MR Measured Oxygen Metabolic Index in Ischemic Stroke
MR Measured Oxygen Metabolic Index in Ischemic Stroke
批准号:
7869506
负责人:
Weili Lin
金额:
$22.46万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-08-07 至 2012-08-31
关键词:
AffectAlbuminsAnimalsBody TemperatureBrain regionCerebral IschemiaCerebrumClinicalCoupledCyclotronsErythrocytesEvolutionExhibitsFeverGeneticHematocrit procedureHousingHumanImageInfarctionInjection of therapeutic agentInjuryIschemiaIschemic StrokeKnowledgeLabelLeadLesionLifeLong-Evans RatsMagnetic Resonance ImagingMapsMeasuresMedical centerMetabolicMiddle Cerebral Artery OcclusionModelingOutcomeOxygenPatientsPhysiologicalPositron-Emission TomographyPredictive ValuePrincipal InvestigatorProtocols documentationRat StrainsRattusReperfusion TherapyReportingSerumSimulateStrokeSystemTechnetium 99mTechnetium Tc 99m Aggregated AlbuminTechnologyTestingTimeTissue ViabilityTissuesTracerWeightWistar Ratsacute strokebasebrain tissueclinically relevantimprovedin vivoindexinginjuredischemic lesionnatural hypothermiaprogramsresearch studyresponsesingle photon emission computed tomographysuccesstool
中文摘要
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英文摘要
Several lines of evidence derived from positron emission tomography (PET) studies suggest that
measures of cerebral metabolic rate of oxygen utilization (CMRO2) provide an indication of brain tissue
viability during cerebral ischemia. Although PET is a currently available technology to measure CMRO2, the
need for an onsite cyclotron has limited its availability to only a few medical centers. Therefore, alternative
approaches capable of providing similar physiological information as that of PET CMRO2 could have
profound clinical implications. Towards this end, we have recently developed an MR imaging approach
capable of measuring cerebral oxygen metabolic activity, which we have termed MR cerebral oxygen
metabolic index (MR_COMI). Although physically different from PET CMRO2, preliminary results based on
MR_COMI are encouraging, suggesting that this approach may indeed reveal similar physiological
information as that of PET CMRO2. However, in order to determine if MR_COMI can delineate tissue
viability during ischemia, a direct comparison between MR_COMI predicted tissue infarction and final tissue
outcome under experimental conditions that are highly clinically relevant is of paramount importance.
Therefore, the overall focus of this application is to first determine an MR_COMI threshold for irreversible
injury and subsequently use this MR_COMI threshold to assess dynamic temporal and spatial evolution of
MR_COMI defined lesions in response to cerebral ischemia (Aim 1) and second, empirically determine the
predictive value of MR_COMI threshold, exploiting experimental conditions known to alter infarct volume
(Aim 2). In addition, since this newly developed MR approach requires knowledge of regional cerebral
hematocrit (Hct) which may change during cerebral ischemia, a parallel aim is proposed (Aim 3) to
determine how cerebral ischemia induces alterations of cHct using small animal single photon emission
computed tomography (SAI SPECT). Specifically, serial injections of two tracers: Tc-99m labeled red blood
cells and Tc-99m labeled serum human albumin will be used to obtained SPECT images for the estimates
of cHct. The success of the proposed studies will demonstrate that the newly developed MR approach is
capable of delineate irreversibly injured from viable tissues under cerebral ischemia and may offer a tool for
individualized treatment of acute stroke patients.
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海外基金