4.5 Article

Serial Changes in the White Matter Diffusion Tensor Imaging Metrics in Moderate Traumatic Brain Injury and Correlation with Neuro-Cognitive Function

Journal

JOURNAL OF NEUROTRAUMA
Volume 26, Issue 4, Pages 481-495

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2008.0461

Keywords

diffuse axonal injury; diffusion tensor imaging; fractional anisotropy; neuropsychological test; traumatic brain injury; white matter

Funding

  1. Indian Council of Medical Research [5/4-5/13/Neuro/2004-NCD-1]
  2. Indian Council of Medical Research, New Delhi, India
  3. University Grant Commission, New Delhi, India

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Diffuse axonal injury (DAI) that follows traumatic brain injury (TBI) is thought to be a major contributor to neurocognitive dysfunction that sometimes follows TBI. Conventional magnetic resonance imaging (MRI), diffusion tensor imaging (DTI) and neuropsychological tests (NPT) were performed on 38 TBI patients [hemorrhagic DAI (H-DAI, n = 8), non-hemorrhagic (Nh-DAI, n = 7), with no apparent DAI on conventional MRI (NA-DAI, n 23)] with a Glasgow Coma Scale score ranging between 9 and 13. The fractional anisotropy (FA) and mean diffusivity (MD) were quantified from different regions of the corpus callosum (CC), and peri-ventricular white matter (PWM) within 5-14 days and 6 months following TBI. Patients in all three groups showed decreased FA in the anterior limb of the internal capsule (ALIC) and the posterior limb of the internal capsule ( PLIC), while the genu of the CC showed a decrease in the H-DAI group during the early period following TBI that persisted 6 months later, which appeared to be consistent with axonopathy. In patients without abnormalities on conventional MRI and DTI in the initial phase, a significant decrease in FA and increase in MD were observed in a few regions of the CC at 6 months, which was suggestive of demyelination/gliosis. The changes in FA and MD in the CC and PWM at 6 months follow-up showed significant correlation with some of the NPT performed in the three groups. DTI demonstrates axonopathy in the acute stage, as well as at secondary stages, at 6 months post-injury in the CC and PWM in regions of normal-appearing white matter on conventional MRI.

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