Cargando…

Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents

Although evidence from studies on blind adults indicates that visual deprivation early in life leads to structural and functional disruption and reorganization of the brain, whether young blind people show similar patterns remains unknown. Therefore, this study is aimed at exploring the structural a...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Zhifeng, Xu, Jinping, Shi, Leilei, Liu, Xia, Hou, Fen, Zhou, Jingyi, Luo, Jinpei, Hu, Qingmao, Li, Hengguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408999/
https://www.ncbi.nlm.nih.gov/pubmed/30996726
http://dx.doi.org/10.1155/2019/2747460
_version_ 1783401889241497600
author Zhou, Zhifeng
Xu, Jinping
Shi, Leilei
Liu, Xia
Hou, Fen
Zhou, Jingyi
Luo, Jinpei
Hu, Qingmao
Li, Hengguo
author_facet Zhou, Zhifeng
Xu, Jinping
Shi, Leilei
Liu, Xia
Hou, Fen
Zhou, Jingyi
Luo, Jinpei
Hu, Qingmao
Li, Hengguo
author_sort Zhou, Zhifeng
collection PubMed
description Although evidence from studies on blind adults indicates that visual deprivation early in life leads to structural and functional disruption and reorganization of the brain, whether young blind people show similar patterns remains unknown. Therefore, this study is aimed at exploring the structural and functional alterations of the brain of early-blind adolescents (EBAs) compared to normal-sighted controls (NSCs) and investigating the effects of residual light perception on brain microstructure and function in EBAs. We obtained magnetic resonance imaging (MRI) data from 23 EBAs (8 with residual light perception (LPs), 15 without light perception (NLPs)) and 21 NSCs (age range 11-19 years old). Whole-brain voxel-based analyses of diffusion tensor imaging metrics and region-of-interest analyses of resting-state functional connectivity (RSFC) were performed to compare patterns of brain microstructure and the corresponding RSFC between the groups. The results showed that structural disruptions of LPs and NLPs were mainly located in the occipital visual pathway. Compared with NLPs, LPs showed increased fractional anisotropy (FA) in the superior frontal gyrus and reduced diffusivity in the caudate nucleus. Moreover, the correlations between FA of the occipital cortices or mean diffusivity of the lingual gyrus and age were consistent with the development trajectory of the brain in NSCs, but inconsistent or even opposite in EBAs. Additionally, we found functional, but not structural, reorganization in NLPs compared with NSCs, suggesting that functional neuroplasticity occurs earlier than structural neuroplasticity in EBAs. Altogether, these findings provided new insights into the mechanisms underlying the neural reorganization of the brain in adolescents with early visual deprivation.
format Online
Article
Text
id pubmed-6408999
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-64089992019-04-17 Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents Zhou, Zhifeng Xu, Jinping Shi, Leilei Liu, Xia Hou, Fen Zhou, Jingyi Luo, Jinpei Hu, Qingmao Li, Hengguo Neural Plast Research Article Although evidence from studies on blind adults indicates that visual deprivation early in life leads to structural and functional disruption and reorganization of the brain, whether young blind people show similar patterns remains unknown. Therefore, this study is aimed at exploring the structural and functional alterations of the brain of early-blind adolescents (EBAs) compared to normal-sighted controls (NSCs) and investigating the effects of residual light perception on brain microstructure and function in EBAs. We obtained magnetic resonance imaging (MRI) data from 23 EBAs (8 with residual light perception (LPs), 15 without light perception (NLPs)) and 21 NSCs (age range 11-19 years old). Whole-brain voxel-based analyses of diffusion tensor imaging metrics and region-of-interest analyses of resting-state functional connectivity (RSFC) were performed to compare patterns of brain microstructure and the corresponding RSFC between the groups. The results showed that structural disruptions of LPs and NLPs were mainly located in the occipital visual pathway. Compared with NLPs, LPs showed increased fractional anisotropy (FA) in the superior frontal gyrus and reduced diffusivity in the caudate nucleus. Moreover, the correlations between FA of the occipital cortices or mean diffusivity of the lingual gyrus and age were consistent with the development trajectory of the brain in NSCs, but inconsistent or even opposite in EBAs. Additionally, we found functional, but not structural, reorganization in NLPs compared with NSCs, suggesting that functional neuroplasticity occurs earlier than structural neuroplasticity in EBAs. Altogether, these findings provided new insights into the mechanisms underlying the neural reorganization of the brain in adolescents with early visual deprivation. Hindawi 2019-02-24 /pmc/articles/PMC6408999/ /pubmed/30996726 http://dx.doi.org/10.1155/2019/2747460 Text en Copyright © 2019 Zhifeng Zhou et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhou, Zhifeng
Xu, Jinping
Shi, Leilei
Liu, Xia
Hou, Fen
Zhou, Jingyi
Luo, Jinpei
Hu, Qingmao
Li, Hengguo
Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title_full Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title_fullStr Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title_full_unstemmed Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title_short Alterations of the Brain Microstructure and Corresponding Functional Connectivity in Early-Blind Adolescents
title_sort alterations of the brain microstructure and corresponding functional connectivity in early-blind adolescents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408999/
https://www.ncbi.nlm.nih.gov/pubmed/30996726
http://dx.doi.org/10.1155/2019/2747460
work_keys_str_mv AT zhouzhifeng alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT xujinping alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT shileilei alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT liuxia alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT houfen alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT zhoujingyi alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT luojinpei alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT huqingmao alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents
AT lihengguo alterationsofthebrainmicrostructureandcorrespondingfunctionalconnectivityinearlyblindadolescents