Cargando…
Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study
BACKGROUND: Amputation in adults is a serious procedure or traumatic outcome, one that leads to a possible “remapping” of limb representations (somatotopy) in the motor and sensory cortex. The temporal and spatial extent underlying reorganization of somatotopy is unclear. The aim of this study was t...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088358/ https://www.ncbi.nlm.nih.gov/pubmed/33981337 http://dx.doi.org/10.1155/2021/8831379 |
_version_ | 1783686831533981696 |
---|---|
author | Bao, Bingbo Duan, Lei Wei, Haifeng Luo, Pengbo Zhu, Hongyi Gao, Tao Wei, Xiaoer Li, Jing Li, Yuehua Chai, Yimin Zhang, Changqing Zheng, Xianyou |
author_facet | Bao, Bingbo Duan, Lei Wei, Haifeng Luo, Pengbo Zhu, Hongyi Gao, Tao Wei, Xiaoer Li, Jing Li, Yuehua Chai, Yimin Zhang, Changqing Zheng, Xianyou |
author_sort | Bao, Bingbo |
collection | PubMed |
description | BACKGROUND: Amputation in adults is a serious procedure or traumatic outcome, one that leads to a possible “remapping” of limb representations (somatotopy) in the motor and sensory cortex. The temporal and spatial extent underlying reorganization of somatotopy is unclear. The aim of this study was to better understand how local and global structural plasticity in sensory-motor cortical networks changes temporally and spatially after upper-limb amputation. METHODS: We studied 8 healthy nonamputee control subjects and 16 complete upper-limb amputees. Resting-state MRI (rs-fMRI) was used to measure local and large-scale relative differences (compared to controls) in both the amplitude of low-frequency fluctuations (ALFF) and degree of centrality (DC) at 2 months, 6 months, and 12 months after traumatic amputation. RESULTS: In amputees, rs-fMRI scans revealed differences in spatial patterns of ALFF and DC among brain regions over time. Significant relative increases in ALFF and DC were detected not only in the sensory and motor cortex but also in related cortical regions believed to be involved in cognition and motor planning. We observed changes in the magnitude of ALFFs in the pre- and postcentral gyrus and primary sensory cortex, as well as in the anterior cingulate, parahippocampal gyrus, and hippocampus, 2 months after the amputation. The regional distribution of increases/decreases in ALFFs and DC documented at 2-month postamputation was very different from those at 6 and 12-month postamputation. CONCLUSION: Local and wide-spread changes in ALFFs in the sensorimotor cortex and cognitive-related brain regions after upper-limb amputation may imply dysfunction not only in sensory and motor function but also in areas responsible for sensorimotor integration and motor planning. These results suggest that cortical reorganization after upper extremity deafferentation is temporally and spatially more complicated than previously appreciated, affecting DC in widespread regions. |
format | Online Article Text |
id | pubmed-8088358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-80883582021-05-11 Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study Bao, Bingbo Duan, Lei Wei, Haifeng Luo, Pengbo Zhu, Hongyi Gao, Tao Wei, Xiaoer Li, Jing Li, Yuehua Chai, Yimin Zhang, Changqing Zheng, Xianyou Neural Plast Research Article BACKGROUND: Amputation in adults is a serious procedure or traumatic outcome, one that leads to a possible “remapping” of limb representations (somatotopy) in the motor and sensory cortex. The temporal and spatial extent underlying reorganization of somatotopy is unclear. The aim of this study was to better understand how local and global structural plasticity in sensory-motor cortical networks changes temporally and spatially after upper-limb amputation. METHODS: We studied 8 healthy nonamputee control subjects and 16 complete upper-limb amputees. Resting-state MRI (rs-fMRI) was used to measure local and large-scale relative differences (compared to controls) in both the amplitude of low-frequency fluctuations (ALFF) and degree of centrality (DC) at 2 months, 6 months, and 12 months after traumatic amputation. RESULTS: In amputees, rs-fMRI scans revealed differences in spatial patterns of ALFF and DC among brain regions over time. Significant relative increases in ALFF and DC were detected not only in the sensory and motor cortex but also in related cortical regions believed to be involved in cognition and motor planning. We observed changes in the magnitude of ALFFs in the pre- and postcentral gyrus and primary sensory cortex, as well as in the anterior cingulate, parahippocampal gyrus, and hippocampus, 2 months after the amputation. The regional distribution of increases/decreases in ALFFs and DC documented at 2-month postamputation was very different from those at 6 and 12-month postamputation. CONCLUSION: Local and wide-spread changes in ALFFs in the sensorimotor cortex and cognitive-related brain regions after upper-limb amputation may imply dysfunction not only in sensory and motor function but also in areas responsible for sensorimotor integration and motor planning. These results suggest that cortical reorganization after upper extremity deafferentation is temporally and spatially more complicated than previously appreciated, affecting DC in widespread regions. Hindawi 2021-04-23 /pmc/articles/PMC8088358/ /pubmed/33981337 http://dx.doi.org/10.1155/2021/8831379 Text en Copyright © 2021 Bingbo Bao et al. https://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 Bao, Bingbo Duan, Lei Wei, Haifeng Luo, Pengbo Zhu, Hongyi Gao, Tao Wei, Xiaoer Li, Jing Li, Yuehua Chai, Yimin Zhang, Changqing Zheng, Xianyou Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title | Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title_full | Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title_fullStr | Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title_full_unstemmed | Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title_short | Changes in Temporal and Spatial Patterns of Intrinsic Brain Activity and Functional Connectivity in Upper-Limb Amputees: An fMRI Study |
title_sort | changes in temporal and spatial patterns of intrinsic brain activity and functional connectivity in upper-limb amputees: an fmri study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088358/ https://www.ncbi.nlm.nih.gov/pubmed/33981337 http://dx.doi.org/10.1155/2021/8831379 |
work_keys_str_mv | AT baobingbo changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT duanlei changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT weihaifeng changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT luopengbo changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT zhuhongyi changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT gaotao changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT weixiaoer changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT lijing changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT liyuehua changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT chaiyimin changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT zhangchangqing changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy AT zhengxianyou changesintemporalandspatialpatternsofintrinsicbrainactivityandfunctionalconnectivityinupperlimbamputeesanfmristudy |