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Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury.

Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Research Abstract Details 

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  • Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Abstract Text:

    elisabeth a wildeElisabeth A Wilde,erin d biglerErin D Bigler,janelle m haiderJanelle M Haider,zili chuZili Chu,harvey s levinHarvey S Levin,xiaoqi liXiaoqi Li,jill v hunterJill V Hunter,

    In relation to the adult brain, the immature brain might be more vulnerable to damage during and following traumatic brain injury, particularly in white-matter tracts. Given well-established evidence of corpus callosum atrophy, we hypothesized that anterior commissure volume (using quantitative magnetic resonance imaging [MRI]) in this structure would be decreased in children with moderate to severe traumatic brain injury relative to typically developing children. Second, given the purported role of the anterior commissure in interhemispheric axon conveyance between temporal lobes, we hypothesized that temporal lobe white matter, temporal lesion volume, and injury severity (Glasgow Coma Scale score) would be predictive of decreased anterior commissure cross-sectional volume in patients with traumatic brain injury. Finally, we wished to establish the relationship between the anterior commissure and the temporal stem, a major white-matter tract into the temporal lobes, using diffusion tensor imaging fiber-tracking maps for each patient. We also hypothesized that children with traumatic brain injury would exhibit decreased fractional anisotropy in relation to typically developing children in a fiber system including the anterior commissure and the temporal lobes. Decreased anterior commissure cross-sectional volume was observed in patients with traumatic brain injury, and, as predicted, anterior commissure and temporal white-matter volumes were positively related to each other and to higher Glasgow Coma Scale scores. Lesion volume was not independently predictive of anterior commissure volume in the overall model. Diffusion tensor imaging fractional anisotropy values differed between the groups for the temporal stem-anterior commissure system, with the traumatic brain injury group exhibiting decreased fractional anisotropy. The anterior commissure, like the corpus callosum, appears to be highly vulnerable to white-matter degenerative changes resulting from mechanisms such as the direct impact of trauma, progressive axonal injury as tissue in other brain regions atrophies, or myelin degeneration. This is the first systematic examination of anterior commissure atrophy following traumatic brain injury using in vivo quantitative MRI and diffusion tensor imaging fiber tracking in pediatric subjects.

    Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Publishing Authors By Initials

    ea wildeEA Wilde,ed biglerED Bigler,jm haiderJM Haider,z chuZ Chu,hs levinHS Levin,x liX Li,jv hunterJV Hunter,

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    Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of child neurology

    VOLUME: 21

    Page Numbers: 769-76

    Journal Abbreviation:

    ISSN: 0883-0738

    DAY: 3

    MONTH: Sep

    YEAR: 2006

    Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Information

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    LANGUAGE: eng

    NlmUniqueID: 8606714

    Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. Keywords Mesh Terms:

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    Grant and Affiliation Information for Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury.

    AFFILIATION: Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, 1709 Dryden Road, Houston, TX 77030, USA.

    Country: Canada

    Canada Research PublicationCanada Research Publication

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    MEDLINETA: J Child Neurol

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