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
项目摘要
帕金森病(PD)是仅次于阿尔茨海默病的第二大常见神经退行性疾病,
也是导致65岁以上人群残疾的主要原因。PD属于一系列疾病,
“突触核蛋白病”,定义为不溶性突触α-突触核蛋白的进行性聚集,包括
其他疾病如多系统萎缩和路易体痴呆。目前,还没有客观的测试
可以用来明确诊断帕金森病此外,突触核蛋白病的鉴别诊断是非常重要的。
具有挑战性,并严重依赖于医生的临床评估。该领域的一个关键目标是可靠地识别
突触核蛋白病在疾病的早期,无症状阶段,以允许最好的机会,正确的疾病
修改或预防性治疗才有效。该提案旨在开发一种小分子荧光
视网膜造影剂作为PD和其他相关突触核蛋白病的新诊断剂。
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