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Biomarkers Core (Core E)

Biomarkers Core (Core E)
生物标志物核心(核心 E)
批准号:
10541806
负责人:
STEVEN E ARNOLD
金额:
$15.01万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
未结题
起止时间:
2010-07-15 至 2025-12-31
关键词:
AgeAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease pathologyAlzheimer’s disease biomarkerAmyloidAmyloid beta-ProteinAutomobile DrivingBiologicalBiological AssayBiological MarkersBloodBlood BanksBlood VesselsCCL2 geneCCL4 geneCell LineCerebrospinal FluidClinicalCognitionCohort StudiesCollaborationsCollectionComplement 1qComplexDNADataDementiaDiagnosisEnzyme-Linked Immunosorbent AssayFunctional disorderGrantIL8 geneImmune responseImmunoassayImpaired cognitionIndividualInflammationInflammatoryInjuryInterferon Type IIInterleukin-1 betaInterleukin-2Interleukin-4Interleukin-6KDR geneLaboratoriesLightMatrix MetalloproteinasesMeasurementMeasuresMetabolicMethodsMicroRNAsMissionMolecularMonitorNerve DegenerationNeurologyNeurosciencesPGF geneParticipantPathologyPharmaceutical PreparationsPhysical activityPlasmaPositron-Emission TomographyPreventionPreventive treatmentProceduresProcessProgram Research Project GrantsPsychiatryRNARecording of previous eventsResearchResearch PersonnelRoboticsSamplingScientistSeasonsSerumSiteSpecificitySymptomsSynapsesTNF geneTechnologyTestingTimeVEGFC geneVascular Cell Adhesion Molecule-1Vascular Endothelial Growth Factor CVascular Endothelial Growth Factor DVascular Endothelial Growth FactorsWhole BloodWorkaging brainbiobankbiomarker panelblood-based biomarkerbrain healthcardiovascular risk factorcohortdesignexperiencefunctional declineinflammatory markerinterestneurofilamentneuroimagingneuron lossneuropathologynew technologynovel markerresponse to injurysingle moleculetau Proteinstreatment responsevascular injury

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中文摘要
翻译
摘要:核心e -生物标志物核心。生物标记核心支持哈佛老化大脑研究
英文摘要
SUMMARY: CORE E- BIOMARKER CORE. The Biomarker Core supports the Harvard Aging Brain Study (HABS) Program Project Grant (PPG) by processing and banking blood (plasma, serum, whole blood, buffy coat, RNA, miRNA, DNA and cell lines) and cerebrospinal fluid (CSF) samples (Aim 1) collected by the Clinical Core (Core B) from individuals (ages 50 to 94). Assays will be conducted on these biofluids to generate data on amyloid-b ("A"), tau ("T") and neurodegeneration ("N") (Aim 2) and data on vascular injury and immune response factors (Aim 3) for analysis by the Projects. The newly established Biomarker Core for HABS includes over 1300 biofluid samples (blood and CSF) from 373 participants in Grant Cycles 1 and 2, and will bank additional longitudinal samples over the next cycle. Bloods have been processed into plasma, serum, whole blood, buffy coat, RNA, miRNA, DNA and cell lines, and CSFs are collected, processed and stored according to best practices to minimize pre-analytical variability. ATN data has been generated using ultra- sensitive single molecule array (Simoa) technology with assays for Ab42, NT1 tau and neurofilament-light (NfL) in all samples to date as well as modifying factor data for vascular injury and immune response using electrochemiluminescence ELISA. Samples have been distributed to collaborating scientists for additional assays. Rigorous consideration of sample quality and assay sensitivity, specificity and precision have provided confidence in the assays that will be used in the next cycle. The Biomarker Core is comprised of a seasoned group of translational laboratory investigators with extensive experience in molecular neurosciences and neuropathology, neurology, psychiatry, and biorepository management. The Biomarker Core will work with the Clinical Core to continue optimal collection and on-site processing procedures for blood and CSF, bank and distribute biofluids, and generate ATN and modifying factor data using the most sensitive and reliable methods available. In order to bridge plasma with CSF and better understand the potential of blood biomarkers of brain health, we will generate data in simultaneously collected plasma and CSF in HABS and affiliated samples. Based on preliminary data and Project interests, in the next Cycle, the Biomarker Core will measure Ab42, NT1 tau and NfL, vascular injury markers (especially VEGF-related molecules) and Th1 and Th2 inflammatory markers (e.g., IFN-g and IL-4 respectively) and other associated markers. It will also continue to identify, evaluate and implement novel technologies and biomarkers for HABS. Data generated will be quality-controlled and transferred to DataCentral in coordination with the Analytic Core for use in Projects 1-4.
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会议论文
EFFECTS OF STRESS, ALLOSTATIC LOAD, AND SOCIAL INEQUITIES ON BRAIN STRUCTURE, FUNCTION, AND COGNITION IN THE EARLY-TO-MIDLIFE TRANSITION
  • 批准号:
    10283068
  • 项目类别:
  • 资助金额:
    $17.57万
  • 财政年份:
    2021
  • 负责人:
    STEVEN E ARNOLD
  • 依托单位:
EFFECTS OF STRESS, ALLOSTATIC LOAD, AND SOCIAL INEQUITIES ON BRAIN STRUCTURE, FUNCTION, AND COGNITION IN THE EARLY-TO-MIDLIFE TRANSITION
  • 批准号:
    10673901
  • 项目类别:
  • 资助金额:
    $17.6万
  • 财政年份:
    2021
  • 负责人:
    STEVEN E ARNOLD
  • 依托单位:
Biomarker Core
  • 批准号:
    10620683
  • 项目类别:
  • 资助金额:
    $30.19万
  • 财政年份:
    2019
  • 负责人:
    STEVEN E ARNOLD
  • 依托单位:
Biomarker Core
  • 批准号:
    10378619
  • 项目类别:
  • 资助金额:
    $30.19万
  • 财政年份:
    2019
  • 负责人:
    STEVEN E ARNOLD
  • 依托单位:
海外基金