Metabolomics and risk of Parkinson's Disease
Metabolomics and risk of Parkinson's Disease
批准号:
9313961
负责人:
ALBERTO ASCHERIO
金额:
$56.31万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-01 至 2020-06-30
关键词:
AffectAgeAlanineAmericanArchivesBiological MarkersBloodBlood specimenBranched-Chain Amino AcidsCaffeineCancer Prevention Study IICholineChronicChronic DiseaseClinicalCoffeeCohort StudiesConfounding Factors (Epidemiology)ConsumptionControlled StudyCreatineCross-Sectional StudiesDataData CollectionDiabetes MellitusDiagnosisDiagnosticDietDiseaseDisease ProgressionEarly DiagnosisEarly identificationEtiologyEventFailureFollow-Up StudiesFunctional disorderFundingGlutamatesGoalsHealth ProfessionalIncidenceIndividualInstitutesInsulin ResistanceInvestigationLife StyleMachine LearningMeasuresMediatingMedicalMedical HistoryMetabolicMetabolic PathwayMethodsMotorNational Institute of Neurological Disorders and StrokeNatureNerve DegenerationNeurodegenerative DisordersNurses&apos Health StudyParkinson DiseaseParticipantPatientsPersonsPhasePhysical activityPlasmaPopulationProgressive DiseaseResearchResourcesRiskRisk FactorsSamplingSmokingSpecificityTechniquesTherapeuticTimeUnited StatesUnited States National Institutes of HealthUpdateUrateValidationWomen&aposs Health NursingWorkacylcarnitineaging populationbasebrain cellcancer preventioncase controlcigarette smokingclinical Diagnosiscohortdesigndiabetes riskdisabilitydisorder riskfollow-upgender differenceinsightinterestmenmetabolic profilemetabolomemetabolomicsmitochondrial dysfunctionmotor symptomneuron lossnovelnovel strategiesnutritionperipheral bloodpre-clinicalprospectivepublic health relevancesexspecific biomarkerstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Parkinson disease (PD) is the second most common neurodegenerative disease in the United States and affects over one million Americans; this number is growing due to population aging. Current treatments do not prevent the disease progression that ultimately results in severe disability. There is thus a compelling need to develop neuroprotective treatments. Because at the time of the clinical diagnosis of PD there is already substantial neuronal loss, such treatments should ideally be initiated earlier. Aims of the
proposed investigation are to implement and validate a novel metabolomic approach for the identification of early changes in peripheral blood of individuals with preclinical or premotor PD.
The metabolomic results will be integrated with detailed and validated information on risk factors for PD, which has been collected prospectively and periodically updated. We expect by this means to identify new clues to the etiology of PD and to identify a metabolomic signature of PD that could contribute to an early diagnosis. To achieve these goals, we will take advantage of data and blood samples collected from over 80,000 participants in three large ongoing cohorts, the Nurses' Health Study (NHS), the Health Professional Follow-up Study (HPFS), and the Cancer Prevention Study-II Nutrition, who have been followed for over 25 years for incident Parkinson disease. We expect to include a total of 805 incident cases of PD that will be matched to 805 controls, using a nested case-control design.
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