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Altered structural brain changes and neurocognitive performance in pediatric HIV
Pediatric HIV patients often suffer with neurodevelopmental delay and subsequently cognitive impairment. While tissue injury in cortical and subcortical regions in the brain of adult HIV patients has been well reported there is sparse knowledge about these changes in perinatally HIV infected pediatr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5304232/ https://www.ncbi.nlm.nih.gov/pubmed/28224079 http://dx.doi.org/10.1016/j.nicl.2017.01.032 |
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author | Yadav, Santosh K. Gupta, Rakesh K. Garg, Ravindra K. Venkatesh, Vimala Gupta, Pradeep K. Singh, Alok K. Hashem, Sheema Al-Sulaiti, Asma Kaura, Deepak Wang, Ena Marincola, Francesco M. Haris, Mohammad |
author_facet | Yadav, Santosh K. Gupta, Rakesh K. Garg, Ravindra K. Venkatesh, Vimala Gupta, Pradeep K. Singh, Alok K. Hashem, Sheema Al-Sulaiti, Asma Kaura, Deepak Wang, Ena Marincola, Francesco M. Haris, Mohammad |
author_sort | Yadav, Santosh K. |
collection | PubMed |
description | Pediatric HIV patients often suffer with neurodevelopmental delay and subsequently cognitive impairment. While tissue injury in cortical and subcortical regions in the brain of adult HIV patients has been well reported there is sparse knowledge about these changes in perinatally HIV infected pediatric patients. We analyzed cortical thickness, subcortical volume, structural connectivity, and neurocognitive functions in pediatric HIV patients and compared with those of pediatric healthy controls. With informed consent, 34 perinatally infected pediatric HIV patients and 32 age and gender matched pediatric healthy controls underwent neurocognitive assessment and brain magnetic resonance imaging (MRI) on a 3 T clinical scanner. Altered cortical thickness, subcortical volumes, and abnormal neuropsychological test scores were observed in pediatric HIV patients. The structural network connectivity analysis depicted lower connection strengths, lower clustering coefficients, and higher path length in pediatric HIV patients than healthy controls. The network betweenness and network hubs in cortico-limbic regions were distorted in pediatric HIV patients. The findings suggest that altered cortical and subcortical structures and regional brain connectivity in pediatric HIV patients may contribute to deficits in their neurocognitive functions. Further, longitudinal studies are required for better understanding of the effect of HIV pathogenesis on brain structural changes throughout the brain development process under standard ART treatment. |
format | Online Article Text |
id | pubmed-5304232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53042322017-02-21 Altered structural brain changes and neurocognitive performance in pediatric HIV Yadav, Santosh K. Gupta, Rakesh K. Garg, Ravindra K. Venkatesh, Vimala Gupta, Pradeep K. Singh, Alok K. Hashem, Sheema Al-Sulaiti, Asma Kaura, Deepak Wang, Ena Marincola, Francesco M. Haris, Mohammad Neuroimage Clin Regular Article Pediatric HIV patients often suffer with neurodevelopmental delay and subsequently cognitive impairment. While tissue injury in cortical and subcortical regions in the brain of adult HIV patients has been well reported there is sparse knowledge about these changes in perinatally HIV infected pediatric patients. We analyzed cortical thickness, subcortical volume, structural connectivity, and neurocognitive functions in pediatric HIV patients and compared with those of pediatric healthy controls. With informed consent, 34 perinatally infected pediatric HIV patients and 32 age and gender matched pediatric healthy controls underwent neurocognitive assessment and brain magnetic resonance imaging (MRI) on a 3 T clinical scanner. Altered cortical thickness, subcortical volumes, and abnormal neuropsychological test scores were observed in pediatric HIV patients. The structural network connectivity analysis depicted lower connection strengths, lower clustering coefficients, and higher path length in pediatric HIV patients than healthy controls. The network betweenness and network hubs in cortico-limbic regions were distorted in pediatric HIV patients. The findings suggest that altered cortical and subcortical structures and regional brain connectivity in pediatric HIV patients may contribute to deficits in their neurocognitive functions. Further, longitudinal studies are required for better understanding of the effect of HIV pathogenesis on brain structural changes throughout the brain development process under standard ART treatment. Elsevier 2017-02-02 /pmc/articles/PMC5304232/ /pubmed/28224079 http://dx.doi.org/10.1016/j.nicl.2017.01.032 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Yadav, Santosh K. Gupta, Rakesh K. Garg, Ravindra K. Venkatesh, Vimala Gupta, Pradeep K. Singh, Alok K. Hashem, Sheema Al-Sulaiti, Asma Kaura, Deepak Wang, Ena Marincola, Francesco M. Haris, Mohammad Altered structural brain changes and neurocognitive performance in pediatric HIV |
title | Altered structural brain changes and neurocognitive performance in pediatric HIV |
title_full | Altered structural brain changes and neurocognitive performance in pediatric HIV |
title_fullStr | Altered structural brain changes and neurocognitive performance in pediatric HIV |
title_full_unstemmed | Altered structural brain changes and neurocognitive performance in pediatric HIV |
title_short | Altered structural brain changes and neurocognitive performance in pediatric HIV |
title_sort | altered structural brain changes and neurocognitive performance in pediatric hiv |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5304232/ https://www.ncbi.nlm.nih.gov/pubmed/28224079 http://dx.doi.org/10.1016/j.nicl.2017.01.032 |
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