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Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease?
Individuals with pathological aging, a form of cerebral amyloidosis in older people, have widespread extracellular amyloid-beta (Aβ) senile plaque deposits in the setting of limited neurofibrillary tau pathology. Unlike the characteristic finding of antemortem cognitive impairment in Alzheimer’s dis...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055017/ https://www.ncbi.nlm.nih.gov/pubmed/25031637 http://dx.doi.org/10.1186/alzrt254 |
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author | Murray, Melissa E Dickson, Dennis W |
author_facet | Murray, Melissa E Dickson, Dennis W |
author_sort | Murray, Melissa E |
collection | PubMed |
description | Individuals with pathological aging, a form of cerebral amyloidosis in older people, have widespread extracellular amyloid-beta (Aβ) senile plaque deposits in the setting of limited neurofibrillary tau pathology. Unlike the characteristic finding of antemortem cognitive impairment in Alzheimer’s disease patients, individuals with pathological aging usually lack cognitive impairment despite similar Aβ senile plaque burdens. It has been hypothesized that protective or resistance factors may underlie pathological aging, thus minimizing or preventing deleterious effects on cognition. Despite increasing interest and recognition, a review of the literature remains challenging given the range of terms used to describe pathological aging. This debate briefly reviews neuropathologic and biochemical evidence that pathological aging individuals have resistance factors to Aβ plaque pathology. Additionally, we will discuss evidence of pathological aging as an intermediate between normal individuals and Alzheimer’s disease patients, and discuss protective or resistance factors against vascular disease and neurofibrillary pathology. Lastly, we will emphasize the need for longitudinal biomarker evidence using amyloid positron emission tomography, which will provide a better understanding of the kinetics of Aβ deposition in pathological aging. |
format | Online Article Text |
id | pubmed-4055017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40550172015-05-06 Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? Murray, Melissa E Dickson, Dennis W Alzheimers Res Ther Debate Individuals with pathological aging, a form of cerebral amyloidosis in older people, have widespread extracellular amyloid-beta (Aβ) senile plaque deposits in the setting of limited neurofibrillary tau pathology. Unlike the characteristic finding of antemortem cognitive impairment in Alzheimer’s disease patients, individuals with pathological aging usually lack cognitive impairment despite similar Aβ senile plaque burdens. It has been hypothesized that protective or resistance factors may underlie pathological aging, thus minimizing or preventing deleterious effects on cognition. Despite increasing interest and recognition, a review of the literature remains challenging given the range of terms used to describe pathological aging. This debate briefly reviews neuropathologic and biochemical evidence that pathological aging individuals have resistance factors to Aβ plaque pathology. Additionally, we will discuss evidence of pathological aging as an intermediate between normal individuals and Alzheimer’s disease patients, and discuss protective or resistance factors against vascular disease and neurofibrillary pathology. Lastly, we will emphasize the need for longitudinal biomarker evidence using amyloid positron emission tomography, which will provide a better understanding of the kinetics of Aβ deposition in pathological aging. BioMed Central 2014-05-06 /pmc/articles/PMC4055017/ /pubmed/25031637 http://dx.doi.org/10.1186/alzrt254 Text en Copyright © 2014 Murray and Dickson; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available 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 | Debate Murray, Melissa E Dickson, Dennis W Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title | Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title_full | Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title_fullStr | Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title_full_unstemmed | Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title_short | Is pathological aging a successful resistance against amyloid-beta or preclinical Alzheimer’s disease? |
title_sort | is pathological aging a successful resistance against amyloid-beta or preclinical alzheimer’s disease? |
topic | Debate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055017/ https://www.ncbi.nlm.nih.gov/pubmed/25031637 http://dx.doi.org/10.1186/alzrt254 |
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