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ABSTRACT: Objective
To evaluate progressive white matter (WM) degeneration in amyotrophic lateral sclerosis (ALS).Methods
Sixty-six patients with ALS and 43 healthy controls were enrolled in a prospective, longitudinal, multicenter study in the Canadian ALS Neuroimaging Consortium (CALSNIC). Participants underwent a harmonized neuroimaging protocol across 4 centers that included diffusion tensor imaging (DTI) for assessment of WM integrity. Three visits were accompanied by clinical assessments of disability (ALS Functional Rating Scale-Revised [ALSFRS-R]) and upper motor neuron (UMN) function. Voxel-wise whole-brain and quantitative tract-wise DTI assessments were done at baseline and longitudinally. Correction for site variance incorporated data from healthy controls and from health
SUBMITTER: Kalra S
PROVIDER: S-EPMC7668555 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature