Advanced signal processing methods for neural data analysis to support development of brain dynamic biomarkers for research and clinical applications in patients with Alzheimer's and related dementias
Advanced signal processing methods for neural data analysis to support development of brain dynamic biomarkers for research and clinical applications in patients with Alzheimer's and related dementias
批准号:
10739673
负责人:
Patrick L. Purdon
金额:
$130.38万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-01 至 2028-05-31
关键词:
AlgorithmsAlzheimer&aposs DiseaseAlzheimer&aposs disease pathologyAlzheimer&aposs disease patientAlzheimer&aposs disease related dementiaAlzheimer’s disease biomarkerAmyloidAmyloid beta-ProteinArticulationBiological MarkersBrainClinicalClinical TrialsCognitiveCommunitiesDataData AnalysesDevelopmentDevice or Instrument DevelopmentDigital biomarkerDisease ProgressionEP300 geneEarly DiagnosisElderlyElectroencephalographyError SourcesEvent-Related PotentialsFrequenciesGoalsIndividualMagnetic Resonance ImagingMarkov ChainsMeasurementMeasuresMethodsModelingMorphologic artifactsNational Institute on AgingNerve DegenerationNeurobehavioral ManifestationsNoisePharmaceutical PreparationsPhasePopulationResearchRestSignal TransductionSleepSoftware ToolsSourceSpace ModelsStructureTechnologyTherapeuticThickTimeVariantbiomarker developmentclinical applicationcognitive performancedesigndigital technologyimprovedinnovationinsightinterestlearning algorithmneuralneuroimaging markerneurophysiologyneurotransmissionnon rapid eye movementnovelresponsesignal processingsource localizationspatial relationshiptask analysistau Proteinstool
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Digital technologies can have enormous impact in the prediction, early detection, and tracking of Alzheimer’s
disease progression. In particular, there is a need to develop digital biomarkers that can detect early changes in
brain function before the onset of cognitive symptoms and/or brain biomarkers. The EEG is a compelling
candidate for an early “digital biomarker” of AD as numerous EEG features are known to be correlated with AD
progression and fundamental biomarkers. Unfortunately, there is limited evidence that these same EEG
measures, as currently constructed to describe population-level data, can accurately track, or predict AD
progression in individuals. One reason for this is that EEG signals have many sources of with- and between-
subject variation that are not accounted for in current analysis methods, leading to imprecise markers that only
have sufficient statistical power at the population-level. There have been recent advances in neural signal
processing that make it possible to account for these sources of error and in turn dramatically improve the
precision of EEG-derived measures. Over the past several years our lab has made significant strides to account
for these sources of error leading us to develop novel, sophisticated signal processing algorithms that can
enhance the precision of EEG derived measures. Through the specific aims of this project, we seek to provide
the AD research community with a suite of powerful, accessible signal processing software tools that will
dramatically enhance the precision and quality of EEG-derived biomarkers related to AD progression.
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会议论文
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