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DESCRIPTION (provided by applicant): Moderate to severe non-penetrating pediatric traumatic brain injury (TBI) compromises distributed neural networks by disrupting axonal connections contributing to cognitive impairments. Cognitive functioning improves significantly over the first year post-TBI relative to the post-acute period in the vast majority of pediatric TBI survivors. There is evidence of restitution of neural connectivity over the first year post-TBI. The central hypothesis of this proposal is that cognitive deficits after non-penetrating pediatric TBI reflect white matter injury and disconnection, and that cognitive recovery occurs in conjunction with the restoration of neural network connectivity. Connectivity will be assessed using both structural brain imaging (MRI and DTI) and functional (electrophysiological, fMRI and neuropsychological) methods. We will study the structure and function of brain systems that are particularly vulnerable to white matter (WM) disruptions caused by TBI. The corpus callosum (CC) and a frontal-temporal-parietal (FTP) network that subserves spatial working memory will be studied as exemplars of neural networks disrupted by TBI. Innovative methods from behavioral neuroscience and neuroimaging will be used to assess the function of these networks, including separate measures of anterior and posterior CC function. Structural measures, including MRI and DTI, will be used to assess regional WM changes. The functional and structural measures will be administered longitudinally in 60 children with moderate/severe TBI and 60 age and gender matched controls. Children will be studied post-acutely (2-4 months post-TB I) and chronically (12 months post injury) to test the hypothesis that neurocognitive recovery following TBI is associated with increased WM connectivity and volume. This project will develop methods for studying brain/behavior relations in the CC following TBI that can be translated into experimental studies of small animals to help develop novel therapies. By explicating mechanisms that underlie naturally-occurring white matter injury and repair, the proposed project will identify potential new targets for interventions designed to accelerate the process of neurocognitive recovery.
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DOI: 10.1089/neu.2015.4012
发表时间: 2016-05-01
期刊: Journal of neurotrauma
影响因子: 4.2
作者: [Dennis EL, Hua X, Villalon-Reina J, Moran LM, Kernan C, Babikian T, Mink R, Babbitt C, Johnson J, Giza CC, Thompson PM, Asarnow RF]
通讯作者: Asarnow RF
The UCLA study of Predictors of Cognitive Functioning Following Moderate/Severe Pediatric Traumatic Brain Injury.
加州大学洛杉矶分校关于中度/重度小儿创伤性脑损伤后认知功能预测因素的研究。
DOI: 10.1017/s1355617716000175
发表时间: 2016
期刊: Journal of the International Neuropsychological Society : JINS
影响因子: --
作者: [Moran,LisaM, Babikian,Talin, DelPiero,Larissa, Ellis,MonicaU, Kernan,ClaudiaL, Newman,Nina, Giza,ChristopherC, Mink,Richard, Johnson,Jeffrey, Babbitt,Christopher, Asarnow,Robert]
通讯作者: Asarnow,Robert
Functional Brain Hyperactivations Are Linked to an Electrophysiological Measure of Slow Interhemispheric Transfer Time after Pediatric Moderate/Severe Traumatic Brain Injury.
功能性大脑过度激活与儿科中度/重度创伤性脑损伤后半球间传输时间缓慢的电生理学测量有关。
DOI: 10.1089/neu.2019.6532
发表时间: 2020
期刊: Journal of neurotrauma
影响因子: 4.2
作者: [Olsen,Alexander, Babikian,Talin, Dennis,EmilyL, Ellis-Blied,MonicaU, Giza,Christopher, Marion,SarahDeBoard, Mink,Richard, Johnson,Jeffrey, Babbitt,ChristopherJ, Thompson,PaulM, Asarnow,RobertF]
通讯作者: Asarnow,RobertF
CARE4Kids: Autonomic Biomarker Core
Augmentation of Cognitive Training in Children with TBI with D-Cycloserine
CORTICAL-STRIATAL DYSFUNCTION AND VULNERABILITY TO SCHIZOPHRENIA
Reconnection of Neural Networks and Cognitive Recovery after Pediatric TBI
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