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Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
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Corticoefferent pathways in pure lower motor neuron disease: a diffusion tensor imaging study.
Angela Rosenbohm1, Hans-Peter Müller1, Annemarie Hübers1
1Department of Neurology, University of Ulm, Oberer Eselsberg 45, 89081, Ulm, Germany.
Journal of Neurology
|September 15, 2016
Summary
Diffusion tensor imaging reveals white matter alterations in lower motor neuron disease (LMND), particularly along the corticospinal tract. Fast-progressing LMND shows more significant changes, suggesting it may be a variant of amyotrophic lateral sclerosis (ALS).
Area of Science:
- Neuroimaging
- Neurology
- White Matter Diseases
Background:
- Diagnosing upper motor neuron (UMN) pathology in lower motor neuron disease (LMND) presents clinical challenges.
- Diffusion tensor imaging (DTI) offers in vivo insights into white matter integrity.
Purpose of the Study:
- To investigate white matter alterations in adult pure LMND using DTI.
- To compare fast and slow progressing LMND patients and explore tract-specific changes.
Main Methods:
- Whole-brain DTI and spatial statistics compared 37 LMND patients with 53 controls.
- Fractional anisotropy (FA) maps identified white matter structural differences.
- Fiber tracking analyzed tract-specific alterations based on ALS staging.
Main Results:
- LMND patients exhibited widespread FA reductions, predominantly in the corticospinal tract (CST).
- Fast progressing LMND showed greater CST involvement than slow progressors.
- Fast progressors also displayed alterations in ALS-related tracts beyond the CST.
Conclusions:
- Findings demonstrate corticoefferent fiber involvement in pure LMND, supporting its classification as a phenotypic variant of ALS.
- This suggests LMND patients should be managed similarly to ALS patients, including trial eligibility.
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