Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents

The CHER (Children with HIV Early Antiretroviral) trial found that early ART (12- weeks) reduced mortality and morbidity in children with perinatal HIV (CPHIV). Despite early ART, CPHIV from the CHER trial demonstrate neuroimaging alterations, but little is known about the effects of PHIV and long-...

Full description

Saved in:
Bibliographic Details
Main Author: Mac Arthur, Anika
Other Authors: Meintjes, Ernesta
Format: Thesis
Language:English
English
Published: Department of Human Biology 2025
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613927642234880
access_status_str Open Access
author Mac Arthur, Anika
author2 Meintjes, Ernesta
author_browse Mac Arthur, Anika
Meintjes, Ernesta
author_facet Meintjes, Ernesta
Mac Arthur, Anika
author_sort Mac Arthur, Anika
collection Thesis
description The CHER (Children with HIV Early Antiretroviral) trial found that early ART (12- weeks) reduced mortality and morbidity in children with perinatal HIV (CPHIV). Despite early ART, CPHIV from the CHER trial demonstrate neuroimaging alterations, but little is known about the effects of PHIV and long-term ART on the adolescent brain. Adolescence is a time of increased vulnerability to risk-taking behaviour. Here, neural circuits involved in reward processing during adolescence are investigated using functional MRI (fMRI). FMRI scans acquired during a Reward Magnitude Task were available for 106 socio economically matched adolescents (66 children perinatally infected with HIV (CPHIV), 40 controls living without HIV; age 150.4 years). Data were preprocessed using fMRIPrep. Differences in brain activation for anticipation, monetary wins vs losses, and reward/loss outcome magnitudes were compared between CPHIV and controls using FSL FEAT. Z-statistic images were thresholded at Z>3.1 and a cluster significance threshold of p=0.05. Across all subjects, there were robust responses to reward processing (win>loss) in the striatum (38,610mm3 ; peak MNI -10.1; 9.1; 0.7) and in the (ventromedial) prefrontal cortex (11,280mm3 ; peak MNI -5.3; 25.9; 41.5). There were no regions where activation increases, for any of our contrasts, were greater in CPHIV than controls, but CPHIV showed smaller activation increases than controls during anticipation and reward processing. We specifically saw smaller activation increases during processing of larger wins in 2 distinct small left superior frontal clusters as well as in the left paracingulate gyrus. Similar to findings from the Human Connectome Project in Development, the task reliably activated striatal and medial frontal regions involved in decision-making and reward seeking/processing. While we found no differences between CPHIV and controls within this reward processing network, CPHIV showed smaller activation differences in our contrasts in the left superior frontal cortex – a region involved in the working memory component of executive function. Notably, impaired working memory processing and storage, especially in the visual domain, has been reported previously in children living with HIV. The current finding suggests that HIV-related brain response abnormalities in working memory regions may impact reward processing.
format Thesis
id oai:open.uct.ac.za:11427/41030
institution University of Cape Town (South Africa)
language English
eng
last_indexed 2026-06-10T12:43:55.755Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2025
publishDateRange 2025
publishDateSort 2025
publisher Department of Human Biology
publisherStr Department of Human Biology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/41030 Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents Mac Arthur, Anika Meintjes, Ernesta Robertson, Frances HIV neural circuits adolescents The CHER (Children with HIV Early Antiretroviral) trial found that early ART (12- weeks) reduced mortality and morbidity in children with perinatal HIV (CPHIV). Despite early ART, CPHIV from the CHER trial demonstrate neuroimaging alterations, but little is known about the effects of PHIV and long-term ART on the adolescent brain. Adolescence is a time of increased vulnerability to risk-taking behaviour. Here, neural circuits involved in reward processing during adolescence are investigated using functional MRI (fMRI). FMRI scans acquired during a Reward Magnitude Task were available for 106 socio economically matched adolescents (66 children perinatally infected with HIV (CPHIV), 40 controls living without HIV; age 150.4 years). Data were preprocessed using fMRIPrep. Differences in brain activation for anticipation, monetary wins vs losses, and reward/loss outcome magnitudes were compared between CPHIV and controls using FSL FEAT. Z-statistic images were thresholded at Z>3.1 and a cluster significance threshold of p=0.05. Across all subjects, there were robust responses to reward processing (win>loss) in the striatum (38,610mm3 ; peak MNI -10.1; 9.1; 0.7) and in the (ventromedial) prefrontal cortex (11,280mm3 ; peak MNI -5.3; 25.9; 41.5). There were no regions where activation increases, for any of our contrasts, were greater in CPHIV than controls, but CPHIV showed smaller activation increases than controls during anticipation and reward processing. We specifically saw smaller activation increases during processing of larger wins in 2 distinct small left superior frontal clusters as well as in the left paracingulate gyrus. Similar to findings from the Human Connectome Project in Development, the task reliably activated striatal and medial frontal regions involved in decision-making and reward seeking/processing. While we found no differences between CPHIV and controls within this reward processing network, CPHIV showed smaller activation differences in our contrasts in the left superior frontal cortex – a region involved in the working memory component of executive function. Notably, impaired working memory processing and storage, especially in the visual domain, has been reported previously in children living with HIV. The current finding suggests that HIV-related brain response abnormalities in working memory regions may impact reward processing. 2025-02-26T11:38:59Z 2025-02-26T11:38:59Z 2024 2025-02-26T11:35:57Z Thesis / Dissertation Masters MSc http://hdl.handle.net/11427/41030 en eng application/pdf Department of Human Biology Faculty of Health Sciences University of Cape Town
spellingShingle HIV
neural circuits
adolescents
Mac Arthur, Anika
Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
thesis_degree_str Master's
title Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
title_full Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
title_fullStr Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
title_full_unstemmed Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
title_short Investigating the effects of living with HIV on neural circuits involved in reward processing in adolescents
title_sort investigating the effects of living with hiv on neural circuits involved in reward processing in adolescents
topic HIV
neural circuits
adolescents
url http://hdl.handle.net/11427/41030
work_keys_str_mv AT macarthuranika investigatingtheeffectsoflivingwithhivonneuralcircuitsinvolvedinrewardprocessinginadolescents