Simultaneous multi-slice GABA-edited MRSI in the developing brain
Simultaneous multi-slice GABA-edited MRSI in the developing brain
批准号:
9372604
负责人:
Yan Li
金额:
$23.78万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-07-15 至 2019-06-30
关键词:
37 weeks gestationAdultAffectAgeAminobutyric AcidsAnatomyAreaBiochemicalBirth traumaBrainBrain DiseasesBrain InjuriesBrain regionBreathingCenters for Disease Control and Prevention (U.S.)Cerebral PalsyChildClinicalClinical assessmentsCognitionCommunitiesCongenital AbnormalityDataDetectionDevelopmentDiagnosisDiffusionDiseaseEnvironmentEvaluationFaceFamilyFunctional ImagingGlutamatesGlutamineGoalsHealthHealthcareImageInborn Errors of MetabolismInfantLearningLifeLocationMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMediator of activation proteinMetabolicMethodologyMethodsNeurologicNeurotransmittersNewborn InfantOutcomeOutcome MeasurePatientsPhasePhysiologic pulsePopulationPregnancyPremature InfantPropertyRecruitment ActivityReproducibilityResearchResolutionRestRiskRoleScanningShapesSignal TransductionSliceSpectrum AnalysisTechniquesTechnologyTestingTherapeutic InterventionTimeTreatment EfficacyVisitanatomic imagingbasebrain metabolismclinically relevantcognitive developmentdata acquisitiondesigndisabilityeconomic costemotional distressfeedingfollow-upgamma-Aminobutyric Acidhealthy volunteerhigh riskimprovedimproved outcomein vivointerestmetabolic imagingmetabolic profilenervous system disorderneurodevelopmentnovelpatient populationprematurereceptorreconstructionspectroscopic imagingsymposiumtreatment strategyvolunteer
中文摘要
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英文摘要
Project Summary
Metabolic imaging in newborns has proven useful for clinical assessment of children with brain injuries,
extrinsic and inborn errors of metabolism, and disorders of brain maturation. As the brain matures, the
metabolic profiles also change. Υ-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in
the mature brain, is an excitatory mediator during early brain development, and showed difference between
preterm and term infants. Single voxel spectroscopic (SVS) acquisition is the most commonly available
methodology for non-invasively investigating brain metabolism but covering multiple anatomical regions is
challenging because each of the acquisitions takes approximately 5 minutes. In this proposed project, we will
leverage the most recent advances in multi-channel phased arrays with RF technology to develop multi-slice
GABA-edited 2D MR spectroscopy imaging (MRSI) with high spatial resolution that is acquired simultaneously
at multiple locations in under 5 minutes of scan time. Metabolite accuracy compared to standard SVS and test-
retest reliability will be conducted on scans from 10 healthy adult volunteers with one week apart. We will
recruit 30 preterm patients. They will undergo their imaging exams when they are clinically stable and before
discharge, and will return for follow-up visits at the 6-month corrected age. Metabolic profiles, along with the
convention and advanced MR imaging parameters, will be correlated to the clinical outcome measures. The
fast MRSI data acquisition being developed will provide capabilities for evaluating preterm infants and will also
be important for diagnosis and assessment of a much broader range of neurological diseases.
According to CDC, there are more than 500,000 babies in the US each year that are born prematurely (less
than 37 weeks gestation). Babies born between 24 and 31 weeks gestation are five times as likely as full-term
infants to have a birth defect, and infants born even a few weeks early are three times higher. Those who
survive face the risk of life long health consequences, including difficulties in breathing and feeding, cerebral
palsy, and problems in learning. Developing criteria of evaluating and identifying temporal and spatial changes
in metabolites are critical for evaluating brain development in preterm infants. The proposed simultaneous
multi-slice MRSI acquisition will enable assessment of a wider area of the brain within a clinical feasible time,
allow longitudinal detection of the metabolic profiles in the same locations after voxel shift, and provide
averaged spectra in irregular shapes, which will improve patient evaluation. The targeted patient population of
newborns would benefit immediately from the increased mapping of metabolic information, while maintaining
scan time, minimizing the time spent outside of NICU and reducing potential risk.
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