grant

Biomarkers and Risk Factors for Prodromal Parkinson's Disease and its Progression

Organization HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTHLocation BOSTON, UNITED STATESPosted 1 Apr 2022Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY20252-Phenyl-Benzopyrans2-Phenyl-Chromenes2019 novel corona virus2019 novel coronavirus2019-nCoV21+ years oldActive Follow-upAddressAdrenergic beta-AntagonistsAdrenergic beta-BlockersAdultAdult HumanAgonistAllelism TestAntigensAppearanceBiologicalBiological MarkersBrainBrain Nervous SystemCOVID-19COVID-19 affectedCOVID-19 consequenceCOVID-19 effectCOVID-19 impactCOVID-19 impactedCOVID-19 virusCOVID19 virusCV-19CaffeineCarnitineClinicalCoV-2CoV2Complementation TestConstipationCoronavirus Infectious Disease 2019DataDiagnosisDietary PracticesDisability preventionDiseaseDisease ProgressionDisorderDrugsDyskinesia SyndromesEarly InterventionEarly identificationEncephalonEventFlavonoidsFollow-Up StudiesFollowup StudiesFoodFundingFutureGenetic Complementation TestGoalsHealth Care ProfessionalHealth ProfessionalHeterogeneityIndividualIntermediary MetabolismInterventionInvestigationKnowledgeLifeLife StyleLifestyleLipidsMachine LearningMedical HistoryMedicationMetabolic ProcessesMetabolismMonitorMotorMovement Disorder SyndromesMovement DisordersNINDSNational Institute of Neurological Diseases and StrokeNational Institute of Neurological Disorders and StrokeNatural HistoryNerve DegenerationNeuron DegenerationNurses' Health StudyNutrientParalysis AgitansParkinsonParkinson DiseaseParkinsonianParkinsonian ConditionParkinsonian DiseasesParkinsonian DisordersParkinsonian SyndromeParkinsonismParticipantPatientsPersonal Medical HistoryPersonal Medical History EpidemiologyPharmaceutical PreparationsPhasePhysical activityPlayPopulationPositionPositioning AttributePreventing disabilitiesPrevention trialPrimary ParkinsonismProbabilityREM Behavior DisorderREM Sleep Behavior DisorderRapid Eye Movement Behavior DisorderRapid Eye Movement Sleep Behavior DisorderRecommendationResearchResearch ResourcesResourcesRisk FactorsRoleSARS corona virus 2SARS-CO-V2SARS-COVID-2SARS-CoV-2SARS-CoV2SARS-associated corona virus 2SARS-associated coronavirus 2SARS-coronavirus-2SARS-related corona virus 2SARS-related coronavirus 2SARSCoV2SamplingSebumSebumsSevere Acute Respiratory Coronavirus 2Severe Acute Respiratory Distress Syndrome CoV 2Severe Acute Respiratory Distress Syndrome Corona Virus 2Severe Acute Respiratory Distress Syndrome Coronavirus 2Severe Acute Respiratory Syndrome CoV 2Severe Acute Respiratory Syndrome-associated coronavirus 2Severe Acute Respiratory Syndrome-related coronavirus 2Severe acute respiratory syndrome associated corona virus 2Severe acute respiratory syndrome coronavirus 2Severe acute respiratory syndrome related corona virus 2SmokingSocietiesSourceSphingolipidsSubgroupSurvey InstrumentSurveysTestingTimeTrainingTrans TestVolatilizationWomanWomen's cohortWuhan coronavirusactive followupadulthoodalgorithm trainingbeta blockerbeta-Adrenergic Blocking Agentsbeta-Adrenergic Receptor Blockadersbio-markersbiologicbiologic markerbiomarkercase controlcase-controlledcohortcohort in womencohort on womencomplementation analysiscomplementation approachcoronavirus disease 2019coronavirus disease 2019 consequencecoronavirus disease 2019 effectcoronavirus disease 2019 impactcoronavirus disease 2019 viruscoronavirus disease-19coronavirus disease-19 impactcoronavirus disease-19 viruscoronavirus infectious disease-19designdesigningdietarydietary patterndisease riskdisorder riskdrug/agentexperiencefemale cohortfollow upfollow-upfollowed upfollowuphCoV19hyposmiaimmunogeninsightmachine based learningmalleable riskmenmetabolomemetabonomemodifiable risknCoV2neural degenerationneurodegenerationneurodegenerativeneurological degenerationneuronal degenerationnew markernovelnovel biomarkernovel markerprediction algorithmprospectiverecruitreduced smellscreeningscreeningssexsocial rolevirtual
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Full Description

PROJECT SUMMARY The highest priority recommended by NINDS for clinical Parkinson’s research is
to define “the features and natural history of prodromal Parkinson disease (PPD), including the events

that underlie phenoconversion to clinically manifest PD, and biomarkers or other determinants of

prodromal subtypes with the goal of providing sufficient rationale to initiate proof-of-concept prevention

trials....” We are in a privileged position to address this priority by leveraging 25 years of research on

PD in the Nurses’ Health Study (NHS) and the Health Professionals Follow-up Study (HPFS), large

cohorts of women and men recruited in mid-adult life and followed prospectively for over 30 years. In

2012, we screened the active participants in these cohorts for probable REM sleep behavior disorder

(pRBD) and constipation, and selected a sub-cohort enriched for these features for further investigation

(the ProPD cohort). This sub-cohort included 20,455 individuals who have so far completed two

olfactory tests and two comprehensive mailed surveys of non-motor and early motor features of PPD,

and have been actively followed until 2018. We are now proposing to extend the longitudinal follow-up

of this unique cohort and its source population to monitor the progression of prodromal features and

phenoconversion to clinically manifest PD (“phenoconversion”, for brevity), thus providing important

insights on the course of PPD and fill the gap between current knowledge and what we need to know

for implementing prevention trials. Further, as part of the proposed project, we will examine the impact

of covid-19 on PPD and its progression and collect new biological samples to evaluate the sebum

volatilome and metabolome, novel promising and non-invasive biomarkers that could play an important

role in the early identification of PPD. The Aims of the study include: i) to obtain an in-depth descriptive

characterization of PPD and its heterogeneity; ii) to identify risk factors for PPD progression and

phenoconversion; iii) to assess the impact of SARS-Cov2/covid-19 on features of prodromal PD and

phenoconversion; and iv) to evaluate the relationship between the sebum volatilome and metabolome

with prodromal features and manifest PD (sebum samples will be collected from individuals with high

probability of PPD, manifest PD, and matched controls). A unique and virtually irreproducible strength

of the proposed study are the data prospectively collected since mid-adult life (men were 40 to 65 at

recruitment, women 30 to 55) on lifestyle and medical history, including risk factors for PD and several

features associated with PPD. If funded, the proposed study stands to lead to groundbreaking

discoveries and create an invaluable resource that will offer numerous opportunities for further in-depth

investigations on PPD and its determinants. Most importantly, the information generated by the

proposed investigation will be pivotal to assess the feasibility of prevention trials and inform their design.

Grant Number: 5R01NS126260-04
NIH Institute/Center: NIH

Principal Investigator: ALBERTO ASCHERIO

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