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DETECTING CEREBRAL DEGENERATION IN ALS USING A MULTICENTRE APPLICATION OF 3D TEXTURE ANALYSIS

  • Author / Creator
    Chunn, Michael
  • Amyotrophic lateral sclerosis (ALS) is a highly heterogeneous disease in terms of its clinical presentation, progression, and detected pathology in the body. It is a multi-system degenerative disorder, though a diagnosis is made based on the presence of both upper motor neuron (UMN) and lower motor neuron (LMN) degeneration. However, the disease rests on a spectrum of both motor and cognitive systems degeneration. ALS is fatal with a typical course of 2-5 years. The diagnostic process is long and complicated, often taking about one year from symptom onset. For these reasons, ALS needs a biomarker – an objective measure of disease presence and progression. This would simplify diagnosis and allow treatment and drug trials to be implemented earlier in the disease process. Studies have explored neuroimaging as a source of potential biomarkers. Techniques such as voxel-based morphometry (VBM) and diffusion tensor imaging (DTI) have been previously used to study cerebral degeneration but have yet to be refined as highly sensitive and specific diagnostic tools. A more novel tool called texture analysis (TA) has recently been applied to various diseases as a means to examine pathology in vivo. Furthermore, TA has been applied in two previous studies of ALS, finding high sensitivity and specificity in differentiating patients from controls. TA examines both grey matter and white matter in the brain simultaneously by quantifying the relationships between grey level intensities in neighbouring voxels of a 3D magnetic resonance image. It does so using T1-weighted images – often acquired as part of the diagnostic process. The present study aims to examine cerebral degeneration in ALS patients as detected by TA in a multicentre dataset, and how degeneration correlates with clinical signs of UMN degeneration. Furthermore, this study aims to test the reliability of TA both within and between sites of acquisition to further support the future implementation of TA as a clinical biomarker.

  • Subjects / Keywords
  • Graduation date
    Fall 2018
  • Type of Item
    Thesis
  • Degree
    Master of Science
  • DOI
    https://doi.org/10.7939/R3C24R40C
  • License
    Permission is hereby granted to the University of Alberta Libraries to reproduce single copies of this thesis and to lend or sell such copies for private, scholarly or scientific research purposes only. Where the thesis is converted to, or otherwise made available in digital form, the University of Alberta will advise potential users of the thesis of these terms. The author reserves all other publication and other rights in association with the copyright in the thesis and, except as herein before provided, neither the thesis nor any substantial portion thereof may be printed or otherwise reproduced in any material form whatsoever without the author's prior written permission.