Evidence map›Paper›PMID 40412394›Full record

ArticleThe Lancet. Global health2025

Identifying gaps in the HIV treatment cascade in Africa: a model comparison study.

Loveleen Bansi-Matharu, Haroon Moolla, Daniel T Citron, John Stover, Michael Pickles, Rowan Martin-Hughes, Marie-Claude Boily, Rose Nyirenda, Edinah Mudimu, Debra Ten Brink and 10 more

Abstract readComparative Study
In one paragraph

Article in The Lancet. Global health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The HIV/AIDS pandemic: where are we now?AIDS (London, England) · 2025
    Article
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

20 authors.

Loveleen Bansi-MatharuUCL Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, UK. Electronic address: l.bansi-matharu@ucl.ac.uk.
Haroon MoollaCentre for Infectious Disease Epidemiology and Research, University of Cape Town, Cape Town, South Africa.
Daniel T CitronDepartment of Population Health, New York University Grossman School of Medicine, New York, NY, USA.
John StoverAvenir Health, Takoma Park, MD, USA.
Michael PicklesDepartment of Infectious Disease Epidemiology, Imperial College London, London, UK.
Rowan Martin-HughesBurnet Institute, Melbourne, VIC, Australia.
Marie-Claude BoilyMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Rose NyirendaDepartment of HIV and AIDS, Ministry of Health Malawi, Lilongwe, Malawi.
Edinah MudimuDepartment of Decision Sciences, University of South Africa, Pretoria, South Africa.
Debra Ten BrinkBurnet Institute, Melbourne, VIC, Australia.
Leigh F JohnsonCentre for Infectious Disease Epidemiology and Research, University of Cape Town, Cape Town, South Africa.
Owen MugurungiMinistry of Health & Child Welfare, Harare, Zimbabwe.
Valentina CambianoUCL Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, UK.
Dobromir DimitrovPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jenny SmithUCL Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, UK.
Robert GlaubiusCenter for Modeling, Planning and Policy Analysis, Avenir Health, Glastonbury, CT, USA.
Issac TaramusiUNAIDS Country Office Zimbabwe, Harare, Zimbabwe.
Amon MpofuNational AIDS Council, Harare, Zimbabwe.
Andrew PhillipsUCL Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, UK.
Anna BershteynDepartment of Population Health, New York University Grossman School of Medicine, New York, NY, USA.

Funding

SDMC: HPTN 084 Pregnancy SupplementUM1AI068617 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Elizabeth Renata Brown, Deborah J Donnell · 2011 to 2026
$204.9M
NIAID NIH HHS UM1 AI068617Wellcome Trust
6 · The paper itself

Abstract

backgroundAlthough HIV incidence has considerably decreased in eastern, central, and southern Africa, new HIV infections continue to be a major public health challenge in the region. We aimed to investigate where in the HIV treatment cascade new transmissions are occurring in Malawi, Zimbabwe, and South Africa (the three countries involved in the Modelling to Inform HIV Programmes in Sub-Saharan Africa project).

methodsIn this model comparison study, we used six well described and independently calibrated HIV transmission dynamics models that have been used to inform HIV policy in Africa (Optima HIV, EMOD, Goals, Thembisa, PopART-IBM, and HIV Synthesis) to estimate and predict the proportion of annual new HIV transmissions attributable to people living with HIV who are undiagnosed, have been diagnosed but have not yet started antiretroviral therapy (ART), are receiving ART, and have interrupted ART in Malawi, Zimbabwe, and South Africa from 2010 to 2040 stratified by the age and sex of the individual acquiring HIV.

findingsDespite the different model structures and underlying assumptions, the six models were well aligned in relation to key HIV epidemic characteristics (including population estimates and HIV prevalence) in each of the three settings. There was, however, considerable variation in the predicted number of new infections, particularly in Malawi and Zimbabwe where this number ranged from fewer than 10 000 new infections to over 30 000 new infections in 2024. Most model results suggested that the mean age of HIV acquisition has been increasing since 2000, with men acquiring HIV at an older age than women in all three settings. All models attributed fewer than 5% of transmissions to individuals who had been diagnosed but had not yet started ART. In Malawi, the proportion of transmissions attributable to undiagnosed people with HIV in 2024 ranged from 33·3% to 75·3% across the models, and transmissions attributable to individuals who had experienced interrupted treatment ranged from 8·4% to 20·1%. In Zimbabwe, the proportion of transmissions attributable to undiagnosed individuals in 2024 ranged from 29·8% to 64·6% across the models and the proportion of transmissions attributable to individuals who had interrupted treatment ranged from 4·7% to 21·5%. In South Africa, 21·8-46·4% of transmissions in 2024 were attributable to undiagnosed individuals and 27·6-58·9% of transmissions were attributable to individuals who had interrupted treatment.

interpretationAcross the three study settings, a substantial proportion of new HIV transmissions were attributable to undiagnosed individuals and people who have received interrupted ART, reinforcing the importance of continuing HIV testing and ART re-engagement and retention interventions.

fundingThe Bill & Melinda Gates Foundation.

Indexed as

Anti-HIV AgentsHIV InfectionsAdolescentAdultAfricaFemaleHumansIncidenceMalawiMaleMiddle AgedPrevalenceSouth AfricaYoung AdultZimbabweAnti-HIV Agents

Identifiers

PMID40412394
PMCPMC12500161

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.