67.3%) were male, 46 (83.6%) had HBV genotype A (subgenotype A1) and 9 (16.4%) genotype E. Median AST, ALT, and APRI scores tended to be higher in genotype E than subgenotype A1 cases, although differences were not statistically significant (AST 71.9 vs. 37.9 U/L; IQR 26.0-118.0 vs. 29.0-98.1; ALT 36.5 vs. 32.6 U/L; IQR 20.4-63.0 vs. 20.2-57.7; APRI 1.3 vs. 0.5; IQR 0.3-1.8 vs. 0.3-1.3). HBV DNA > 2,000 IU/mL occurred in 52.2% of subgenotype A1 and 55.6% of genotype E cases. Most cases were HBeAg-negative (A1: 36/46, 78.3%; E: 6/9, 66.7%).

conclusionHBV subgenotype A1 and genotype E are prevalent among HIV/HBV coinfected patients in Maputo, often with high HBV DNA levels and evidence of liver injury. Routine HBV screening, simple fibrosis assessment and further research are recommended.

Indexed as

CoinfectionGenotypeHepatitis BHepatitis B virusHIV InfectionsAdultDNA, ViralFemaleHumansMaleMiddle AgedMozambiquePhylogenyProspective StudiesViral LoadDNA, ViralFibrosisHBV genotypesHepatitis B virusHIVMaputoMozambique

Identifiers

PMID42082949
PMCPMC13289236

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.