Advanced MRI methods for probing disease severity and functional decline in multiple sclerosis
dc.contributor.advisor | Zhang, Yunyan | |
dc.contributor.author | Oladosu, Olayinka Adeoluwa | |
dc.contributor.committeemember | Joshi, Manish | |
dc.contributor.committeemember | Dunn, Jeffrey Frank | |
dc.contributor.committeemember | Frayne, Richard | |
dc.contributor.committeemember | Le, Lawrence Trong-Huan | |
dc.date.accessioned | 2023-12-14T22:03:35Z | |
dc.date.available | 2023-12-14T22:03:35Z | |
dc.date.issued | 2023-12-14 | |
dc.description.abstract | Multiple sclerosis (MS) is a chronic and severe disease of the central nervous system characterized by complex pathology including inflammatory demyelination and neurodegeneration. MS impacts >2.8 million people worldwide, with most starting with a relapsing-remitting form (RRMS) in young adulthood, and many of them worsening to a secondary-progressive course (SPMS) despite treatment. So, there is a clear need for improved disease characterization. MRI is an ideal tool for non-invasive assessment of MS pathology, but there is still no established measure of disease activity and functional consequences. This project aims to overcome the challenge by developing novel imaging measures based on brain diffusion MRI and phase congruency texture analysis of conventional MRI. Through advanced modeling and analysis of clinically feasible brain MRI, this thesis investigates whether and how the derived measures differentiate MS pathology types and disease severity and predict functional outcomes in MS. The overall process has led to important technical innovations in several aspects. These include: innovative modeling of simple diffusion acquisitions to generate high angular resolution diffusion imaging (HARDI) measures; new optimization and harmonization techniques for diffusion MRI; innovative neural network models to create new diffusion data for comprehensive HARDI modeling; and novel methods and a graphic user interface for optimizing phase congruency analyses. Assisted by different machine learning methods, collective findings show that advanced measures from both diffusion MRI and phase congruency are highly sensitive to subtle differences in MS pathology, which differentiate disease severity between RRMS and SPMS through multi-dimensional analyses including chronic active lesions, and predict functional outcomes especially in physical and neurocognitive domains. These results are clinically translational and the new measures and techniques can help improve the evaluation and management of both MS and similar diseases. | |
dc.identifier.citation | Oladosu, O. A. (2023). Advanced MRI methods for probing disease severity and functional decline in multiple sclerosis (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. | |
dc.identifier.uri | https://hdl.handle.net/1880/117738 | |
dc.identifier.uri | https://doi.org/10.11575/PRISM/42581 | |
dc.language.iso | en | |
dc.publisher.faculty | Graduate Studies | |
dc.publisher.institution | University of Calgary | |
dc.rights | University of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission. | |
dc.subject | Multiple Sclerosis | |
dc.subject | Diffusion MRI | |
dc.subject | Texture Analysis | |
dc.subject.classification | Neuroscience | |
dc.subject.classification | Radiology | |
dc.title | Advanced MRI methods for probing disease severity and functional decline in multiple sclerosis | |
dc.type | doctoral thesis | |
thesis.degree.discipline | Medicine – Neuroscience | |
thesis.degree.grantor | University of Calgary | |
thesis.degree.name | Doctor of Philosophy (PhD) | |
ucalgary.thesis.accesssetbystudent | I do not require a thesis withhold – my thesis will have open access and can be viewed and downloaded publicly as soon as possible. |