TY - JOUR PY - 2017// TI - Diverging white matter trajectories in children after traumatic brain injury: the RAPBI study JO - Neurology A1 - Dennis, Emily L. A1 - Rashid, Faisal A1 - Ellis, Monica U. A1 - Babikian, Talin A1 - Vlasova, Roza M. A1 - Villalon-Reina, Julio E. A1 - Jin, Yan A1 - Olsen, Alexander A1 - Mink, Richard A1 - Babbitt, Christopher J. A1 - Johnson, Jeffrey A1 - Giza, Christopher C. A1 - Thompson, Paul M. A1 - Asarnow, Robert F. SP - 1392 EP - 1399 VL - 88 IS - 15 N2 - OBJECTIVE: To examine longitudinal trajectories of white matter organization in pediatric moderate/severe traumatic brain injury (msTBI) over a 12-month period.

METHODS: We studied 21 children (16 M/5 F) with msTBI, assessed 2-5 months postinjury and again 13-19 months postinjury, as well as 20 well-matched healthy control children. We assessed corpus callosum function through interhemispheric transfer time (IHTT), measured using event-related potentials, and related this to diffusion-weighted MRI measures of white matter (WM) microstructure. At the first time point, half of the patients with TBI had significantly slower IHTT (TBI-slow-IHTT, n = 11) and half were in the normal range (TBI-normal-IHTT, n = 10).

RESULTS: The TBI-normal-IHTT group did not differ significantly from healthy controls, either in WM organization in the chronic phase or in the longitudinal trajectory of WM organization between the 2 evaluations. In contrast, the WM organization of the TBI-slow-IHTT group was significantly lower than in healthy controls across a large portion of the WM. Longitudinal analyses showed that the TBI-slow-IHTT group experienced a progressive decline between the 2 evaluations in WM organization throughout the brain.

CONCLUSIONS: We present preliminary evidence suggesting a potential biomarker that identifies a subset of patients with impaired callosal organization in the first months postinjury who subsequently experience widespread continuing and progressive degeneration in the first year postinjury.

© 2017 American Academy of Neurology.

Language: en

LA - en SN - 0028-3878 UR - http://dx.doi.org/10.1212/WNL.0000000000003808 ID - ref1 ER -