Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

The Topography of Brain Microstructural Damage in Amyotrophic Lateral Sclerosis Assessed Using Diffusion Tensor MR Imaging

The Topography of Brain Microstructural Damage in Amyotrophic Lateral Sclerosis Assessed Using... BACKGROUND AND PURPOSE: ALS leads to macrostructural (ie, cortical atrophy and hyperintensities along the corticospinal tract) and microstructural (ie, gray matter intrinsic damage) central nervous system abnormalities. We used a multimodal voxelwise imaging approach to assess microstructural changes independent of macrostructural volume loss in patients with ALS compared with HCs. MATERIALS AND METHODS: Twenty-three patients with ALS and 14 HCs were studied. Conventional imaging and DTI were performed. Images were processed by using SPM5 to assess measures of gray and white matter atrophy as well as microstructural damage (ie, MD and FA). DTI alterations independent of volume loss were investigated. RESULTS: When we accounted for both gray and white matter atrophy, patients with ALS showed increased MD values in several gray and white matter areas mainly located in the orbitofrontal and frontotemporal regions bilaterally, in the right genu of the corpus callosum, and in the right posterior limb of the internal capsule. When we accounted for white matter volume loss, patients with ALS showed decreased FA along the corticospinal tract bilaterally and in the left inferior frontal lobe relative to HCs. The MD of the orbitofrontal regions bilaterally was associated significantly with disease duration. CONCLUSIONS: In patients with ALS, DTI detects microstructural changes independent of brain tissue loss. The affected regions included both motor and extramotor areas. The extent of ALS-related DTI abnormalities was greater than that disclosed by the volumetric analysis. Abbreviations ALS amyotrophic lateral sclerosis ANCOVA analysis of covariance B0 DTI with no diffusion weighting BA Brodmann area BPM biological parametric mapping DARTEL Diffeomorphic Anatomical Registration using Exponentiated Lie algebra registration method DTI diffusion tensor imaging FA fractional anisotropy FLAIR fluid-attenuated inversion recovery FWHM full width at half maximum GM gray matter HC healthy control LL- and UL-MRC lower limb- and upper limb-Medical Research Council MD mean diffusivity MNI Montreal Neurological Institute MRC Medical Research Council scale r-ALSFRS ALS Functional Rating Scale-Revised SOD1 superoxide dismutase SPM statistical parametric mapping T1w T1-weighted T2w T2-weighted UMN upper motor neurons VBM voxel-based morphometry WM white matter http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png American Journal of Neuroradiology American Journal of Neuroradiology

The Topography of Brain Microstructural Damage in Amyotrophic Lateral Sclerosis Assessed Using Diffusion Tensor MR Imaging

Loading next page...
 
/lp/american-journal-of-neuroradiology/the-topography-of-brain-microstructural-damage-in-amyotrophic-lateral-cR590DyjIc

References

References for this paper are not available at this time. We will be adding them shortly, thank you for your patience.

Publisher
American Journal of Neuroradiology
Copyright
Copyright © 2011 by the American Society of Neuroradiology.
ISSN
0195-6108
eISSN
1936-959X
DOI
10.3174/ajnr.A2469
pmid
21680655
Publisher site
See Article on Publisher Site

Abstract

BACKGROUND AND PURPOSE: ALS leads to macrostructural (ie, cortical atrophy and hyperintensities along the corticospinal tract) and microstructural (ie, gray matter intrinsic damage) central nervous system abnormalities. We used a multimodal voxelwise imaging approach to assess microstructural changes independent of macrostructural volume loss in patients with ALS compared with HCs. MATERIALS AND METHODS: Twenty-three patients with ALS and 14 HCs were studied. Conventional imaging and DTI were performed. Images were processed by using SPM5 to assess measures of gray and white matter atrophy as well as microstructural damage (ie, MD and FA). DTI alterations independent of volume loss were investigated. RESULTS: When we accounted for both gray and white matter atrophy, patients with ALS showed increased MD values in several gray and white matter areas mainly located in the orbitofrontal and frontotemporal regions bilaterally, in the right genu of the corpus callosum, and in the right posterior limb of the internal capsule. When we accounted for white matter volume loss, patients with ALS showed decreased FA along the corticospinal tract bilaterally and in the left inferior frontal lobe relative to HCs. The MD of the orbitofrontal regions bilaterally was associated significantly with disease duration. CONCLUSIONS: In patients with ALS, DTI detects microstructural changes independent of brain tissue loss. The affected regions included both motor and extramotor areas. The extent of ALS-related DTI abnormalities was greater than that disclosed by the volumetric analysis. Abbreviations ALS amyotrophic lateral sclerosis ANCOVA analysis of covariance B0 DTI with no diffusion weighting BA Brodmann area BPM biological parametric mapping DARTEL Diffeomorphic Anatomical Registration using Exponentiated Lie algebra registration method DTI diffusion tensor imaging FA fractional anisotropy FLAIR fluid-attenuated inversion recovery FWHM full width at half maximum GM gray matter HC healthy control LL- and UL-MRC lower limb- and upper limb-Medical Research Council MD mean diffusivity MNI Montreal Neurological Institute MRC Medical Research Council scale r-ALSFRS ALS Functional Rating Scale-Revised SOD1 superoxide dismutase SPM statistical parametric mapping T1w T1-weighted T2w T2-weighted UMN upper motor neurons VBM voxel-based morphometry WM white matter

Journal

American Journal of NeuroradiologyAmerican Journal of Neuroradiology

Published: Aug 1, 2011

References