Difference between revisions of "2014 Project Week:TBIdemyelination"
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==Key Investigators== | ==Key Investigators== | ||
| − | + | Andrei Irimia, PhD (Institute for Neuroimaging and Informatics, University of Southern California) | |
| + | |||
| + | SY Matthew Goh, BS (Institute for Neuroimaging and Informatics, University of Southern California) | ||
| + | |||
| + | Carinna M. Torgerson, BS (Institute for Neuroimaging and Informatics, University of Southern California) | ||
| + | |||
| + | John D. Van Horn, PhD (Institute for Neuroimaging and Informatics, University of Southern California) | ||
==Project Description== | ==Project Description== | ||
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<div style="width: 27%; float: left; padding-right: 3%;"> | <div style="width: 27%; float: left; padding-right: 3%;"> | ||
<h3>Objective</h3> | <h3>Objective</h3> | ||
| − | * | + | * To determine the extent and location of axonal demyelination in the gray matter and white matter of the brain for a group of TBI patients |
| + | * We seek to understand how mapping demyelination in TBI may help to elucidate the relationship between neuropsychological deficits and structural brain changes due to this condition, with potential relevance to personalized treatment and rehabilitation. | ||
</div> | </div> | ||
<div style="width: 27%; float: left; padding-right: 3%;"> | <div style="width: 27%; float: left; padding-right: 3%;"> | ||
<h3>Approach, Plan</h3> | <h3>Approach, Plan</h3> | ||
| − | * | + | * the study will be implemented in accordance with the Declaration of Helsinki and with approval from the UCLA and USC Institutional Review Boards |
| + | * multimodal neuroimaging data acquired from patients admitted to the Neurointensive Care Unit of the UCLA Ronald Reagan Medical Center will be used | ||
| + | * a Siemens Magnetom Trio Tim scanner with a magnetic field strength of 3 T was used to acquire T1- and T2-weighted magnetic resonance imaging (MRI) volumes both acutely and chronically (at several days as well as ~6 months post-injury, respectively) | ||
| + | * affine co-registration of all acquired MRI volumes will be performed within each subject using 3D Slicer | ||
| + | * the extent of axonal demyelination will be estimated based on the ratio of voxel intensities between T1 and T2 volumes following the methodology of Glasser & Van Essen (Journal of Neuroscience, 2011, vol. 31, p. 11597). | ||
| + | * myelin content measurements will be discarded from the analysis for brain regions which exhibit pathology-related alterations in voxel intensity due to the presence of acute trauma, resulting in an analysis of healthy-appearing brain regions only. | ||
</div> | </div> | ||
<div style="width: 27%; float: left; padding-right: 3%;"> | <div style="width: 27%; float: left; padding-right: 3%;"> | ||
Revision as of 19:57, 10 December 2013
Home < 2014 Project Week:TBIdemyelination
Key Investigators
Andrei Irimia, PhD (Institute for Neuroimaging and Informatics, University of Southern California)
SY Matthew Goh, BS (Institute for Neuroimaging and Informatics, University of Southern California)
Carinna M. Torgerson, BS (Institute for Neuroimaging and Informatics, University of Southern California)
John D. Van Horn, PhD (Institute for Neuroimaging and Informatics, University of Southern California)
Project Description
Objective
- To determine the extent and location of axonal demyelination in the gray matter and white matter of the brain for a group of TBI patients
- We seek to understand how mapping demyelination in TBI may help to elucidate the relationship between neuropsychological deficits and structural brain changes due to this condition, with potential relevance to personalized treatment and rehabilitation.
Approach, Plan
- the study will be implemented in accordance with the Declaration of Helsinki and with approval from the UCLA and USC Institutional Review Boards
- multimodal neuroimaging data acquired from patients admitted to the Neurointensive Care Unit of the UCLA Ronald Reagan Medical Center will be used
- a Siemens Magnetom Trio Tim scanner with a magnetic field strength of 3 T was used to acquire T1- and T2-weighted magnetic resonance imaging (MRI) volumes both acutely and chronically (at several days as well as ~6 months post-injury, respectively)
- affine co-registration of all acquired MRI volumes will be performed within each subject using 3D Slicer
- the extent of axonal demyelination will be estimated based on the ratio of voxel intensities between T1 and T2 volumes following the methodology of Glasser & Van Essen (Journal of Neuroscience, 2011, vol. 31, p. 11597).
- myelin content measurements will be discarded from the analysis for brain regions which exhibit pathology-related alterations in voxel intensity due to the presence of acute trauma, resulting in an analysis of healthy-appearing brain regions only.
