Imaging tau, amyloid, and neurodegeneration in PPA
Imaging tau, amyloid, and neurodegeneration in PPA
批准号:
9176694
负责人:
BRADFORD C DICKERSON
金额:
$85.5万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-01 至 2021-08-31
关键词:
AddressAffinityAlzheimer&aposs DiseaseAmyloidAnatomyAphasiaAtrophicBindingBiological MarkersBrainBrain regionCerebrospinal FluidClassificationClinicalClinical ResearchClinical TrialsCountryDataDementiaDevelopmentDiagnosisDiagnosticDiagnostic SpecificityDiseaseEnrollmentFaceFrontotemporal Lobar DegenerationsGoalsImageImaging TechniquesIndividualKineticsLanguageLigandsLiquid substanceMagnetic Resonance ImagingMeasuresMethodsMolecular DiagnosisMonitorMultimodal ImagingNerve DegenerationNeurodegenerative DisordersOutcome MeasureParticipantPathologyPatient MonitoringPatientsPatternPositron-Emission TomographyPrimary Progressive AphasiaPropertyRecruitment ActivitySamplingScanningSignal TransductionSpatial DistributionSymptomsSyndromeTechnologyTemporal LobeTestingTracerTranslatingValidity and ReliabilityWorkabstractingaccurate diagnosisamyloid imagingamyloid pathologybasecerebral atrophyclinical careclinical phenotypecognitive functioncohortdesigneffective therapyfluorodeoxyglucose positron emission tomographyfrontal lobeimaging biomarkerimaging modalityimprovedin vivolanguage impairmentmolecular pathologymolecular targeted therapiesnext generationnoveltau Proteinstetrahydrobiopterintool
中文摘要
摘要
原发性进行性失语(PPA)是一种破坏性的神经退行性综合征
这涉及到失语症的持续发展,而其他认知能力相对较差
函数,至少在其过程的早期是这样。有多个子类型,也有多个
潜在的病理。PPA及其子类型可能很难与其他
神经退行性疾病和相互之间,特别是在他们的过程早期。
目前几乎没有临床工具来辅助PPA和PPA的早期特异性诊断
它的子类型。
我们最近在以下方面取得了实质性的初步进展
新的成像技术在早期特异性诊断中可能非常有价值
PPA背后特定病理的分子基础。我们建议使用tau和
淀粉样蛋白成像示踪剂试图区分这些潜在的分子
病理、FDG-PET、功能连接性MRI和形态结构
MRI测量和纵向监测神经退行性变的标志物
语言网络(S)等脑区。除了更准确的诊断外,
这些措施可能对预测和监测下降和
推定疗法的效果。
这项提案的总体目标是将这些方法从新的科学
技术转化为临床有用的工具,可供全国各地的临床医生使用
并在国际上提高诊断特异度和评估能力
PPA及其亚型。
英文摘要
Abstract
Primary progressive aphasia (PPA) is a devastating neurodegenerative syndrome
that involves relentless development of aphasia with relative sparing of other cognitive
functions, at least early in its course. There are multiple subtypes as well as multiple
underlying pathologies. PPA and its subtypes can be difficult to differentiate from other
neurodegenerative disorders and from each other, particularly early in their course.
There are currently few clinical tools to assist in the early specific diagnosis of PPA and
its subtypes.
We have recently made substantial preliminary progress toward the development of
novel imaging techniques that could be extremely valuable in early specific diagnosis of
the molecular basis of specific pathologies underlying PPA. We propose to use tau and
amyloid imaging tracers to attempt to discriminate these underlying molecular
pathologies, and FDG-PET, functional connectivity MRI, and morphometric structural
MRI to measure and longitudinally monitor markers of neurodegeneration in the
language network(s) and other brain regions. In addition to more accurate diagnosis,
these measures will likely be important for prognostication and monitoring of decline and
the effects of putative therapies.
The overall goal of this proposal is to translate these methods from new scientific
technologies into clinically useful tools that can be used by clinicians around the country
and internationally to improve the diagnostic specificity and assessment capabilities for
PPA and its subtypes.
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