Characterizing the evolution of Subjective Cognitive Decline in preclinical Alzheimer's disease
Characterizing the evolution of Subjective Cognitive Decline in preclinical Alzheimer's disease
批准号:
10532669
负责人:
Rebecca E Amariglio
金额:
$75.96万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-03-01 至 2024-11-30
关键词:
AgeAlzheimer disease preventionAlzheimer&aposs DiseaseAlzheimer&aposs disease pathologyAlzheimer’s disease biomarkerAmyloidAmyloid beta-ProteinAnxietyBiological MarkersCellular PhoneClinicClinicalCognitiveCommunitiesComplementComputersCross-Sectional StudiesDemographic ImpactDisease MarkerDisease ProgressionEarly DiagnosisEducationElderlyElectronicsEpisodic memoryEtiologyEvolutionFrequenciesGeneticGleanGoalsHippocampusHomeImpaired cognitionIndividualInferiorInvestigationKnowledgeMagnetic Resonance ImagingMeasuresMemoryMemory DisordersMethodsModelingMoodsNational Institute on Alcohol Abuse and AlcoholismNerve DegenerationNeurobehavioral ManifestationsNeuropsychological TestsNeuropsychologyParticipantPatient Self-ReportPatternPerformancePersonsPhasePittsburgh Compound-BPositron-Emission TomographyPreventionPrevention trialQuestionnairesReportingResearchSelf AssessmentSeveritiesSeverity of illnessSourceStandardizationSymptomsTabletsTemporal LobeTimeWhite Matter Hyperintensityaging brainamyloid imagingassociated symptomautosomal dominant Alzheimer&aposs diseasecarrier statusclinical diagnosisclinical predictorscognitive functioncognitive performancecognitive testingcohortcommon symptomdirect applicationentorhinal cortexexecutive functionhigh riskimprovedin vivonovel strategiespre-clinicalrecruitrisk predictionsextau Proteinstau aggregationtreatment effecttreatment responsetreatment strategy
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Project Summary
As Alzheimer's disease (AD) treatment strategies increasingly focus on prevention at the preclinical stage, a
corresponding effort to improve detection of early changes in cognitive function is urgently needed. Subjective
Cognitive Decline (SCD) provides a unique opportunity to identify emerging cognitive symptoms from the
person's own perspective that can complement neuropsychological assessment at the preclinical stage.
Furthermore, SCD has direct applications for AD prevention trials seeking to demonstrate treatment effects
that impact study participants' daily lives. We propose to recruit a new cohort of SCD individuals who report a
concern for recent, persistent changes in cognitive functioning. Individuals will be recruited from both the
community and the memory disorders clinics (n=100) and will be followed over the course of 3 years.
Specifically, we will capture high frequency SCD report (i.e., quarterly) that can be administered unsupervised
via personal electronic device (e.g., computer, smart phone, tablet). In this way, participants will be able to
complete assessments at-home, rather than coming to the clinic. SCD trajectories will be associated with other
markers of disease severity, including in vivo AD biomarkers longitudinally, amyloid (Pittsburgh Compound B-
PET) and tau (Flortaucipir-PET) and objective cognitive decline. The information gleaned from these
complementary methods will improve our ability to identify high risk participants more likely to decline and to
track clinically meaningful response to treatment.
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