Diffusion Tensor Imaging of Wallerian Degeneration in MS
Project Number5R01NS052505-02
Contact PI/Project LeaderHASAN, KHADER M
Awardee OrganizationUNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
Description
Abstract Text
DESCRIPTION (provided by applicant): Diffusion tensor MRI (DTI) is a powerful in vivo technique that is sensitive to deep brain tissue water microdynamics and microstructure. DTI-derived orientation and scalar maps have the unique potential to provide objective and specific measures of the Multiple Sclerosis pathology. The hallmarks of MS pathology may include inflammation, demyelination, gliosis, direct axonal loss directly or indirectly through Wallerian degeneration (WD). WD can cause axonal loss distal from the initial demyelinating lesion and its signature in MS has not been elucidated using a comprehensive DTI and conventional MRI approach. The Corpus callosum (CC), pyramidal, corticospinal tracts coursing through the internal capsule (IC) are important structures that are implicated in neurological deficit in MS. Unfortunately, the limited published literature on DTI of MS in these structures is often inconsistent and sometimes contradictory. Based on our preliminary studies, these inconsistencies and contradictions, at least in part, could be attributed to sub-optimal acquisition schemes, arbitrary region of interest placement, failure to recognize the regional heterogeneity of these structures, the age and gender dependence of DTI measure. In order to overcome some of these limitations, we propose to acquire DTI data at 3.0 T using parallel imaging at different age groups on normal males and females. In addition, MRI data will also be acquired on MS subjects. The DTI data will be acquired from the whole brain using optimized Icosa21 scheme that is shown to be balanced and unbiased. Specifically we will concentrate on the CC, pyramidal and CST tracts which are implicated in MS, to identify WD signature in MS. We will divide the corpus callosum into seven functionally distinct sub regions. Similarly the internal capsule will be divided into four quadrants and its temporal-spatial correlations will be followed longitudinally. DTI values will be derived from each one of these individual structures. A robust DTI analysis tool will be developed for automatic analysis. This tool will also help in the fusion of multi-modal MRI data for a robust segmentation of the subregions of CC and 1C. The DTI measures, after accounting for the age and gender dependence will be correlated with the clinical measures.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AccountingAffectAgeAtrophicBrainClinicalCorpus CallosumCorticospinal TractsDataDemyelinationsDependenceDepthDiffusionDiffusion Magnetic Resonance ImagingDiseaseDistalEconomic BurdenEquilibriumFailureFemaleFiberGenderGliosisHandednessHeterogeneityImageImmune System DiseasesIndividualInflammationInternal CapsuleLesionLiteratureMagnetic Resonance ImagingMapsMeasuresModalityMonitorMultiple SclerosisNeuraxisNeurologicNoisePathologicPathologyPathway interactionsPeripheralPlacementProcessPublishingPyramidal TractsResearch PersonnelSchemeScoreSignal TransductionSliceSocietiesSpecificityStructureSystemTechniquesThickTimeTissuesWallerian DegenerationWaterage groupbasebrain tissuecomputerized data processingdisabilityhuman subjectin vivointerestmalesexsocialtoolwhite matter
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
800771594
UEI
ZUFBNVZ587D4
Project Start Date
13-July-2006
Project End Date
31-May-2010
Budget Start Date
01-June-2007
Budget End Date
31-May-2008
Project Funding Information for 2007
Total Funding
$291,992
Direct Costs
$196,628
Indirect Costs
$95,364
Year
Funding IC
FY Total Cost by IC
2007
National Institute of Neurological Disorders and Stroke
$291,992
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01NS052505-02
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