2026-09-19T12:18:27Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/1284112021-07-05T14:03:20Zcom_1721.1_7582com_1721.1_7581col_1721.1_131023
Jacob White.
Arango, Nicolas(Nicolas S.)
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science.
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
2020-11-06T21:08:36Z
2020-11-06T21:08:36Z
2020
2020
https://hdl.handle.net/1721.1/128411
1203061574
Thesis: S.M., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, February, 2020
Cataloged from PDF version of thesis. [d̳e̳l̳t̳a̳] in title on title page appears as upper case Greek letter.
Includes bibliographical references (pages 33-35).
This work develops sequence-phase optimal (SPO) [delta]B₀ shimming methods to reduce lipid contamination and improve brain metabolite spectra in proton spectroscopic imaging. A rapidly reconfigurable 32-channel, local-multi-coil-shim-array is used to enhance lipid suppression and narrow metabolite linewidth in magnetic resonance spectroscopic imaging (MRSI) of the brain. The array is optimally reconfigured dynamically during each MRSI repetition period, first during the lipid-suppression phase, by widening the spectral gap between spatially separate lipid and metabolite regions, and then to narrow metabolite linewidth during readout, by brain-only [delta]B₀ homogenization. This sequence-phase-optimal (SPO) shimming approach is demonstrated on four volunteer subjects using a commercial 3T MRI outfitted with a 32-channel integrated RF receive and local multi-coil shim array. This proposed sequence-phase-optimal shimming significantly improves brain-metabolite MRSI in vivo, as measured by lipid suppression, brain metabolite chemical shift, and line widths. The time required to compute patient specific SPO shims negligibly impacted scan time. Sequence-phase-optimal shimming reduced lipid energy in the brain volume across four subjects by 88%, improved NAA FWHM by 23%, and dramatically reduced lipid ringing artifacts in quantified NAA and Glutamate metabolites, without increasing scan time or SAR.
by Nicolas Arango.
S.M.
S.M. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
35 pages
eng
Massachusetts Institute of Technology
MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.
http://dspace.mit.edu/handle/1721.1/7582
Electrical Engineering and Computer Science.
Sequence-phase optimal (SPO) [d̳e̳l̳t̳a̳]B₀ field control for lipid suppression and homogeneity for brain magnetic resonance spectroscopic imaging
Thesis
application/pdf
2020-11-06T21:08:34Z
Publication
Master
EECS
unknown
unknown
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<Abstract>This work develops sequence-phase optimal (SPO) [delta]B₀ shimming methods to reduce lipid contamination and improve brain metabolite spectra in proton spectroscopic imaging. A rapidly reconfigurable 32-channel, local-multi-coil-shim-array is used to enhance lipid suppression and narrow metabolite linewidth in magnetic resonance spectroscopic imaging (MRSI) of the brain. The array is optimally reconfigured dynamically during each MRSI repetition period, first during the lipid-suppression phase, by widening the spectral gap between spatially separate lipid and metabolite regions, and then to narrow metabolite linewidth during readout, by brain-only [delta]B₀ homogenization. This sequence-phase-optimal (SPO) shimming approach is demonstrated on four volunteer subjects using a commercial 3T MRI outfitted with a 32-channel integrated RF receive and local multi-coil shim array. This proposed sequence-phase-optimal shimming significantly improves brain-metabolite MRSI in vivo, as measured by lipid suppression, brain metabolite chemical shift, and line widths. The time required to compute patient specific SPO shims negligibly impacted scan time. Sequence-phase-optimal shimming reduced lipid energy in the brain volume across four subjects by 88%, improved NAA FWHM by 23%, and dramatically reduced lipid ringing artifacts in quantified NAA and Glutamate metabolites, without increasing scan time or SAR.</Abstract>
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