Biomarkers and risk factors for prodromal Parkinson's disease and its progression
帕金森病前驱期及其进展的生物标志物和危险因素
基本信息
- 批准号:10594036
- 负责人:
- 金额:$ 47.7万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-04-01 至 2027-03-31
- 项目状态:未结题
- 来源:
- 关键词:2019-nCoVAddressAdrenergic beta-AntagonistsAdultAgonistAntigensAppearanceBiologicalBiological MarkersBrainCOVID-19COVID-19 impactCaffeineCarnitineClinicalConstipationDataDiagnosisDietary PracticesDisease ProgressionEarly InterventionEarly identificationEventFlavonoidsFollow-Up StudiesFoodFundingFutureGenetic Complementation TestGoalsHealth ProfessionalHeterogeneityIndividualInterventionInvestigationKnowledgeLifeLife StyleLipidsMachine LearningMedical HistoryMetabolismMonitorMotorMovement DisordersNational Institute of Neurological Disorders and StrokeNatural HistoryNerve DegenerationNurses&apos Health StudyNutrientParkinson DiseaseParkinsonian DisordersParticipantPatientsPharmaceutical PreparationsPhasePhysical activityPlayPopulationPositioning AttributePrevention trialProbabilityREM Sleep Behavior DisorderRecommendationResearchResourcesRisk FactorsRoleSamplingSebumSmokingSocietiesSourceSphingolipidsSubgroupSurveysTestingTimeTrainingVolatilizationWomanalgorithm trainingcase controlcohortdesigndietarydisabilitydisorder riskexperiencefollow-uphyposmiainsightmenmetabolomemodifiable risknovelnovel markerprediction algorithmpreventprospectiverecruitscreeningsexvirtual
项目摘要
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.
NINDS推荐临床帕金森病研究的最高优先级是
项目成果
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{{ truncateString('ALBERTO ASCHERIO', 18)}}的其他基金
Biomarkers and risk factors for prodromal Parkinson's disease and its progression
帕金森病前驱期及其进展的生物标志物和危险因素
- 批准号:
10417436 - 财政年份:2022
- 资助金额:
$ 47.7万 - 项目类别:
Serological profiling of the human virome and ALS risk in a military population
军人人群中人类病毒组和 ALS 风险的血清学分析
- 批准号:
10252746 - 财政年份:2020
- 资助金额:
$ 47.7万 - 项目类别:
Serological profiling of the human virome and ALS risk in a military population
军人人群中人类病毒组和 ALS 风险的血清学分析
- 批准号:
10438144 - 财政年份:2020
- 资助金额:
$ 47.7万 - 项目类别:
Serological profiling of the human virome and ALS risk in a military population
军人人群中人类病毒组和 ALS 风险的血清学分析
- 批准号:
10117845 - 财政年份:2020
- 资助金额:
$ 47.7万 - 项目类别:
Prospective Study of Vitamin D and MS Risk in African Americans
非裔美国人维生素 D 和多发性硬化症风险的前瞻性研究
- 批准号:
10242084 - 财政年份:2018
- 资助金额:
$ 47.7万 - 项目类别:
Prospective study of vitamin D and MS risk in African Americans
非裔美国人维生素 D 和多发性硬化症风险的前瞻性研究
- 批准号:
10018657 - 财政年份:2018
- 资助金额:
$ 47.7万 - 项目类别:
Vitamin D, Epstein-Barr virus infection, and cigarette smoking and risk of multip
维生素 D、EB 病毒感染、吸烟和多发性肺疾病的风险
- 批准号:
8228025 - 财政年份:2011
- 资助金额:
$ 47.7万 - 项目类别:
Vitamin D, Epstein-Barr virus infection, and cigarette smoking and risk of multip
维生素 D、EB 病毒感染、吸烟和多发性肺疾病的风险
- 批准号:
8449146 - 财政年份:2011
- 资助金额:
$ 47.7万 - 项目类别:
Vitamin D, Epstein-Barr virus infection, and cigarette smoking and risk of multip
维生素 D、EB 病毒感染、吸烟和多发性肺疾病的风险
- 批准号:
8084442 - 财政年份:2011
- 资助金额:
$ 47.7万 - 项目类别:
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