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White Matter Abnormalities in Children with HIV Infection and Exposure

Background: Due to changes in guidelines and access to treatment, more children start combination antiretroviral therapy (ART) in infancy. With few studies examining the long-term effects of perinatal HIV infection and early ART on neurodevelopment, much is still unknown about brain maturation in th...

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Autores principales: Jankiewicz, Marcin, Holmes, Martha J., Taylor, Paul A., Cotton, Mark F., Laughton, Barbara, van der Kouwe, André J. W., Meintjes, Ernesta M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627060/
https://www.ncbi.nlm.nih.gov/pubmed/29033797
http://dx.doi.org/10.3389/fnana.2017.00088
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author Jankiewicz, Marcin
Holmes, Martha J.
Taylor, Paul A.
Cotton, Mark F.
Laughton, Barbara
van der Kouwe, André J. W.
Meintjes, Ernesta M.
author_facet Jankiewicz, Marcin
Holmes, Martha J.
Taylor, Paul A.
Cotton, Mark F.
Laughton, Barbara
van der Kouwe, André J. W.
Meintjes, Ernesta M.
author_sort Jankiewicz, Marcin
collection PubMed
description Background: Due to changes in guidelines and access to treatment, more children start combination antiretroviral therapy (ART) in infancy. With few studies examining the long-term effects of perinatal HIV infection and early ART on neurodevelopment, much is still unknown about brain maturation in the presence of HIV and ART. Follow-up studies of HIV infected (HIV+) children are important for monitoring brain development in the presence of HIV infection and ART. Methods: We use diffusion tensor imaging (DTI) to examine white matter (WM) in 65 HIV+ and 46 control (HIV exposed uninfected (HEU) and HIV unexposed uninfected (HU)) 7-year-old children. This is a follow up of a cohort studied at 5 years, where we previously reported lower fractional anisotropy (FA) in corticospinal tract (CST) and mean diffusivity (MD) increases in inferior/superior longitudinal fasciculi (ILF/SLF), inferior fronto-occipital fasciculus (IFOF) and uncinate fasciculus (UF) in HIV+ children compared to uninfected controls. In addition, we also found a difference in FA related to age at which ART was initiated. Results: At 7 years, we found two regions in the left IFOF and left ILF with lower FA in HIV+ children compared to controls. Higher MD was observed in a similar region in the IFOF, albeit bilaterally, as well as multiple clusters bilaterally in the superior corona radiata (SCR), the anterior thalamic radiation (ATR) and the right forceps minor. Unlike at 5 years, we found no impact on WM of ART initiation. In HEU children, we found a cluster in the right posterior corona radiata with higher FA compared to HU children, while bilateral regions in the CST demonstrated reduced MD. Conclusions: At age 7, despite early ART and viral load (VL) suppression, we continue to observe differences in WM integrity. WM damage observed at age 5 years persists, and new damage is evident. The continued observation of regions with lower FA and higher MD in HIV+ children point to disruptions in ongoing white matter development regardless of early ART. Lastly, in HEU children we find higher FA and lower MD in clusters in the CST tract suggesting that perinatal HIV/ART exposure has a long-term impact on WM development.
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spelling pubmed-56270602017-10-13 White Matter Abnormalities in Children with HIV Infection and Exposure Jankiewicz, Marcin Holmes, Martha J. Taylor, Paul A. Cotton, Mark F. Laughton, Barbara van der Kouwe, André J. W. Meintjes, Ernesta M. Front Neuroanat Neuroscience Background: Due to changes in guidelines and access to treatment, more children start combination antiretroviral therapy (ART) in infancy. With few studies examining the long-term effects of perinatal HIV infection and early ART on neurodevelopment, much is still unknown about brain maturation in the presence of HIV and ART. Follow-up studies of HIV infected (HIV+) children are important for monitoring brain development in the presence of HIV infection and ART. Methods: We use diffusion tensor imaging (DTI) to examine white matter (WM) in 65 HIV+ and 46 control (HIV exposed uninfected (HEU) and HIV unexposed uninfected (HU)) 7-year-old children. This is a follow up of a cohort studied at 5 years, where we previously reported lower fractional anisotropy (FA) in corticospinal tract (CST) and mean diffusivity (MD) increases in inferior/superior longitudinal fasciculi (ILF/SLF), inferior fronto-occipital fasciculus (IFOF) and uncinate fasciculus (UF) in HIV+ children compared to uninfected controls. In addition, we also found a difference in FA related to age at which ART was initiated. Results: At 7 years, we found two regions in the left IFOF and left ILF with lower FA in HIV+ children compared to controls. Higher MD was observed in a similar region in the IFOF, albeit bilaterally, as well as multiple clusters bilaterally in the superior corona radiata (SCR), the anterior thalamic radiation (ATR) and the right forceps minor. Unlike at 5 years, we found no impact on WM of ART initiation. In HEU children, we found a cluster in the right posterior corona radiata with higher FA compared to HU children, while bilateral regions in the CST demonstrated reduced MD. Conclusions: At age 7, despite early ART and viral load (VL) suppression, we continue to observe differences in WM integrity. WM damage observed at age 5 years persists, and new damage is evident. The continued observation of regions with lower FA and higher MD in HIV+ children point to disruptions in ongoing white matter development regardless of early ART. Lastly, in HEU children we find higher FA and lower MD in clusters in the CST tract suggesting that perinatal HIV/ART exposure has a long-term impact on WM development. Frontiers Media S.A. 2017-09-29 /pmc/articles/PMC5627060/ /pubmed/29033797 http://dx.doi.org/10.3389/fnana.2017.00088 Text en Copyright © 2017 Jankiewicz, Holmes, Taylor, Cotton, Laughton, van der Kouwe and Meintjes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Jankiewicz, Marcin
Holmes, Martha J.
Taylor, Paul A.
Cotton, Mark F.
Laughton, Barbara
van der Kouwe, André J. W.
Meintjes, Ernesta M.
White Matter Abnormalities in Children with HIV Infection and Exposure
title White Matter Abnormalities in Children with HIV Infection and Exposure
title_full White Matter Abnormalities in Children with HIV Infection and Exposure
title_fullStr White Matter Abnormalities in Children with HIV Infection and Exposure
title_full_unstemmed White Matter Abnormalities in Children with HIV Infection and Exposure
title_short White Matter Abnormalities in Children with HIV Infection and Exposure
title_sort white matter abnormalities in children with hiv infection and exposure
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627060/
https://www.ncbi.nlm.nih.gov/pubmed/29033797
http://dx.doi.org/10.3389/fnana.2017.00088
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