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The World of Dementia Beyond 2020

Identifieur interne : 006311 ( Main/Exploration ); précédent : 006310; suivant : 006312

The World of Dementia Beyond 2020

Auteurs : Henry Brodaty [Belgique] ; Monique M. B. Breteler [Belgique] ; Steven T. Dekosky [Belgique] ; Pascale Dorenlot [Belgique] ; Laura Fratiglioni [Belgique] ; Christoph Hock [Belgique] ; Paul-Ariel Kenigsberg [Belgique] ; Philip Scheltens [Belgique] ; Bart De Strooper [Belgique]

Source :

RBID : ISTEX:3532435BFD3EF646FC74FD62B25CB9AE4AC6283F

Descripteurs français

English descriptors

Abstract

Counterpoised against dire projections of the tripling of the prevalence of dementia over the next 40 years are major developments in diagnostic biomarkers, neuroimaging, the molecular biology of Alzheimer's disease (AD), epidemiology of risk and protective factors, and drug treatments—mainly targeting the amyloid pathway, tau protein, and immunotherapy—that may have the potential to modify the progression of AD. Drug combinations and presymptomatic treatments are also being investigated. Previous trials of dementia‐modifying drugs have not shown benefit, and even if current Phase III trials prove successful, these drugs will not eradicate other dementias, could (if not curative) increase dementia duration and prevalence, and are unlikely to come onto the market before 2020. In the meantime, delaying the onset of dementia by even 2 years would have significant economic and societal effects. This article provides an overview of current achievements and potentials of basic and clinical research that might affect the development of dementia prevalence and care within the near future.

Url:
DOI: 10.1111/j.1532-5415.2011.03365.x


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title level="j" type="main">Journal of the American Geriatrics Society</title>
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<term>Adverse effects</term>
<term>Alzheimer</term>
<term>Alzheimer disease</term>
<term>Alzheimers dement</term>
<term>Amyloid</term>
<term>Amyloid pathway</term>
<term>Amyloid precursor protein</term>
<term>Apoe</term>
<term>Clinical effect phase</term>
<term>Clinical trials</term>
<term>Consulting fees</term>
<term>Current phase</term>
<term>Dementia</term>
<term>Dementia prevalence</term>
<term>Deposition inhibitor</term>
<term>Diabetes mellitus</term>
<term>Diagnosis</term>
<term>Dire projections</term>
<term>Drug development</term>
<term>Drug therapies</term>
<term>Elderly</term>
<term>Fondation</term>
<term>Fondation mederic alzheimer</term>
<term>Geriatrics</term>
<term>Gerontology</term>
<term>Global burden</term>
<term>Glycogen synthase</term>
<term>Henry brodaty</term>
<term>Immunization</term>
<term>Immunotherapy</term>
<term>Inhibitor</term>
<term>Lancet neurol</term>
<term>Late life</term>
<term>Literature searches</term>
<term>Medical research council</term>
<term>Molecular biology</term>
<term>Nancial relationships</term>
<term>Nerve growth factor</term>
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<term>Passive immunotherapy</term>
<term>Peptide</term>
<term>Pharmaceutical industry</term>
<term>Pparg stimulant</term>
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<term>Protein antibody</term>
<term>Public health</term>
<term>Receptor</term>
<term>Research centre</term>
<term>Scientific research</term>
<term>Societal costs</term>
<term>Study phase</term>
<term>Synthesis inhibitor</term>
<term>Treatment</term>
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<term>World</term>
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<term>Amyloid pathway</term>
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<term>Clinical effect phase</term>
<term>Clinical trials</term>
<term>Consulting fees</term>
<term>Current phase</term>
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<div type="abstract" xml:lang="en">Counterpoised against dire projections of the tripling of the prevalence of dementia over the next 40 years are major developments in diagnostic biomarkers, neuroimaging, the molecular biology of Alzheimer's disease (AD), epidemiology of risk and protective factors, and drug treatments—mainly targeting the amyloid pathway, tau protein, and immunotherapy—that may have the potential to modify the progression of AD. Drug combinations and presymptomatic treatments are also being investigated. Previous trials of dementia‐modifying drugs have not shown benefit, and even if current Phase III trials prove successful, these drugs will not eradicate other dementias, could (if not curative) increase dementia duration and prevalence, and are unlikely to come onto the market before 2020. In the meantime, delaying the onset of dementia by even 2 years would have significant economic and societal effects. This article provides an overview of current achievements and potentials of basic and clinical research that might affect the development of dementia prevalence and care within the near future.</div>
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