Bidirectional Changes in Anisotropy Are Associated with Outcomes in Mild Traumatic Brain Injury. Academic Article uri icon

Overview

abstract

  • BACKGROUND AND PURPOSE: Mild traumatic brain injury results in a heterogeneous constellation of deficits and symptoms that persist in a subset of patients. This prospective longitudinal study identifies early diffusion tensor imaging biomarkers of mild traumatic brain injury that significantly relate to outcomes at 1 year following injury. MATERIALS AND METHODS: DTI was performed on 39 subjects with mild traumatic brain injury within 16 days of injury and 40 controls; 26 subjects with mild traumatic brain injury returned for follow-up at 1 year. We identified subject-specific regions of abnormally high and low fractional anisotropy and calculated mean fractional anisotropy, axial diffusivity, radial diffusivity, and mean diffusivity across all white matter voxels brain-wide and each of several white matter regions. Assessment of cognitive performance and symptom burden was performed at 1 year. RESULTS: Significant associations of brain-wide DTI measures and outcomes included the following: mean radial diffusivity and mean diffusivity with memory; and mean fractional anisotropy, radial diffusivity, and mean diffusivity with health-related quality of life. Significant differences in outcomes were found between subjects with and without abnormally high fractional anisotropy for the following white matter regions and outcome measures: left frontal lobe and left temporal lobe with attention at 1 year, left and right cerebelli with somatic postconcussion symptoms at 1 year, and right thalamus with emotional postconcussion symptoms at 1 year. CONCLUSIONS: Individualized assessment of DTI abnormalities significantly relates to long-term outcomes in mild traumatic brain injury. Abnormally high fractional anisotropy is significantly associated with better outcomes and might represent an imaging correlate of postinjury compensatory processes.

authors

  • Strauss, Sara
  • Kim, N
  • Branch, C A
  • Kahn, M E
  • Kim, M
  • Lipton, R B
  • Provataris, J M
  • Scholl, H F
  • Zimmerman, M E
  • Lipton, M L

publication date

  • June 9, 2016

Identity

PubMed Central ID

  • PMC5148740

Scopus Document Identifier

  • 84995699224

Digital Object Identifier (DOI)

  • 10.3174/ajnr.A4851

PubMed ID

  • 27282864

Additional Document Info

volume

  • 37

issue

  • 11