qBead Assessment of miRNA in Alzheimer's Disease
qBead Assessment of miRNA in Alzheimer's Disease
批准号:
8319370
负责人:
BRUCE E. SELIGMANN
金额:
$10.92万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-08-15 至 2013-07-31
关键词:
Alzheimer&aposs DiseaseArchivesAreaAutopsyBiological AssayBiological MarkersBiopsyBlood VesselsBrainBrain PathologyBrain regionCellsCerebrovascular DisordersCytolysisDementiaDiagnosisDiagnosticDiseaseDisease ProgressionFormalinFreezingGene ExpressionGene Expression ProfileHealthLifeLiteratureMeasurementMeasuresMessenger RNAMethodsMicroRNAsNuclease Protection AssaysParaffin EmbeddingParietal LobeParkinson DiseaseParkinson&aposs DementiaPatientsPeripheral Blood Mononuclear CellPhasePlasmaPractice GuidelinesPublicationsReagentReportingResearch InstituteResourcesSamplingSerumSliceSlideSmall Business Innovation Research GrantTarget PopulationsTemporal LobeTestingThe SunThickTissue BankingTissue BanksTissue SampleTissuesTrainingVascular Dementiabasebrain tissuedisorder controldrug discoveryfrontal lobemind controlnovelnovel therapeuticspatient populationpreventproduct developmentprogramssuccesstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): miRNA biomarkers related to Alzheimer's disease (AD) that may be useful as a diagnostic tool or in elucidating the mechanisms of disease and discovery of novel therapeutics will be identified using a novel whole transcriptome qBead" X-MAP-based assay (not yet launched commercially). Biomarkers will be identified from brain formalin fixed (FFPE) tissue and matched serum samples of AD patients, patients diagnosed Parkinson's disease and dementia (PD), patients with cerebrovascular disease neuropathologically diagnosed as vascular dementia (VaD), and normal controls (NC). The results will be validated using matched frozen tissue and both the qBead assay and PCR. The qBead X-MAP assay utilizes the quantitative Nuclease Protection Assay (qNPA") and measures both miRNA and mRNA. It is very precise and sensitive. This program will exploit the qBead assay to validate the utility of FFPE and serum for identification of AD biomarkers, to confirm recent reports of altered miRNA levels in frozen brain of AD patients, and to provide an early example of an application of the qBead whole transcriptome miRNA assay. In Phase II mRNA biomarkers will be included and the studies expanded to a larger training set of AD, PD, VaD and NC FFPE, serum, buffy coat, and plasma samples to expand the biomarker set and then test an independent set of samples to confirm/validate the biomarkers.
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