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Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
Characteristics of abnormal diffusivity in normal-appearing white matter investigated with diffusion tensor MR
M I Makki1, D C Chugani, J Janisse
1Carman and Ann Adams Department of Pediatrics, Children's Hospital of Michigan, Detroit, MI 48201, USA. malek@pet.wayne.edu
AJNR. American Journal of Neuroradiology
|September 26, 2007
Summary
Diffusion tensor imaging (DTI) revealed microstructural white matter (WM) changes in children with tuberous sclerosis complex (TSC). These findings suggest myelin packing alterations and gliosis in normal-appearing WM, even outside visible lesions.
Area of Science:
- Neuroimaging
- White Matter Microstructure
- Diffusion Tensor Imaging
Background:
- Tuberous sclerosis complex (TSC) is associated with various structural abnormalities.
- White matter (WM) changes may exist in TSC even when appearing normal on conventional MRI.
Purpose of the Study:
- To investigate in vivo microstructural changes in normal-appearing white matter (NAWM) in children with TSC using diffusion tensor imaging (DTI).
- To determine if DTI abnormalities in NAWM of TSC patients differ across diffusion directions.
Main Methods:
- DTI was used to assess diffusivity and anisotropy in NAWM of 6 children with TSC and 12 controls.
- Specific WM regions analyzed included the internal capsule, external capsule, and corpus callosum.
- Analysis focused on major, middle, and minor eigenvalues to evaluate directional diffusion differences.
Main Results:
- NAWM in TSC patients showed significantly increased mean diffusivity and decreased anisotropy compared to controls.
- The increase in diffusivity was more pronounced in directions perpendicular to axons (minor and middle eigenvalues).
Conclusions:
- Microstructural changes, including decreased anisotropy and increased radial/longitudinal diffusivities, were found in NAWM of TSC patients.
- These axonal changes likely relate to myelin packing alterations, gliosis, and myelination defects characteristic of TSC.

