The neurocognitive correlates of DTI indicators of white matter disorganization in pediatric moderate-to-severe traumatic brain injury.

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Frontiers in Human Neuroscience Pub Date : 2024-10-31 eCollection Date: 2024-01-01 DOI:10.3389/fnhum.2024.1470710
Daniel A Ignacio, Talin Babikian, Emily L Dennis, Kevin C Bickart, Meeryo Choe, Aliyah R Snyder, Anne Brown, Christopher C Giza, Robert F Asarnow
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引用次数: 0

Abstract

Introduction: Neuroimaging has expanded our understanding of pediatric brain disorders in which white matter organization and connectivity are crucial to functioning. Paralleling the known pathobiology of many neurodevelopmental disorders, traumatic brain injury (TBI) in childhood can alter trajectories of brain development. Specifically, diffusion tensor imaging (DTI) studies in TBI have demonstrated white matter (WM) abnormalities that suggest microstructural disruptions that may underlie atypical neurodevelopment. The neurocognitive correlates of these previous findings will be explored in this study.

Methods: Indicators of WM organization were collected in 44 pediatric patients with moderate/severe TBI and 76 controls over two post-injury time points: T1 (8-20 weeks) and T2 (54-96 weeks). Our previous work identified two TBI subgroups based on information processing differences: one with slower interhemispheric transfer times (IHTT) of visual information than controls and another with comparable IHTT. We extend this prior work by evaluating neurocognitive trajectories associated with divergent WM structure post-injury in slow and normal IHTT TBI subgroups.

Results: At T1, both TBI subgroups performed significantly worse than controls on a norm-referenced working memory index (WMI), but only the Normal IHTT TBI subgroup significantly improved over the 12-month follow-up period (p = 0.014) to match controls (p = 0.119). In contrast, the Slow IHTT TBI subgroup did not show any recovery in working memory performance over time and performed more poorly than the control group (p < 0.001) at T2. Improvement in one of the two WMI subtests was associated with DTI indicators of WM disorganization in CC tracts to the precentral, postcentral, frontal, and parietal cortices. IHTT and WM mean diffusivity predicted 79% of the variance in cognitive recovery from T1 to T2 when also accounting for other known predictors of TBI recovery.

Discussion: In the year following TBI, some pediatric patients experienced persisting working memory disturbance while others exhibited recovery; stratification was based on an event-related potential marker. More or less improvement in neurocognition was also associated with the degree of WM disorganization. IHTT, measured post-acutely after TBI, and progression of WM disorganization over time predicted neurocognitive trajectories at the chronic timeframe - potentially representing a prognostic biomarker.

小儿中重度脑外伤白质紊乱的 DTI 指标的神经认知相关性。
简介:神经影像学拓展了我们对小儿脑部疾病的认识,在这些疾病中,白质组织和连接性对功能起着至关重要的作用。与许多神经发育障碍的已知病理生物学相似,儿童时期的创伤性脑损伤(TBI)也会改变大脑的发育轨迹。具体而言,对创伤性脑损伤进行的弥散张量成像(DTI)研究显示,白质(WM)异常表明微观结构紊乱可能是非典型神经发育的基础。本研究将探讨这些先前发现的神经认知相关性:收集了 44 名中度/重度创伤性脑损伤儿科患者和 76 名对照组患者在伤后两个时间点的 WM 组织指标:T1(8-20周)和T2(54-96周)。我们之前的研究根据信息处理差异确定了两个创伤性脑损伤亚组:一个亚组的视觉信息半球间转移时间(IHTT)比对照组慢,另一个亚组的半球间转移时间与对照组相当。我们对这一研究成果进行了扩展,评估了与慢速和正常 IHTT TBI 亚群伤后 WM 结构差异相关的神经认知轨迹:在 T1 阶段,两个 TBI 亚组在常模参照工作记忆指数 (WMI) 上的表现均明显差于对照组,但只有正常 IHTT TBI 亚组在 12 个月的随访期间有明显改善(p = 0.014),达到了对照组的水平(p = 0.119)。相比之下,慢速 IHTT TBI 亚组的工作记忆表现没有随着时间的推移出现任何恢复,而且在 T2 阶段的表现比对照组更差(p < 0.001)。WMI 两项子测试中一项的改善与通往中枢前、中枢后、额叶和顶叶皮层的 CC 束中 WM 紊乱的 DTI 指标有关。在考虑到其他已知的 TBI 恢复预测因素的情况下,IHTT 和 WM 平均扩散率预测了从 T1 到 T2 认知恢复差异的 79%:讨论:在创伤性脑损伤后的一年中,一些儿科患者的工作记忆障碍持续存在,而另一些患者则表现出恢复;分层的依据是事件相关电位标记。神经认知能力的改善与否也与工作记忆紊乱的程度有关。在创伤性脑损伤急性期后测量的 IHTT 和 WM 紊乱程度随时间的推移可预测慢性期的神经认知轨迹,这可能是一种预后生物标志物。
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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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