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Self-reported fatigue was associated with increased white-matter alterations in long-term traumatic brain injury and posttraumatic stress disorder patients
Journal article   Peer reviewed

Self-reported fatigue was associated with increased white-matter alterations in long-term traumatic brain injury and posttraumatic stress disorder patients

Abdalla Z Mohamed, Jim Lagopoulos, Fatima A Nasrallah, Zack Shan and Department of Defense Alzheimer's Disease Neuroimaging Initiative
Neuroscience, Vol.520, pp.46-57
2023
PMCID: PMC10357124
PMID: 37080447
Appears in  Thompson Institute Research Collection
url
https://doi.org/10.1016/j.neuroscience.2023.03.029View
Published Version

Abstract

Diffusion Tensor Imaging (DTI) Fatigue Posttraumatic Stress Disorder Tract Based Spatial Statistics (TBSS) Traumatic brain Injury Stress related disorders trauma Neuroimaging Thompson Institute Special Collection UniSC Diversity Area - Disability and Inclusion
Fatigue is a long-lasting problem in traumatic brain injury (TBI) and post-traumatic stress disorder (PTSD), with limited research that investigated the fatigue-related white-matter changes within TBI and/or PTSD cohorts. This exploratory cross-sectional study used diffusion tensor imaging (DTI) and neuropsychological data collected from 153 male Vietnam War veterans, as part of the Alzheimer’s Disease Neuroimaging Initiative - Department of Defense, and were divided clinically into control veterans, PTSD, TBI, and with both TBI and PTSD (TBI + PTSD). The existence of fatigue was defined by the question “Do you often feel tired, fatigued, or sleepy during the daytime?”. DTI data were compared between fatigue and non-fatigue subgroups in each clinical group using tract-based spatial statistics voxel-based differences. Fatigue was reported in controls (29.55%), slightly higher in TBI (52.17%, PBenf = 0.06), and significantly higher in both TBI + PTSD (66.67%, PBenf = 0.001) and PTSD groups (79.25%, PBenf < 0.001). Compared to non-fatigued subgroups, no white-matter differences were observed in the fatigued subgroups of control or TBI, while the fatigued PTSD subgroup only showed increased diffusivity measures (i.e., radial and axial), and the fatigued TBI + PTSD subgroup showed decreased fractional anisotropy and increased diffusivity measures (PFWE ≤ 0.05). The results act as preliminary findings suggesting fatigue to be significantly reported in TBI + PTSD and PTSD decades post-trauma with a possible link to white-matter microstructural differences in both PTSD and TBI + PTSD. Future studies with larger cohorts and detailed fatigue assessments would be required to identify the white-matter changes associated with fatigue in these cohorts.

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