Movement Disorders (revue)

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Defining At-Risk Populations for Parkinson's Disease: Lessons From Ongoing Studies

Identifieur interne : 002B12 ( PascalFrancis/Curation ); précédent : 002B11; suivant : 002B13

Defining At-Risk Populations for Parkinson's Disease: Lessons From Ongoing Studies

Auteurs : Daniela Berg [Allemagne] ; Ken Marek [États-Unis] ; George W. Ross [États-Unis] ; Werner Poewe [Autriche]

Source :

RBID : Pascal:12-0223365

Descripteurs français

English descriptors

Abstract

It is currently widely acknowledged that the natural history of PD includes a preclinical phase, and there are increasing efforts to identify markers that would allow the identification of individuals at risk for PD. Here, we discuss the issues related to defining at-risk populations for PD and review findings of current population-based cohorts that have reported potential biomarkers for PD, such as the Honolulu-Asia Aging Study (HAAS) and the PRIPS (Prospective Validation of Risk factors for the development of Parkinson Syndromes) study. We also discuss enriched risk cohorts designed to evaluate specificity and predictive value of markers exemplified by the PARS (Parkinson Associated Risk Study) and the TREND (Tubinger evaluation of Risk factors for the Early detection of NeuroDegeneration) study. Although there is still a long way to go, studies designed according to these concepts might eventually provide sufficient data to form the basis for future screening programs for PD risk to be applied at a population level.
pA  
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A08 01  1  ENG  @1 Defining At-Risk Populations for Parkinson's Disease: Lessons From Ongoing Studies
A09 01  1  ENG  @1 Prodromal Parkinson's Disease
A11 01  1    @1 BERG (Daniela)
A11 02  1    @1 MAREK (Ken)
A11 03  1    @1 ROSS (George W.)
A11 04  1    @1 POEWE (Werner)
A12 01  1    @1 BERG (Daniela) @9 ed.
A12 02  1    @1 POEWE (Werner) @9 ed.
A14 01      @1 Department of Neurodegeneration, Hertie Institute of Clinical Brain Research and German Center of Neurodegenerative Diseases, University of Tübingen @2 Tübingen @3 DEU @Z 1 aut.
A14 02      @1 Institute for Neurodegenerative Disorders @2 New Haven, Connecticut @3 USA @Z 2 aut.
A14 03      @1 VA Pacific Islands Health Care System, Honolulu, Hawaii, USA, and Kuakini Medical Center @2 Honolulu, Hawaii @3 USA @Z 3 aut.
A14 04      @1 Department of Neurology, University of Innsbruck @2 Innsbruck @3 AUT @Z 4 aut.
A15 01      @1 Department of Neurodegeneration, Hertie Institute of Clinical Brain Research and German Center of Neurodegenerative Diseases (DZNE), University of Tübingen @2 Tübingen @3 DEU @Z 1 aut.
A15 02      @1 Department of Neurology, University of Innsbruck @2 Innsbruck @3 AUT @Z 2 aut.
A20       @1 656-665
A21       @1 2012
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C01 01    ENG  @0 It is currently widely acknowledged that the natural history of PD includes a preclinical phase, and there are increasing efforts to identify markers that would allow the identification of individuals at risk for PD. Here, we discuss the issues related to defining at-risk populations for PD and review findings of current population-based cohorts that have reported potential biomarkers for PD, such as the Honolulu-Asia Aging Study (HAAS) and the PRIPS (Prospective Validation of Risk factors for the development of Parkinson Syndromes) study. We also discuss enriched risk cohorts designed to evaluate specificity and predictive value of markers exemplified by the PARS (Parkinson Associated Risk Study) and the TREND (Tubinger evaluation of Risk factors for the Early detection of NeuroDegeneration) study. Although there is still a long way to go, studies designed according to these concepts might eventually provide sufficient data to form the basis for future screening programs for PD risk to be applied at a population level.
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C03 01  X  FRE  @0 Maladie de Parkinson @2 NM @5 01
C03 01  X  ENG  @0 Parkinson disease @2 NM @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @2 NM @5 01
C03 02  X  FRE  @0 Pathologie du système nerveux @5 02
C03 02  X  ENG  @0 Nervous system diseases @5 02
C03 02  X  SPA  @0 Sistema nervioso patología @5 02
C03 03  X  FRE  @0 Facteur risque @5 09
C03 03  X  ENG  @0 Risk factor @5 09
C03 03  X  SPA  @0 Factor riesgo @5 09
C03 04  X  FRE  @0 Asymptomatique @5 10
C03 04  X  ENG  @0 Asymptomatic @5 10
C03 04  X  SPA  @0 Asintomático @5 10
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Pathologie du système nerveux central @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
N21       @1 170
N44 01      @1 OTO
N82       @1 OTO

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Pascal:12-0223365

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