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Neuroscience. 2023 Jun 1;520:46-57. doi: 10.1016/j.neuroscience.2023.03.029. Epub 2023 Apr 18.
2
White Matter Alterations Are Associated With Cognitive Dysfunction Decades After Moderate-to-Severe Traumatic Brain Injury and/or Posttraumatic Stress Disorder.脑白质改变与中重度创伤性脑损伤和/或创伤后应激障碍数十年后认知功能障碍有关。
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本文引用的文献

1
White Matter Alterations Are Associated With Cognitive Dysfunction Decades After Moderate-to-Severe Traumatic Brain Injury and/or Posttraumatic Stress Disorder.脑白质改变与中重度创伤性脑损伤和/或创伤后应激障碍数十年后认知功能障碍有关。
Biol Psychiatry Cogn Neurosci Neuroimaging. 2021 Nov;6(11):1100-1109. doi: 10.1016/j.bpsc.2021.04.014. Epub 2021 May 4.
2
The Prevalence and Stability of Sleep-Wake Disturbance and Fatigue throughout the First Year after Mild Traumatic Brain Injury.轻度创伤性脑损伤后一年中睡眠-觉醒障碍和疲劳的发生率和稳定性。
J Neurotrauma. 2020 Dec 1;37(23):2528-2541. doi: 10.1089/neu.2019.6898. Epub 2020 Jul 8.
3
Evaluating spatiotemporal microstructural alterations following diffuse traumatic brain injury.评估弥漫性创伤性脑损伤后的时空微观结构改变。
Neuroimage Clin. 2020;25:102136. doi: 10.1016/j.nicl.2019.102136. Epub 2019 Dec 14.
4
Interactive effect of age and APOE-ε4 allele load on white matter myelin content in cognitively normal middle-aged subjects.认知正常的中年受试者中年龄和 APOE-ε4 等位基因负荷对白质髓鞘含量的交互作用。
Neuroimage Clin. 2019;24:101983. doi: 10.1016/j.nicl.2019.101983. Epub 2019 Aug 16.
5
Post-Traumatic Stress Disorder after Civilian Traumatic Brain Injury: A Systematic Review and Meta-Analysis of Prevalence Rates.创伤性脑损伤后创伤后应激障碍:患病率的系统评价和荟萃分析。
J Neurotrauma. 2019 Dec 1;36(23):3220-3232. doi: 10.1089/neu.2018.5759. Epub 2019 Aug 2.
6
Whole-brain white matter organization, intelligence, and educational attainment.全脑白质结构、智力与教育成就。
Trends Neurosci Educ. 2019 Jun;15:38-47. doi: 10.1016/j.tine.2019.02.004. Epub 2019 Mar 2.
7
Traumatic brain injury: neuropathological, neurocognitive and neurobehavioral sequelae.创伤性脑损伤:神经病理学、神经认知和神经行为后遗症。
Pituitary. 2019 Jun;22(3):270-282. doi: 10.1007/s11102-019-00957-9.
8
Descriptive statistics and normality tests for statistical data.统计数据的描述性统计和正态性检验。
Ann Card Anaesth. 2019 Jan-Mar;22(1):67-72. doi: 10.4103/aca.ACA_157_18.
9
Tauopathy in veterans with long-term posttraumatic stress disorder and traumatic brain injury.创伤后应激障碍和创伤性脑损伤老兵的 tau 病。
Eur J Nucl Med Mol Imaging. 2019 May;46(5):1139-1151. doi: 10.1007/s00259-018-4241-7. Epub 2019 Jan 7.
10
Amyloid pathology fingerprint differentiates post-traumatic stress disorder and traumatic brain injury.淀粉样蛋白病理特征可区分创伤后应激障碍和创伤性脑损伤。
Neuroimage Clin. 2018 Jun 5;19:716-726. doi: 10.1016/j.nicl.2018.05.016. eCollection 2018.

自我报告的疲劳与长期创伤性脑损伤和创伤后应激障碍患者的白质改变有关。

Self-reported Fatigue was Associated with Increased White-matter Alterations in Long-term Traumatic Brain Injury and Posttraumatic Stress Disorder Patients.

机构信息

Thompson Institute, University of the Sunshine Coast, Sunshine Coast, QLD 4575, Australia.

Thompson Institute, University of the Sunshine Coast, Sunshine Coast, QLD 4575, Australia.

出版信息

Neuroscience. 2023 Jun 1;520:46-57. doi: 10.1016/j.neuroscience.2023.03.029. Epub 2023 Apr 18.

DOI:10.1016/j.neuroscience.2023.03.029
PMID:37080447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10357124/
Abstract

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%, P = 0.06), and significantly higher in both TBI + PTSD (66.67%, P = 0.001) and PTSD groups (79.25%, P < 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 (P ≤ 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.

摘要

疲劳是创伤性脑损伤 (TBI) 和创伤后应激障碍 (PTSD) 的长期问题,针对 TBI 和/或 PTSD 队列中与疲劳相关的白质变化的研究有限。这项探索性横断面研究使用弥散张量成像 (DTI) 和神经心理学数据,这些数据来自 153 名男性越南战争退伍军人,作为阿尔茨海默病神经影像学倡议-国防部的一部分,临床上分为对照组退伍军人、PTSD、TBI 和 TBI 和 PTSD 均有的退伍军人 (TBI + PTSD)。疲劳的存在通过以下问题来定义:“白天你是否经常感到疲倦、疲劳或困倦?”。在每个临床组中,使用基于束的空间统计学体素差异,比较疲劳和非疲劳亚组之间的 DTI 数据差异。在对照组中报告了疲劳(29.55%),TBI 中略高(52.17%,P = 0.06),TBI + PTSD 和 PTSD 组中均显著升高(66.67%,P = 0.001 和 79.25%,P < 0.001)。与非疲劳亚组相比,在对照组或 TBI 的疲劳亚组中未观察到白质差异,而疲劳 PTSD 亚组仅显示出扩散测量值(即径向和轴向)增加,而疲劳 TBI + PTSD 亚组显示出分数各向异性降低和扩散测量值增加(P ≤ 0.05)。这些结果初步表明,TBI + PTSD 和 PTSD 数十年后创伤后疲劳的报告显著增加,并且可能与 PTSD 和 TBI + PTSD 中的白质微观结构差异有关。需要更大队列和详细疲劳评估的未来研究来确定这些队列中与疲劳相关的白质变化。