학술논문

White matter disruption in moderate/severe pediatric traumatic brain injury: Advanced tract-based analyses
Document Type
article
Source
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Childhood Injury
Biomedical Imaging
Rehabilitation
Traumatic Head and Spine Injury
Traumatic Brain Injury (TBI)
Behavioral and Social Science
Neurosciences
Unintentional Childhood Injury
Mind and Body
Pediatric
Clinical Research
Brain Disorders
Physical Injury - Accidents and Adverse Effects
Mental health
Adolescent
Brain
Brain Injuries
Child
Cognition Disorders
Cross-Sectional Studies
Diffusion Tensor Imaging
Female
Humans
Image Interpretation
Computer-Assisted
Longitudinal Studies
Male
White Matter
Young Adult
Diffusion tensor imaging
Traumatic brain injury
Longitudinal
Tractography
Biological psychology
Clinical and health psychology
Language
Abstract
Traumatic brain injury (TBI) is the leading cause of death and disability in children and can lead to a wide range of impairments. Brain imaging methods such as DTI (diffusion tensor imaging) are uniquely sensitive to the white matter (WM) damage that is common in TBI. However, higher-level analyses using tractography are complicated by the damage and decreased FA (fractional anisotropy) characteristic of TBI, which can result in premature tract endings. We used the newly developed autoMATE (automated multi-atlas tract extraction) method to identify differences in WM integrity. 63 pediatric patients aged 8-19 years with moderate/severe TBI were examined with cross sectional scanning at one or two time points after injury: a post-acute assessment 1-5 months post-injury and a chronic assessment 13-19 months post-injury. A battery of cognitive function tests was performed in the same time periods. 56 children were examined in the first phase, 28 TBI patients and 28 healthy controls. In the second phase 34 children were studied, 17 TBI patients and 17 controls (27 participants completed both post-acute and chronic phases). We did not find any significant group differences in the post-acute phase. Chronically, we found extensive group differences, mainly for mean and radial diffusivity (MD and RD). In the chronic phase, we found higher MD and RD across a wide range of WM. Additionally, we found correlations between these WM integrity measures and cognitive deficits. This suggests a distributed pattern of WM disruption that continues over the first year following a TBI in children.