课题基金 / 基金详情

Neural Correlates and Modifiers of Cognitive Aging

Neural Correlates and Modifiers of Cognitive Aging
认知衰老的神经相关因素和调节因素
批准号:
8080215
负责人:
NAFTALI RAZ
金额:
$55.23万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-09-30 至 2015-05-31
关键词:
AccelerationAcetylcholineAcuteAdultAdverse effectsAffectAgeAgingAging-Related ProcessAllelesAlzheimer&aposs DiseaseAmericanAnti-Inflammatory AgentsAnti-inflammatoryApoptosisAttentionAwardBiochemicalBiologicalBiological MarkersBiological ProcessBloodBlood GlucoseBlood PressureBlood VesselsBoxingBrainBrain regionBrain-Derived Neurotrophic FactorC-reactive proteinCardiacCatalytic DomainCell Differentiation processCell ProliferationCerebrumChromosomes, Human, Pair 2ChronicClinicalCognitionCognitiveCognitive agingCohort EffectCollectionCompensatory HyperinsulinemiaComplementComputer softwareCross-Sectional StudiesDataData AnalysesData SetDecelerationDesire for foodDeteriorationDiabetes MellitusDiffusionDiseaseDopamineElderlyEnsureEnzymesEpisodic memoryEvaluationExhibitsExperimental Diabetes MellitusFamilyGenesGeneticGenetic EpistasisGenetic PolymorphismGenetic RiskGenetic VariationGenomicsGenotypeGlucokinaseGlucoseGlucose-6-PhosphateGlycosylated HemoglobinGoalsGrowthHTR2A geneHealthHippocampus (Brain)HomocysteineHomocystineHomozygoteHospitalsHumanHyperglycemiaHypertensionImage AnalysisIndividualIndividual DifferencesInflammationInflammatoryInflammatory ResponseInstructionInsula of ReilInsulinInsulin ResistanceInterleukin-1Interleukin-13Interleukin-6InvestigationIronKAI1 geneKnockout MiceLengthLesionLettersLightLinkLiteratureLiverLocationLongitudinal StudiesMTHFR geneMagnetic Resonance ImagingMaintenanceManualsMeasurementMeasuresMemoryMetabolicMethodologyMethodsMissionModelingModificationMorbidity - disease rateMuscarinic Acetylcholine ReceptorMyelinNatureNeocortexNeurobiologyNeurotransmittersNicotinic ReceptorsOther GeneticsPancreasParticipantPatternPerformancePersonal SatisfactionPersonsPhasePhosphorylationPhysiologic pulsePhysiologicalPlayPopulationPredispositionPriceProcessProgress ReportsPropertyProteinsProxyPublishingPulse PressureRelative (related person)RelianceReportingResearchResourcesRiskRisk FactorsRoleSamplingSampling StudiesSerotoninShapesShort-Term MemorySiteSolutionsSpeedStimulusStructureSurfaceSystemTestingTimeTrainingUniversitiesVariantVascular DementiaVentricularVertebral columnWorkage effectage relatedaging brainarea striatabaseblood glucose regulationblood pressure regulationbrain shapebrain volumecalcium metabolismcardiovascular risk factorcaudate nucleuscholinergiccognitive changecohortcytokinedesigndiabetes riskexecutive functionfasting glucosefollow-upgenetic risk factorgenetic variantglucose metabolismglucose sensorglucose uptakeglucose-6-phosphataseglycemic controlhealthy aginghuman TCF7L2 proteinimprovedindexinginsightinstrumentinsulin sensitivityinterestiron metabolismlongitudinal analysismeetingsmembermetabolic abnormality assessmentneocorticalneuroimagingnormal agingpresynapticprocessing speedreceptorrelating to nervous systemresearch studyresponsesexskillssynaptogenesistrendway findingwhite matter

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中文摘要
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英文摘要
The goals of this continuing project are 1. Aim 1. To describe the course of differential brain aging vyith a focus on the best-case-scenario naturalistic study of successful aging. With that focus, the study will complement existing large-scale longitudinal investigations of typical geriatric samples. Our objective is to examine the closest approximation to successful physiological aging to be found in an unselected human population. 2. Aim 2, To gain insights into mechanisms of age-related differential brain shrinkage by examining changes in microstructure of the white matter and indirect indices of regional brain iron content. 3. Aim 3. To evaluate the links between age-related regional brain changes (volume, diffusion and magnetization properties, and iron content) and performance in three cognitive domains with known vulnerability to aging: episodic memory, executive functions, and speed of processing. 4. Aim 4. To examine the effect of vascular risk factors (physiological and genetic) as modifiers of brain and cognitive aging. We will continue our investigation into the effects of sub-clinical levels of vascular risk conveyed by elevated blood pressure, circulating cardiac risk factors (homocysteine, C-reactive protein), elevated insulin, and genetic variants associated with vascular and metabolic risk (MTHFR C677T, IL1-p C511T, BDNF Val66Met, ACE l/D, ApoEpound4, diabetes risk genes, and polymorphisms related to specific neurotransmitters - acetylcholine, serotonin, dopamine). Aim 5. Common to all listed aims is a longitudinal approach to study of biological and cognitive change with Latent Growth Curves models that allow estimation of the shape of the trajectories of aging. Aim 6. Methodological contributions. During the proposed extension award period, we plan to initiate several methodological investigations, in which we will compared manual volumetry and ROI-based evaluation of white matter integrity with various semi-automated methods, with a hope to improve those methods to the level comparable with the "golden standard."
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Hemodynamic predictors of brain and cognitive aging
  • 批准号:
    6829234
  • 项目类别:
  • 资助金额:
    $5.86万
  • 财政年份:
    2004
  • 负责人:
    NAFTALI RAZ
  • 依托单位:
Hemodynamic predictors of brain and cognitive aging
  • 批准号:
    6948478
  • 项目类别:
  • 资助金额:
    $5.96万
  • 财政年份:
    2004
  • 负责人:
    NAFTALI RAZ
  • 依托单位:
NEURAL CORRELATES OF AGE RELATED DIFFERENCES IN MEMORY
  • 批准号:
    6371803
  • 项目类别:
  • 资助金额:
    $5.67万
  • 财政年份:
    1993
  • 负责人:
    NAFTALI RAZ
  • 依托单位:
NEURAL CORRELATES OF AGE-RELATED DIFFERENCES IN MEMORY
  • 批准号:
    3123205
  • 项目类别:
  • 资助金额:
    $20.93万
  • 财政年份:
    1993
  • 负责人:
    NAFTALI RAZ
  • 依托单位:
海外基金