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Diffusion tensor imaging differences relate to memory deficits in diffuse traumatic brain injury.
- Source :
-
BMC neurology [BMC Neurol] 2011 Feb 23; Vol. 11, pp. 24. Date of Electronic Publication: 2011 Feb 23. - Publication Year :
- 2011
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Abstract
- Background: Memory is one of the most impaired functions after traumatic brain injury (TBI). We used diffusion tensor imaging (DTI) to determine the structural basis of memory deficit. We correlated fractional anisotropy (FA) of the fasciculi connecting the main cerebral regions that are involved in declarative and working memory functions.<br />Methods: Fifteen patients with severe and diffuse TBI and sixteen healthy controls matched by age and years of education were scanned. The neuropsychological assessment included: Letter-number sequencing test (LNS), 2-back task, digit span (forwards and backwards) and the Rivermead profilet. DTI was analyzed by a tract-based spatial statics (TBSS) approach.<br />Results: Whole brain DTI analysis showed a global decrease in FA values that correlated with the 2-back d-prime index, but not with the Rivermead profile. ROI analysis revealed positive correlations between working memory performance assessed by 2-back d-prime and superior longitudinal fasciculi, corpus callosum, arcuate fasciculi and fornix. Declarative memory assessed by the Rivermead profile scores correlated with the fornix and the corpus callosum.<br />Conclusions: Diffuse TBI is associated with a general decrease of white matter integrity. Nevertheless deficits in specific memory domains are related to different patterns of white matter damage.
- Subjects :
- Adolescent
Adult
Anisotropy
Brain Injuries complications
Brain Mapping methods
Cross-Sectional Studies
Female
Humans
Male
Memory Disorders complications
Neuropsychological Tests
Brain Injuries pathology
Brain Injuries psychology
Diffusion Tensor Imaging methods
Memory Disorders pathology
Nerve Fibers, Myelinated pathology
Neural Pathways pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1471-2377
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- BMC neurology
- Publication Type :
- Academic Journal
- Accession number :
- 21345223
- Full Text :
- https://doi.org/10.1186/1471-2377-11-24