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Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents

Human immunodeficiency virus (HIV) infection significantly affect neurodevelopmental and behavioral outcomes. We investigated whether alterations of gray matter organization and structural covariance networks with vertical HIV infection adolescents exist, by using the GAT toolbox. MRI data were anal...

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Autores principales: Li, Jielan, Gao, Lei, Wen, Zhi, Zhang, Jing, Wang, Panying, Tu, Ning, Lei, Hao, Lin, Fuchun, Gui, Xi’en, Wu, Guangyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775353/
https://www.ncbi.nlm.nih.gov/pubmed/29352127
http://dx.doi.org/10.1038/s41598-018-19290-5
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author Li, Jielan
Gao, Lei
Wen, Zhi
Zhang, Jing
Wang, Panying
Tu, Ning
Lei, Hao
Lin, Fuchun
Gui, Xi’en
Wu, Guangyao
author_facet Li, Jielan
Gao, Lei
Wen, Zhi
Zhang, Jing
Wang, Panying
Tu, Ning
Lei, Hao
Lin, Fuchun
Gui, Xi’en
Wu, Guangyao
author_sort Li, Jielan
collection PubMed
description Human immunodeficiency virus (HIV) infection significantly affect neurodevelopmental and behavioral outcomes. We investigated whether alterations of gray matter organization and structural covariance networks with vertical HIV infection adolescents exist, by using the GAT toolbox. MRI data were analysed from 25 HIV vertically infected adolescents and 33 HIV-exposed-uninfected control participants. The gray matter volume (GMV) was calculated, and structural brain networks were reconstructed from gray matter co-variance. Gray matter losses were pronounced in anterior cingulate cortex (ACC), right pallidum, right occipital lobe, inferior parietal lobe, and bilateral cerebellum crus. The global brain network measures were not significantly different between the groups; however, the nodal alterations were most pronounced in frontal, temporal, basal ganglia, cerebellum, and temporal lobes. Brain hubs in the HIV-infected subjects increased in number and tended to shift to sensorimotor and temporal areas. In the HIV-infected subjects, decreased GMVs in ACC and bilateral cerebellum were related to lower Mini-Mental State Examination scores; the CD4 counts were positively related to the GMVs in ACC and sensorimotor areas. These findings suggest that focally reduced gray matter, disrupted nodal profiles of structural wirings, and a shift in hub distribution may represent neuroanatomical biomarkers of HIV infection on the developing brain.
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spelling pubmed-57753532018-01-31 Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents Li, Jielan Gao, Lei Wen, Zhi Zhang, Jing Wang, Panying Tu, Ning Lei, Hao Lin, Fuchun Gui, Xi’en Wu, Guangyao Sci Rep Article Human immunodeficiency virus (HIV) infection significantly affect neurodevelopmental and behavioral outcomes. We investigated whether alterations of gray matter organization and structural covariance networks with vertical HIV infection adolescents exist, by using the GAT toolbox. MRI data were analysed from 25 HIV vertically infected adolescents and 33 HIV-exposed-uninfected control participants. The gray matter volume (GMV) was calculated, and structural brain networks were reconstructed from gray matter co-variance. Gray matter losses were pronounced in anterior cingulate cortex (ACC), right pallidum, right occipital lobe, inferior parietal lobe, and bilateral cerebellum crus. The global brain network measures were not significantly different between the groups; however, the nodal alterations were most pronounced in frontal, temporal, basal ganglia, cerebellum, and temporal lobes. Brain hubs in the HIV-infected subjects increased in number and tended to shift to sensorimotor and temporal areas. In the HIV-infected subjects, decreased GMVs in ACC and bilateral cerebellum were related to lower Mini-Mental State Examination scores; the CD4 counts were positively related to the GMVs in ACC and sensorimotor areas. These findings suggest that focally reduced gray matter, disrupted nodal profiles of structural wirings, and a shift in hub distribution may represent neuroanatomical biomarkers of HIV infection on the developing brain. Nature Publishing Group UK 2018-01-19 /pmc/articles/PMC5775353/ /pubmed/29352127 http://dx.doi.org/10.1038/s41598-018-19290-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Jielan
Gao, Lei
Wen, Zhi
Zhang, Jing
Wang, Panying
Tu, Ning
Lei, Hao
Lin, Fuchun
Gui, Xi’en
Wu, Guangyao
Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title_full Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title_fullStr Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title_full_unstemmed Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title_short Structural Covariance of Gray Matter Volume in HIV Vertically Infected Adolescents
title_sort structural covariance of gray matter volume in hiv vertically infected adolescents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775353/
https://www.ncbi.nlm.nih.gov/pubmed/29352127
http://dx.doi.org/10.1038/s41598-018-19290-5
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