Differential diagnosis of Parkinson's and multiple system atrophy in non-human primate models using a novel a-synuclein retinal contrast agent and AI-assisted analytics
Differential diagnosis of Parkinson's and multiple system atrophy in non-human primate models using a novel a-synuclein retinal contrast agent and AI-assisted analytics
批准号:
10323567
负责人:
Stella Sarraf
金额:
$207.76万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-23 至 2023-08-31
关键词:
3-DimensionalAge-YearsAlzheimer&aposs DiseaseAnimal ModelArtificial IntelligenceAutopsyBindingBrain InjuriesCadaverCaringClinicalClinical TrialsCognitiveComputer softwareContrast MediaDataDepositionDetectionDevelopmentDevicesDiagnosisDiagnosticDifferential DiagnosisDiseaseEarly InterventionElementsEyeFluorescenceFreeze DryingFundusGoalsHumanImageIndividualKilogramLeadLewy Body DementiaMapsMissionModelingMonitorMotorMultiple System AtrophyNeurodegenerative DisordersOptical Coherence TomographyParkinson DiseasePathologicPathologyPatientsPharmaceutical PreparationsPhysiciansPreventive treatmentResearchResolutionRetinaSpecialistStructureSymptomsTestingTherapeutic InterventionTimeTissuesToxicogeneticsToxicologyTracerVisualVisualizationWorkage relatedalpha synucleinbaseclinical practicedeep learning algorithmdesigndisabilitydisease diagnosisdopaminergic neuronfluorescence imaginggraphical user interfacein vivomouse modelneuropsychiatrynonhuman primatenovelnovel diagnosticsphototoxicologyprogramsresearch clinical testingretinal imagingsmall moleculesynucleinsynucleinopathythree dimensional structurethree-dimensional visualizationtranslation to humans
中文摘要
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英文摘要
Project Summary
Parkinson’s Disease (PD) is the second most common neurodegenerative disease after Alzheimer’s disease,
and a major cause of disability in individuals over 65 years of age. PD belongs to a spectrum of diseases termed
the “synucleinopathies”, defined by the progressive aggregation of insoluble fibrillary a-synuclein, and includes
other disorders such as multiple system atrophy and Lewy body dementia. Currently, there are no objective tests
that can be used to definitively diagnose PD. In addition, differential diagnosis of synucleinopathies is very
challenging and relies heavily on a physician's clinical evaluation. A critical goal in the field is to reliably identify
synucleinopathies at early, asymptomatic stages of the disease, to allow the best chance for correct disease
modifying or preventative treatments to be effective. This proposal aims to develop a small molecule fluorescent
retinal contrast agent as a novel diagnostic for PD and other related synucleinopathies.
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会议论文
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海外基金