OBJECTIVE: Our study addressed aims (1) to test the hypothesis that moderate-severe traumatic brain injury (TBI) in pediatric patients is associated with widespread white matter (WM) disruption, (2) to test the hypothesis that age and sex affect WM organization after injury, and (3) to examine associations between WM organization and neurobehavioral outcomes. METHODS: Data from 10 previously enrolled, existing cohorts recruited from local hospitals and clinics were shared with the Enhancing NeuroImaging Genetics Through Meta-Analysis (ENIGMA) Pediatric Moderate/Severe TBI (msTBI) working group. We conducted a coordinated analysis of diffusion MRI (dMRI) data using the ENIGMA dMRI processing pipeline. RESULTS: Five hundred seven children and adolescents (244 with complicated msTBI and 263 controls) were included. Patients were clustered into 3 postinjury intervals: acute/subacute, <2 months; postacute, 2 to 6 months; and chronic, â¥6 months. Outcomes were dMRI metrics and postinjury behavioral problems as indexed by the Child Behavior Checklist. Our analyses revealed altered WM diffusion metrics across multiple tracts and all postinjury intervals (effect sizes range d = -0.5 to -1.3). Injury severity is a significant contributor to the extent of WM alterations but explained less variance in dMRI measures with increasing time after injury. We observed a sex-by-group interaction: female patients with TBI had significantly lower fractional anisotropy in the uncinate fasciculus than controls (β = 0.043), which coincided with more parent-reported behavioral problems (β = -0.0027). CONCLUSIONS: WM disruption after msTBI is widespread, persistent, and influenced by demographic and clinical variables. Future work will test techniques for harmonizing neurocognitive data, enabling more advanced analyses to identify symptom clusters and clinically meaningful patient subtypes.
White Matter Disruption in Pediatric Traumatic Brain Injury: Results From ENIGMA Pediatric Moderate to Severe Traumatic Brain Injury.
阅读:5
作者:Dennis Emily L, Caeyenberghs Karen, Hoskinson Kristen R, Merkley Tricia L, Suskauer Stacy J, Asarnow Robert F, Babikian Talin, Bartnik-Olson Brenda, Bickart Kevin, Bigler Erin D, Ewing-Cobbs Linda, Figaji Anthony, Giza Christopher C, Goodrich-Hunsaker Naomi J, Hodges Cooper B, Hovenden Elizabeth S, Irimia Andrei, Königs Marsh, Levin Harvey S, Lindsey Hannah M, Max Jeffrey E, Newsome Mary R, Olsen Alexander, Ryan Nicholas P, Schmidt Adam T, Spruiell Matthew S, Wade Benjamin S C, Ware Ashley L, Watson Christopher G, Wheeler Anne L, Yeates Keith Owen, Zielinski Brandon A, Kochunov Peter, Jahanshad Neda, Thompson Paul M, Tate David F, Wilde Elisabeth A
| 期刊: | Neurology | 影响因子: | 8.500 |
| 时间: | 2021 | 起止号: | 2021 Jul 19; 97(3):e298-e309 |
| doi: | 10.1212/WNL.0000000000012222 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
