Evidence map›Paper›PMID 41892690›Full record

Trial reportJournal of the Pediatric Infectious Diseases Society2026

Brain Structure of South African Children Born to Mothers on Dolutegravir Versus Efavirenz-Based Antiretroviral Therapy.

Layla E Bradford, Catherine J Wedderburn, Thokozile R Malaba, Helene Theunissen, Jessica E Ringshaw, Niall J Bourke, Steve C R Williams, Nengjie He, Lucy Read, Catriona Waitt and 10 more

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Journal of the Pediatric Infectious Diseases Society, 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

20 authors.

Layla E BradfordDepartment of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.ORCID 0000-0002-5195-9081
Catherine J WedderburnDepartment of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.
Thokozile R MalabaDivision of Epidemiology & Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.
Helene TheunissenDivision of Epidemiology & Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.
Jessica E RingshawDepartment of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.
Niall J BourkeDepartment of Neuroimaging, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Steve C R WilliamsDepartment of Neuroimaging, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Nengjie HeGlobal Health Trials Unit, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Lucy ReadGlobal Health Trials Unit, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Catriona WaittInfectious Diseases Institute, Makerere University, Kampala, Uganda.ORCID 0000-0003-0134-5855
Helen ReynoldsDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, United Kingdom.
Angela ColbersDepartment of Pharmacy, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0002-0389-9934
Jim ReadGlobal Health Trials Unit, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Lauren DavelDepartment of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.
Catherine OrrellDesmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.
Miriam TaegtmeyerDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Duolao WangDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Saye KhooDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, United Kingdom.
Landon MyerDivision of Epidemiology & Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.
Kirsten A DonaldDepartment of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.

Funding

Commonwealth & Development OfficeEuropean UnionGates Foundation INV-023509Science for Africa Foundation Del-22-002UNITAID 2016-08-UoLWellcome Trust 224 287/Z/21/ZWellcome Trust and the UK Foreign
6 · The paper itself

Abstract

backgroundThe impact of in utero exposure to specific antiretroviral therapy (ART), particularly integrase strand transfer inhibitors, on early brain development, remains poorly understood. We used magnetic resonance imaging (MRI) to compare brain structure in children who are HIV-exposed and uninfected (CHEU) with prenatal dolutegravir (DTG) vs efavirenz (EFV) exposure.

methodsDolPHIN-2 was a randomized trial of pregnant women initiating DTG- vs EFV-based ART in the third trimester. At 3-4 years of age, a subgroup of their children from the South African cohort, along with HIV-unexposed (CHU) children, underwent T1-weighted MRI (DolPHIN-2 PLUS). Measurements of brain structure, including volume, cortical thickness, and surface area, were extracted using Freesurfer. Associations between ART /HIV exposure and child brain structure were examined using multiple linear regression.

resultsThis analysis included 58 children (25 CHEU [13 DTG, 12 EFV] and 33 CHU, mean age 46.35 months, 51.7% male). Demographic characteristics were similar across groups. Significant differences in global or regional brain volumes, cortical thickness, or surface area were not detected between DTG- and EFV-exposed children or between CHEU and CHU.

conclusionAmong this small sample of children at 3-4 years, statistically significant differences in global or regional brain structure were not detected between those exposed in the third trimester of pregnancy to DTG or EFV and CHU. Given the modest sample size, the study had limited power to detect small-to-moderate differences. Further longitudinal studies with larger sample sizes are needed to assess the effects of specific ART in the context of new regimens and better maternal HIV disease control on CHEU brain structure.

Indexed as

Anti-HIV AgentsBenzoxazinesBrainHeterocyclic Compounds, 3-RingHIV InfectionsPregnancy Complications, InfectiousPrenatal Exposure Delayed EffectsAdultAlkynesChild, PreschoolCyclopropanesDolutegravirFemaleHumansMagnetic Resonance ImagingMaleAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesDolutegravirefavirenzHeterocyclic Compounds, 3-RingOxazinesPiperazinesPyridonesART exposurechildrendolutegravirHIV exposureMRI

Identifiers

PMID41892690
PMCPMC13221953

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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.