Multi-voxel spectral editing at 3T
Multi-voxel spectral editing at 3T
批准号:
10316240
负责人:
PETER B BARKER
金额:
$41.26万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-04-15 至 2024-10-31
关键词:
Aminobutyric AcidsAspartateBrainBrain regionChemicalsClinicalCommunitiesConsumptionData AnalysesData CollectionData SetDetectionDiseaseGlutamatesGlutathioneGoalsHeadHumanImaging TechniquesIndividualLocationMagnetic Resonance SpectroscopyMapsMeasurementMeasuresMethodologyMethodsMorphologic artifactsMotionN-acetylaspartateNeurosciencesNoiseNon-Invasive DetectionPhysiologic pulseProcessQuality ControlReproducibilityScanningSchemeSignal TransductionSpatial DistributionSystemTechniquesTechnologyTimeVisualizationarmascorbatebase editingclinical applicationcomputerized data processingdata acquisitionexperimental studyimaging approachimprovedin vivomodel developmentneuroimagingprospectivereconstructionsoftware developmentspectroscopic imagingtool
中文摘要
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英文摘要
PROJECT SUMMARY
Edited magnetic resonance spectroscopy allows the non-invasive detection of low-concentration
metabolites within the brain, free from overlap from other, more abundant compounds. Until recently, spectral-
editing techniques have generally focused on measuring individual metabolites in one brain region at a time
(for instance, the well-known ‘MEGA-PRESS’ method). However, this is a time-consuming approach which
severely limits clinical applicability when multiple metabolites and/or brain regions are involved. The main goal
of this proposal is therefore to develop and establish the reproducibility edited experiments that can detect
multiple edited molecules in multiple brain regions, all within a single acquisition.
We will develop multi-voxel localization techniques to combine with our recently developed multi-metabolite
editing methods, including the Hadamard-encoded ‘HERMES’ approach as well as the new ‘HERCULES’
method which allows for up to 13 metabolites to be simultaneously determined. For applications that may
require a limited number of voxels to be acquired, we will developed multi-band excitation and parallel
acquisition ‘PRIAM’ methods in combination with HERMES and HERCULES. For applications that require
greater spatial coverage and/or the ability to map out the spatial distribution of metabolite levels, edited MR
spectroscopic imaging (MRSI) techniques will be developed for use in combination with HERMES and
HERCULES editing. Since edited-MRSI is very sensitive to head motion and other instabilities, acquisition and
processing methods will be implemented for robust, motion-insensitive edited-MRSI.
Rigor and reproducibility will be carefully assessed; newly developed methodologies will be validated by
comparison to conventional measurements in the same subjects. Expected improvements in temporal signal-
to-noise ratios and reproducibility will also be measured. The resulting data acquisition and analysis tools will
be made available for dissemination to the clinical neuroscience and neuroimaging communities.
期刊论文(0)
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会议论文
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依托单位:
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Proton MRSI of Human Breast Cancer at 3 and 7 Tesla
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依托单位:
Proton MRSI of Human Breast Cancer at 3 and 7 Tesla
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依托单位:
Proton MRSI of Human Breast Cancer at 3 and 7 Tesla
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财政年份:2006
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依托单位:
BRAIN CHEMISTRY BY MR SPECTROSCOPIC IMAGING
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依托单位:
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依托单位:
国内基金
海外基金
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依托单位: