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A Longitudinal Study of White Matter Functional Network in Mild Traumatic Brain Injury

Authors :
Yulin Wang
Tianhui Li
Shuoqiu Gan
Xuebin Chang
Xuan Li
Shan Wang
Yinxiang Sun
Xuefei Yang
Xiaoyan Jia
Hao Yan
Debo Dong
Xuan Niu
Feng Xiong
Lijun Bai
Source :
Journal of neurotrauma 38(19), 2686-2697 (2021). doi:10.1089/neu.2021.0017
Publication Year :
2021
Publisher :
Mary Ann Liebert Inc, 2021.

Abstract

Some patients after mild traumatic brain injury (mTBI) experience microstructural damages in the long-distance white matter (WM) connections, which disrupts the functional connectome of large-scale brain networks that support cognitive function. Patterns of WM structural damage following mTBI were well documented using diffusion tensor imaging (DTI). However, the functional organization of WM and its association with gray matter functional networks (GM-FNs) and its DTI metrics remain unknown. The present study adopted resting-state functional magnetic resonance imaging to explore WM functional properties in mTBI patients (108 acute patients, 48 chronic patients, 46 healthy controls [HCs]). Eleven large-scale WM functional networks (WM-FNs) were constructed by the k-means clustering algorithm of voxel-wise WM functional connectivity (FC). Compared with HCs, acute mTBI patients observed enhanced FC between inferior fronto-occipital fasciculus (IFOF) WM-FN and primary sensorimotor WM-FNs, and cortical primary sensorimotor GM-FNs. Further, acute mTBI patients showed increased DTI metrics (mean diffusivity, axial diffusivity, and radial diffusivity) in deep WM-FNs and higher-order cognitive WM-FNs. Moreover, mTBI patients demonstrated full recovery of FC and partial recovery of DTI metrics in the chronic stage. Additionally, enhanced FC between IFOF WM-FN and anterior cerebellar GM-FN was correlated with impaired information processing speed. Our findings provide novel evidence for functional and structural alteration of WM-FNs in mTBI patients. Importantly, the convergent damage of the IFOF network might imply its crucial role in our understanding of the pathophysiology mechanism of mTBI patients.

Details

ISSN :
15579042 and 08977151
Volume :
38
Database :
OpenAIRE
Journal :
Journal of Neurotrauma
Accession number :
edsair.doi.dedup.....14ce1cae2aeeea6ea4afcefe3655fa00
Full Text :
https://doi.org/10.1089/neu.2021.0017