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Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity

People living with human immunodeficiency virus (PLWH) often have neurocognitive impairment. However, findings on HIV‐related differences in brain network function underlying these impairments are inconsistent. One principle frequently absent from these reports is that brain function is largely emer...

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Autores principales: Hall, Shana A., Bell, Ryan P., Davis, Simon W., Towe, Sheri L., Ikner, Taylor P., Meade, Christina S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449114/
https://www.ncbi.nlm.nih.gov/pubmed/34382273
http://dx.doi.org/10.1002/hbm.25592
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author Hall, Shana A.
Bell, Ryan P.
Davis, Simon W.
Towe, Sheri L.
Ikner, Taylor P.
Meade, Christina S.
author_facet Hall, Shana A.
Bell, Ryan P.
Davis, Simon W.
Towe, Sheri L.
Ikner, Taylor P.
Meade, Christina S.
author_sort Hall, Shana A.
collection PubMed
description People living with human immunodeficiency virus (PLWH) often have neurocognitive impairment. However, findings on HIV‐related differences in brain network function underlying these impairments are inconsistent. One principle frequently absent from these reports is that brain function is largely emergent from brain structure. PLWH commonly have degraded white matter; we hypothesized that functional communities connected by degraded white matter tracts would show abnormal functional connectivity. We measured white matter integrity in 69 PLWH and 67 controls using fractional anisotropy (FA) in 24 intracerebral white matter tracts. Then, among tracts with degraded FA, we identified gray matter regions connected to these tracts and measured their functional connectivity during rest. Finally, we identified cognitive impairment related to these structural and functional connectivity systems. We found HIV‐related decreased FA in the corpus callosum body (CCb), which coordinates activity between the left and right hemispheres, and corresponding increases in functional connectivity. Finally, we found that individuals with impaired cognitive functioning have lower CCb FA and higher CCb functional connectivity. This result clarifies the functional relevance of the corpus callosum in HIV and provides a framework in which abnormal brain function can be understood in the context of abnormal brain structure, which may both contribute to cognitive impairment.
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spelling pubmed-84491142021-09-24 Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity Hall, Shana A. Bell, Ryan P. Davis, Simon W. Towe, Sheri L. Ikner, Taylor P. Meade, Christina S. Hum Brain Mapp Research Articles People living with human immunodeficiency virus (PLWH) often have neurocognitive impairment. However, findings on HIV‐related differences in brain network function underlying these impairments are inconsistent. One principle frequently absent from these reports is that brain function is largely emergent from brain structure. PLWH commonly have degraded white matter; we hypothesized that functional communities connected by degraded white matter tracts would show abnormal functional connectivity. We measured white matter integrity in 69 PLWH and 67 controls using fractional anisotropy (FA) in 24 intracerebral white matter tracts. Then, among tracts with degraded FA, we identified gray matter regions connected to these tracts and measured their functional connectivity during rest. Finally, we identified cognitive impairment related to these structural and functional connectivity systems. We found HIV‐related decreased FA in the corpus callosum body (CCb), which coordinates activity between the left and right hemispheres, and corresponding increases in functional connectivity. Finally, we found that individuals with impaired cognitive functioning have lower CCb FA and higher CCb functional connectivity. This result clarifies the functional relevance of the corpus callosum in HIV and provides a framework in which abnormal brain function can be understood in the context of abnormal brain structure, which may both contribute to cognitive impairment. John Wiley & Sons, Inc. 2021-08-12 /pmc/articles/PMC8449114/ /pubmed/34382273 http://dx.doi.org/10.1002/hbm.25592 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Hall, Shana A.
Bell, Ryan P.
Davis, Simon W.
Towe, Sheri L.
Ikner, Taylor P.
Meade, Christina S.
Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title_full Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title_fullStr Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title_full_unstemmed Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title_short Human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
title_sort human immunodeficiency virus‐related decreases in corpus callosal integrity and corresponding increases in functional connectivity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449114/
https://www.ncbi.nlm.nih.gov/pubmed/34382273
http://dx.doi.org/10.1002/hbm.25592
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