PIB PET Scanning in Speech and Language Based Dementias
PIB PET Scanning in Speech and Language Based Dementias
批准号:
8606353
负责人:
Keith A Josephs
金额:
$35.16万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-02-01 至 2016-01-31
关键词:
6-hydroxybenzothiazoleActivities of Daily LivingAlgorithmsAlzheimer&aposs DiseaseAmyloid beta-ProteinAmyloid depositionAnomiaAreaAtrophicAutopsyBehavioralBiological MarkersBrainCenter for Translational Science ActivitiesClinicClinicalComprehensionDataDementiaDepositionDetectionDevelopmentDiagnosisDiscipline of Nuclear MedicineDiseaseDoctor of PhilosophyEquipmentExecutive DysfunctionFoundationsFrontotemporal Lobar DegenerationsFunctional disorderFutureGlucoseGoalsGoldGrantImageImaging TechniquesImpairmentJointsLaboratoriesLanguageLanguage DisordersLeadLimb structureMagnetic Resonance ImagingManuscriptsMedical centerMemoryMemory LossMethodsMinorityMovement DisordersNeurodegenerative DisordersNeurologicNeurologyNeuropsychological TestsNeurosciencesNuclearParietal LobeParkinsonian DisordersPathologyPatientsPeer ReviewPittsburgh Compound-BPositioning AttributePositron-Emission TomographyPrimary Progressive AphasiaPrincipal InvestigatorPrizeProductionProteinsPublicationsPublishingRadiology SpecialtyRecruitment ActivityResearchResearch PersonnelRestScanningScientistSeveritiesSolidSolutionsSpecialistSpeechSpeech DisordersSpeech PathologistSpeech PathologyTechniquesTestingTrainingUnited StatesVisuospatialWorkamyloid imagingaphasicbasebeta amyloid pathologycost effectivediagnosis evaluationexecutive functionexpectationexperiencefrontal lobegray matterin vivoinnovationnervous system disorderneuropsychologicalpublic health relevanceradiologisttomography
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Speech and language based dementias (SLDs) (often referred to as primary progressive aphasias) are neurodegenerative diseases in which speech and language impairments are the most salient features of the disease and explain deficits in activities of daily living. These dementias may or may not be associated with the deposition of the protein beta-amyloid in the brain, which until recently could only be determined at postmortem. Since new treatments will likely target underlying abnormal proteins, accurate prediction of the pathology underlying the SLDs is critical. The recent development of amyloid imaging compounds now allows the in vivo detection of beta-amyloid in the brain. Unfortunately, amyloid imaging compounds are expensive and are not accessible to most medical centers throughout the United States. The objectives of the studies outlined in this proposal are to identify clinical, neuropsychological or non-amyloid imaging biomarkers that are readily available, relatively inexpensive, and non-invasive, that will allow the prediction of beta-amyloid in the brain in patients with SLDs. To accomplish this goal we will be using the amyloid imaging compound 11C Pittsburgh Compound B (PiB) as the gold standard for the detection of beta-amyloid. The methods will include detailed neurological, speech and language and neuropsychological assessments, magnetic resonance imaging, and [18-F]-fluoro-deoxy-glucose (FDG) and PiB PET scanning. Associations between PiB positive scanning and these techniques will be sought. One of the most salient features of the speech and language assessments will be the determination of the presence and severity of apraxia of speech and its association with beta-amyloid deposition. This study will be carried out at the Mayo Clinic in Rochester, MN, which evaluates a large number of patients with SLDs annually. The study also intends to recruit minorities with SLDs which are currently understudied. The methods will be performed by a team of world renowned scientists including dementia, movement disorders and speech pathology specialists, radiology researchers, a nuclear medicine scientist, neuropsychologists, and biostatisticians. The long term goal of our research is to develop a cost effective algorithmic approach to the evaluation and diagnosis of patients with SLDs.
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DOI:
10.1016/j.nicl.2022.102999
发表时间:
2022
期刊:
NeuroImage. Clinical
影响因子:
--
作者:
[Valls Carbo A, Reid RI, Tosakulwong N, Weigand SD, Duffy JR, Clark HM, Utianski RL, Botha H, Machulda MM, Strand EA, Schwarz CG, Jack CR, Josephs KA, Whitwell JL]
通讯作者:
Whitwell JL
DOI:
10.1111/ene.12331
发表时间:
2014-07
期刊:
European journal of neurology
影响因子:
5.1
作者:
[Jung Y, Whitwell JL, Duffy JR, Strand EA, Machulda MM, Senjem ML, Lowe V, Jack CR Jr, Josephs KA]
通讯作者:
Josephs KA
Prominent auditory deficits in primary progressive aphasia: A case study.
原发性进行性失语症的显着听觉缺陷:案例研究。
DOI:
10.1016/j.cortex.2019.01.021
发表时间:
2019
期刊:
Cortex; a journal devoted to the study of the nervous system and behavior
影响因子:
--
作者:
[Utianski,ReneL, Duffy,JosephR, Clark,HeatherM, Machulda,MaryM, Dickson,DennisW, Whitwell,JenniferL, Josephs,KeithA]
通讯作者:
Josephs,KeithA
Word Fluency Test Performance in Primary Progressive Aphasia and Primary Progressive Apraxia of Speech.
原发性进行性失语症和原发性进行性言语失用症的单词流利度测试表现。
DOI:
10.1044/2021_ajslp-21-00058
发表时间:
2021
期刊:
American journal of speech-language pathology
影响因子:
2.6
作者:
[Scheffel,Lucia, Duffy,JosephR, Strand,EdytheA, Josephs,KeithA]
通讯作者:
Josephs,KeithA
DOI:
10.1111/ene.12271
发表时间:
2014-03
期刊:
European journal of neurology
影响因子:
5.1
作者:
[Clark HM, Duffy JR, Whitwell JL, Ahlskog JE, Sorenson EJ, Josephs KA]
通讯作者:
Josephs KA
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资助金额:$23.02万
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财政年份:2016
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Longitudinal multi-modal imaging in progressive supranuclear palsy syndromes
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批准号:10468193
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资助金额:$77.93万
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财政年份:2015
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Longitudinal Multi-modal Imaging in Progressive Supranuclear Palsy Syndromes
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资助金额:$78.45万
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批准号:9894894
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项目类别:
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资助金额:$76.33万
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财政年份:2015
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依托单位:
Longitudinal multi-modal imaging in progressive supranuclear palsy syndromes
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批准号:10266026
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资助金额:$77.93万
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Understanding the role of TDP-43 in Alzheimer's disease and FTLD
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资助金额:$32.49万
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Understanding the role of TDP-43 in Alzheimers disease and FTLD
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Understanding the role of TDP-43 in Alzheimer’s disease and FTLD
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PIB PET Scanning in Speech and Language Based Dementias
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依托单位:
海外基金