{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/45396"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/45396","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Imaging the local mechanical properties of the brain with high-resolution magnetic resonance elastography","abstract":"Mechanical properties of the human brain reflect the composition and organization of the complex tissue microstructure. Neurodegeneration involves alteration of this microstructure through a number of processes including neuronal cell death; glial matrix disruption and demyelination; and inflammatory cell infiltration. Assessment of neurological conditions requires imaging methods sensitive to microstructure and specific to neurodegenerative process. The noninvasive measurement of mechanical properties may provide this microstructural sensitivity necessary to improve early detection, differential diagnosis, and monitoring of disease progression. Magnetic resonance elastography (MRE) is a shear wave imaging technique that provides reliable, noninvasive estimates of tissue stiffness. MRE has been developed for many applications, and clinical practice has adopted MRE for the detection and staging of liver fibrosis. While the application of MRE to study the human brain in vivo has produced promising results, studies have been limited to reporting only global mechanical properties because of poor imaging spatial resolution and the complexity of the inverse problem associated with biomechanical property estimation. Increasing the clinical utility of MRE for assessing neurological disorders requires methodologies to obtain local estimates of brain tissue mechanical properties. The research presented in this dissertation focuses on the development of imaging strategies for MRE to enable the reliable estimation of local mechanical properties of the brain in vivo. Specifically, I present acquisition schemes for capturing shear displacement data at high-resolution. The use of these acquisitions on healthy human volunteers revealed neuroanatomical information previously unavailable from global MRE. Quantification of the local mechanical properties of the corpus callosum and corona radiata, two clinically relevant structures in the brain white matter, demonstrated that the measures agree with expected mechanical behavior based on underlying tissue microstructure. From these findings I conclude that high-resolution acquisitions provide reliable local property measures that may improve MRE studies of neurodegeneration and increase the utility of MRE as a clinical tool and quantitative microstructural imaging technique.","abstract_html":"Mechanical properties of the human brain reflect the composition and organization of the complex tissue microstructure. Neurodegeneration involves alteration of this microstructure through a number of processes including neuronal cell death; glial matrix disruption and demyelination; and inflammatory cell infiltration. Assessment of neurological conditions requires imaging methods sensitive to microstructure and specific to neurodegenerative process. The noninvasive measurement of mechanical properties may provide this microstructural sensitivity necessary to improve early detection, differential diagnosis, and monitoring of disease progression. Magnetic resonance elastography (MRE) is a shear wave imaging technique that provides reliable, noninvasive estimates of tissue stiffness. MRE has been developed for many applications, and clinical practice has adopted MRE for the detection and staging of liver fibrosis. While the application of MRE to study the human brain in vivo has produced promising results, studies have been limited to reporting only global mechanical properties because of poor imaging spatial resolution and the complexity of the inverse problem associated with biomechanical property estimation. Increasing the clinical utility of MRE for assessing neurological disorders requires methodologies to obtain local estimates of brain tissue mechanical properties. The research presented in this dissertation focuses on the development of imaging strategies for MRE to enable the reliable estimation of local mechanical properties of the brain in vivo. Specifically, I present acquisition schemes for capturing shear displacement data at high-resolution. The use of these acquisitions on healthy human volunteers revealed neuroanatomical information previously unavailable from global MRE. Quantification of the local mechanical properties of the corpus callosum and corona radiata, two clinically relevant structures in the brain white matter, demonstrated that the measures agree with expected mechanical behavior based on underlying tissue microstructure. From these findings I conclude that high-resolution acquisitions provide reliable local property measures that may improve MRE studies of neurodegeneration and increase the utility of MRE as a clinical tool and quantitative microstructural imaging technique.","abstract_has_math":false,"creators":["Johnson, Curtis L."],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Mechanical Engineering","degree_department":null,"school":null,"contributors":["Georgiadis, John G.","Sutton, Bradley P.","Liang, Zhi-Pei","Saif, M. Taher A.","Olivero, William C.","Wang, Huan"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2013,"date_issued":"2013-08-22T16:38:58Z","date_published":"2013-08-22T16:38:58Z","updated_at":"2026-07-22T22:25:34Z","subjects":["Magnetic resonance elastography","Brain","Stiffness","High-resolution","White matter","Corpus callosum"],"languages":["en"],"rights":["Copyright 2013 by Curtis Laurence Johnson"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/45396","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Georgiadis, John G.","Sutton, Bradley P.","Liang, Zhi-Pei","Saif, M. 