Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging

T2 relaxation imaging can be used to measure signal from water trapped between myelin bilayers; the ratio of myelin water signal to total water is termed the myelin water fraction (MWF). First, results from multi-component T2 relaxation and diffusion tensor imaging (DTI) were compared for 19 mult...

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Main Author: Kolind, Shannon Heather
Format: Others
Language:English
Published: University of British Columbia 2008
Subjects:
T2
Online Access:http://hdl.handle.net/2429/2922
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-BVAU.-29222013-06-05T04:17:18ZMyelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imagingKolind, Shannon HeatherMagnetic resonance imagingMyelinMultiple sclerosisT2T2 relaxation imaging can be used to measure signal from water trapped between myelin bilayers; the ratio of myelin water signal to total water is termed the myelin water fraction (MWF). First, results from multi-component T2 relaxation and diffusion tensor imaging (DTI) were compared for 19 multiple sclerosis (MS) subjects at 1.5 T to better understand how each measure is affected by pathology. In particular, it was determined that the detection of a long-T2 signal within an MS lesion may be indicative of a different underlying pathology than is present in lesions without long-T2 signal. Next, the single-slice T2 relaxation measurement was implemented, refined, and validated at 3.0 T. Scan parameters were varied for phantoms and in-vivo brain, and changes in multi-exponential fit residuals and T2 distribution-derived parameters such as MWF were monitored to determine which scan parameters minimized artifacts. Measurements were compared between 1.5 T and 3.0 T for 10 healthy volunteers. MWF maps were qualitatively similar between field strengths. MWFs were significantly higher at 3.0 T than at 1.5 T, but with a strong correlation between measurements at the different field strengths. Due to long acquisition times, multi-component T2 relaxation has thus far been clinically infeasible. The next study aimed to validate a new 3D multi-component T2 relaxation imaging technique against the 2D single-slice technique most commonly used. Ten healthy volunteers were scanned with both the 2D single-slice and 3D techniques. MWF maps were qualitatively similar between scans. MWF values were highly correlated between the acquisition methods. Although MWF values were generally lower using the 3D technique, they were only significantly so for peripheral brain structures, likely due to increased sensitivity of slab-selective refocusing pulses used for the 3D approach. The 3D T2 relaxation sequence was then applied to the study of MS to take advantage of the increased brain coverage. Thirteen MS subjects and 11 controls underwent T2 relaxation and DTI examinations to produce histograms of MWF and several DTI-derived metrics. MS MWF histograms differed considerably from those of controls, and differences in MS MWF histograms did not mirror differences in DTI histograms relative to matched controls.University of British Columbia2008-12-16T18:48:49Z2008-12-16T18:48:49Z20082008-12-16T18:48:49Z2009-05Electronic Thesis or Dissertation3580011 bytesapplication/pdfhttp://hdl.handle.net/2429/2922eng
collection NDLTD
language English
format Others
sources NDLTD
topic Magnetic resonance imaging
Myelin
Multiple sclerosis
T2
spellingShingle Magnetic resonance imaging
Myelin
Multiple sclerosis
T2
Kolind, Shannon Heather
Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
description T2 relaxation imaging can be used to measure signal from water trapped between myelin bilayers; the ratio of myelin water signal to total water is termed the myelin water fraction (MWF). First, results from multi-component T2 relaxation and diffusion tensor imaging (DTI) were compared for 19 multiple sclerosis (MS) subjects at 1.5 T to better understand how each measure is affected by pathology. In particular, it was determined that the detection of a long-T2 signal within an MS lesion may be indicative of a different underlying pathology than is present in lesions without long-T2 signal. Next, the single-slice T2 relaxation measurement was implemented, refined, and validated at 3.0 T. Scan parameters were varied for phantoms and in-vivo brain, and changes in multi-exponential fit residuals and T2 distribution-derived parameters such as MWF were monitored to determine which scan parameters minimized artifacts. Measurements were compared between 1.5 T and 3.0 T for 10 healthy volunteers. MWF maps were qualitatively similar between field strengths. MWFs were significantly higher at 3.0 T than at 1.5 T, but with a strong correlation between measurements at the different field strengths. Due to long acquisition times, multi-component T2 relaxation has thus far been clinically infeasible. The next study aimed to validate a new 3D multi-component T2 relaxation imaging technique against the 2D single-slice technique most commonly used. Ten healthy volunteers were scanned with both the 2D single-slice and 3D techniques. MWF maps were qualitatively similar between scans. MWF values were highly correlated between the acquisition methods. Although MWF values were generally lower using the 3D technique, they were only significantly so for peripheral brain structures, likely due to increased sensitivity of slab-selective refocusing pulses used for the 3D approach. The 3D T2 relaxation sequence was then applied to the study of MS to take advantage of the increased brain coverage. Thirteen MS subjects and 11 controls underwent T2 relaxation and DTI examinations to produce histograms of MWF and several DTI-derived metrics. MS MWF histograms differed considerably from those of controls, and differences in MS MWF histograms did not mirror differences in DTI histograms relative to matched controls.
author Kolind, Shannon Heather
author_facet Kolind, Shannon Heather
author_sort Kolind, Shannon Heather
title Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
title_short Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
title_full Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
title_fullStr Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
title_full_unstemmed Myelin water imaging : development at 3.0T, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
title_sort myelin water imaging : development at 3.0t, application to the study of multiple sclerosis, and comparison to diffusion tensor imaging
publisher University of British Columbia
publishDate 2008
url http://hdl.handle.net/2429/2922
work_keys_str_mv AT kolindshannonheather myelinwaterimagingdevelopmentat30tapplicationtothestudyofmultiplesclerosisandcomparisontodiffusiontensorimaging
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