Cortical structural changes related to early antiretroviral therapy (ART) interruption in perinatally HIV-infected children at 5 years of age.

ART interruption Brain morphometry Cortical thickness Gyrification Pediatric HIV

Journal

IBRO neuroscience reports
ISSN: 2667-2421
Titre abrégé: IBRO Neurosci Rep
Pays: Netherlands
ID NLM: 101775148

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 10 09 2020
accepted: 03 02 2021
entrez: 28 6 2021
pubmed: 29 6 2021
medline: 29 6 2021
Statut: epublish

Résumé

ART interruption in children can occur especially in resource-limited settings for reasons including poor adherence, stock-outs, ART intolerance of non-pediatric formulas and pill size, as well as ultimately to test for HIV remission. Although early ART initiation is now standard of care in pediatric HIV management, very little is known on the effect of early ART initiation or subsequent interruption on brain development. This study aimed to investigate the effect of ART interruption on brain cortical thickness (CT) and folding in a subset of children from the Children with HIV Early antiRetroviral therapy (CHER) trial cohort who all started ART before 18 months of age. CHER participants in the neuroimaging follow-up study had magnetic resonance (MRI) scans on a 3T Siemens Allegra brain scanner at age 5.44 ± 0.37 years. MR images were processed using the automated cross-sectional stream in FreeSurfer v6.0 and vertex wise comparisons of CT and local gyrification indices (LGIs) were performed between HIV+ children and HIV- controls, as well as between HIV+ children on interrupted or continuous ART and controls. HIV+ children (n = 46) showed thicker cortex than HIV- children (n = 29) in bilateral frontal and left temporo-insular regions but lower LGIs in left superior and bilateral medial orbitofrontal cortex extending into rostral anterior cingulate. Children on interrupted ART (n = 21) had thicker cortex than HIV- controls in left frontal and right insular regions, but children on continuous treatment (n = 25) showed no difference from controls. Children on both interrupted and continuous ART showed region-specific alterations in LGI relative to controls. Cortical folding appears more sensitive than CT to early life events including early ART and interruption. However, immune health resilience in children can translate to long term preservation of morphometric brain development, especially for those on early and continuous treatment.

Identifiants

pubmed: 34179869
doi: 10.1016/j.ibneur.2021.02.001
pii: S2667-2421(21)00010-5
pmc: PMC8211921
doi:

Types de publication

Journal Article

Langues

eng

Pagination

161-170

Subventions

Organisme : NICHD NIH HHS
ID : R01 HD071664
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH096559
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI053217
Pays : United States

Informations de copyright

© 2021 The Authors.

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Auteurs

Emmanuel C Nwosu (EC)

UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa.
Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, South Africa.

Martha J Holmes (MJ)

UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa.
Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, South Africa.

Mark F Cotton (MF)

Family Centre for Research with Ubuntu, Department of Paediatrics & Child Health, Tygerberg Children's Hospital and Faculty of Health Sciences, Stellenbosch University, Cape Town, South Africa.

Els Dobbels (E)

Family Centre for Research with Ubuntu, Department of Paediatrics & Child Health, Tygerberg Children's Hospital and Faculty of Health Sciences, Stellenbosch University, Cape Town, South Africa.

Francesca Little (F)

Department of Statistical Sciences, Faculty of Sciences, University of Cape Town, South Africa.

Barbara Laughton (B)

Family Centre for Research with Ubuntu, Department of Paediatrics & Child Health, Tygerberg Children's Hospital and Faculty of Health Sciences, Stellenbosch University, Cape Town, South Africa.

Andre van der Kouwe (A)

A.A. Martinos Centre for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA.
Department of Radiology, Harvard Medical School, Boston, MA, USA.

Ernesta M Meintjes (EM)

UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa.
Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, South Africa.

Frances Robertson (F)

UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa.
Neuroscience Institute, Faculty of Health Sciences, University of Cape Town, South Africa.

Classifications MeSH