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Neurodegeneration involves alteration of this microstructure through a number of processes including neuronal cell death; glial matrix disruption and demyelination; and inflammatory cell infiltration. Assessment of neurological conditions requires imaging methods sensitive to microstructure and specific to neurodegenerative process. The noninvasive measurement of mechanical properties may provide this microstructural sensitivity necessary to improve early detection, differential diagnosis, and monitoring of disease progression. Magnetic resonance elastography (MRE) is a shear wave imaging technique that provides reliable, noninvasive estimates of tissue stiffness. MRE has been developed for many applications, and clinical practice has adopted MRE for the detection and staging of liver fibrosis. While the application of MRE to study the human brain in vivo has produced promising results, studies have been limited to reporting only global mechanical properties because of poor imaging spatial resolution and the complexity of the inverse problem associated with biomechanical property estimation. Increasing the clinical utility of MRE for assessing neurological disorders requires methodologies to obtain local estimates of brain tissue mechanical properties. The research presented in this dissertation focuses on the development of imaging strategies for MRE to enable the reliable estimation of local mechanical properties of the brain in vivo. Specifically, I present acquisition schemes for capturing shear displacement data at high-resolution. The use of these acquisitions on healthy human volunteers revealed neuroanatomical information previously unavailable from global MRE. Quantification of the local mechanical properties of the corpus callosum and corona radiata, two clinically relevant structures in the brain white matter, demonstrated that the measures agree with expected mechanical behavior based on underlying tissue microstructure. From these findings I conclude that high-resolution acquisitions provide reliable local property measures that may improve MRE studies of neurodegeneration and increase the utility of MRE as a clinical tool and quantitative microstructural imaging technique.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2013-07-08T14:23:59Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Johnson_Curtis.pdf: 18371553 bytes, checksum: 04c399b74fb063e02226b13cfabf8d86 (MD5) Johnson_Curtis.pdf: 18371552 bytes, checksum: ac2869af64e12adc0e713045d0390e52 (MD5)","Made available in DSpace on 2013-08-22T16:38:58Z (GMT). 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Assessment of neurological conditions requires imaging methods sensitive to microstructure and specific to neurodegenerative process. The noninvasive measurement of mechanical properties may provide this microstructural sensitivity necessary to improve early detection, differential diagnosis, and monitoring of disease progression. Magnetic resonance elastography (MRE) is a shear wave imaging technique that provides reliable, noninvasive estimates of tissue stiffness. MRE has been developed for many applications, and clinical practice has adopted MRE for the detection and staging of liver fibrosis. While the application of MRE to study the human brain in vivo has produced promising results, studies have been limited to reporting only global mechanical properties because of poor imaging spatial resolution and the complexity of the inverse problem associated with biomechanical property estimation. Increasing the clinical utility of MRE for assessing neurological disorders requires methodologies to obtain local estimates of brain tissue mechanical properties. The research presented in this dissertation focuses on the development of imaging strategies for MRE to enable the reliable estimation of local mechanical properties of the brain in vivo. Specifically, I present acquisition schemes for capturing shear displacement data at high-resolution. The use of these acquisitions on healthy human volunteers revealed neuroanatomical information previously unavailable from global MRE. Quantification of the local mechanical properties of the corpus callosum and corona radiata, two clinically relevant structures in the brain white matter, demonstrated that the measures agree with expected mechanical behavior based on underlying tissue microstructure. From these findings I conclude that high-resolution acquisitions provide reliable local property measures that may improve MRE studies of neurodegeneration and increase the utility of MRE as a clinical tool and quantitative microstructural imaging technique.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2013-07-08T14:23:59Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Johnson_Curtis.pdf: 18371553 bytes, checksum: 04c399b74fb063e02226b13cfabf8d86 (MD5) Johnson_Curtis.pdf: 18371552 bytes, checksum: ac2869af64e12adc0e713045d0390e52 (MD5)","Made available in DSpace on 2013-08-22T16:38:58Z (GMT). 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