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Advances in Alzheimer’s Disease Drug Development

Alzheimer’s disease (AD) is the foremost cause of dementia worldwide. Clinically, AD manifests as progressive memory impairment followed by a gradual decline in other cognitive abilities leading to complete functional dependency. Recent biomarker studies indicate that AD is characterized by a long a...

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Detalles Bibliográficos
Autores principales: Rafii, Michael S, Aisen, Paul S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373002/
https://www.ncbi.nlm.nih.gov/pubmed/25857341
http://dx.doi.org/10.1186/s12916-015-0297-4
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author Rafii, Michael S
Aisen, Paul S
author_facet Rafii, Michael S
Aisen, Paul S
author_sort Rafii, Michael S
collection PubMed
description Alzheimer’s disease (AD) is the foremost cause of dementia worldwide. Clinically, AD manifests as progressive memory impairment followed by a gradual decline in other cognitive abilities leading to complete functional dependency. Recent biomarker studies indicate that AD is characterized by a long asymptomatic phase, with the development of pathology occurring at least a decade prior to the onset of any symptoms. Current FDA-approved treatments target neurotransmitter abnormalities associated with the disease but do not affect what is believed to be the underlying etiology. In this review, we briefly discuss the most recent therapeutic strategies being employed in AD clinical trials, as well the scientific rationale with which they have been developed.
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spelling pubmed-43730022015-03-26 Advances in Alzheimer’s Disease Drug Development Rafii, Michael S Aisen, Paul S BMC Med Minireview Alzheimer’s disease (AD) is the foremost cause of dementia worldwide. Clinically, AD manifests as progressive memory impairment followed by a gradual decline in other cognitive abilities leading to complete functional dependency. Recent biomarker studies indicate that AD is characterized by a long asymptomatic phase, with the development of pathology occurring at least a decade prior to the onset of any symptoms. Current FDA-approved treatments target neurotransmitter abnormalities associated with the disease but do not affect what is believed to be the underlying etiology. In this review, we briefly discuss the most recent therapeutic strategies being employed in AD clinical trials, as well the scientific rationale with which they have been developed. BioMed Central 2015-03-25 /pmc/articles/PMC4373002/ /pubmed/25857341 http://dx.doi.org/10.1186/s12916-015-0297-4 Text en © Rafii and Aisen; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Minireview
Rafii, Michael S
Aisen, Paul S
Advances in Alzheimer’s Disease Drug Development
title Advances in Alzheimer’s Disease Drug Development
title_full Advances in Alzheimer’s Disease Drug Development
title_fullStr Advances in Alzheimer’s Disease Drug Development
title_full_unstemmed Advances in Alzheimer’s Disease Drug Development
title_short Advances in Alzheimer’s Disease Drug Development
title_sort advances in alzheimer’s disease drug development
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373002/
https://www.ncbi.nlm.nih.gov/pubmed/25857341
http://dx.doi.org/10.1186/s12916-015-0297-4
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