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  Vol. 65 No. 5, May 2008 TABLE OF CONTENTS
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Diffusion Tensor Tractography of Traumatic Diffuse Axonal Injury

Jun Yi Wang, MS; Khamid Bakhadirov, MD, MS; Michael D. Devous Sr, PhD; Hervé Abdi, PhD; Roddy McColl, PhD; Carol Moore, MA; Carlos D. Marquez de la Plata, PhD; Kan Ding, MD; Anthony Whittemore, MD, PhD; Evelyn Babcock, PhD; Tiffany Rickbeil, BS; Julia Dobervich, BS; David Kroll, BA; Bao Dao, BS; Nisha Mohindra, BS; Christopher J. Madden, MD; Ramon Diaz-Arrastia, MD, PhD

Arch Neurol. 2008;65(5):619-626.

Background  Diffuse axonal injury is a common consequence of traumatic brain injury that frequently involves the parasagittal white matter, corpus callosum, and brainstem.

Objective  To examine the potential of diffusion tensor tractography in detecting diffuse axonal injury at the acute stage of injury and predicting long-term functional outcome.

Design  Tract-derived fiber variables were analyzed to distinguish patients from control subjects and to determine their relationship to outcome.

Setting  Inpatient traumatic brain injury unit.

Patients  From 2005 to 2006, magnetic resonance images were acquired in 12 patients approximately 7 days after injury and in 12 age- and sex-matched controls.

Main Outcome Measures  Six fiber variables of the corpus callosum, fornix, and peduncular projections were obtained. Glasgow Outcome Scale–Extended scores were assessed approximately 9 months after injury in 11 of the 12 patients.

Results  At least 1 fiber variable of each region showed diffuse axonal injury–associated alterations. At least 1 fiber variable of the anterior body and splenium of the corpus callosum correlated significantly with the Glasgow Outcome Scale–Extended scores. The predicted outcome scores correlated significantly with actual scores in a mixed-effects model.

Conclusion  Diffusion tensor tractography–based quantitative analysis at the acute stage of injury has the potential to serve as a valuable biomarker of diffuse axonal injury and predict long-term outcome.


Author Affiliations: Department of Cognition and Neuroscience, The University of Texas at Dallas, Richardson (Ms Wang and Drs Bakhadirov and Abdi); and Departments of Radiology (Drs Devous, McColl, Whittemore, and Babcock, Messrs Kroll and Dao, and Ms Mohindra), Neurology (Mss Moore, Rickbeil, and Dobervich and Drs Marquez de la Plata, Ding, and Diaz-Arrastia), and Neurosurgery (Dr Madden), The University of Texas Southwestern Medical Center at Dallas.



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