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Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease

Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder, the development of which is regulated by several environmental and genetic risk factors. Two factors theorized to contribute to the initiation and/or progression of AD pathogenesis are age-related increases in inflammation and...

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Autores principales: Christensen, Amy, Pike, Christian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493396/
https://www.ncbi.nlm.nih.gov/pubmed/26217222
http://dx.doi.org/10.3389/fnagi.2015.00130
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author Christensen, Amy
Pike, Christian J.
author_facet Christensen, Amy
Pike, Christian J.
author_sort Christensen, Amy
collection PubMed
description Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder, the development of which is regulated by several environmental and genetic risk factors. Two factors theorized to contribute to the initiation and/or progression of AD pathogenesis are age-related increases in inflammation and obesity. These factors may be particularly problematic in women. The onset of menopause in mid-life elevates the vulnerability of women to AD, an increased risk that is likely associated with the depletion of estrogens. Menopause is also linked with an abundance of additional changes, including increased central adiposity and inflammation. Here, we review the current literature to explore the interactions between obesity, inflammation, menopause and AD.
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spelling pubmed-44933962015-07-27 Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease Christensen, Amy Pike, Christian J. Front Aging Neurosci Neuroscience Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder, the development of which is regulated by several environmental and genetic risk factors. Two factors theorized to contribute to the initiation and/or progression of AD pathogenesis are age-related increases in inflammation and obesity. These factors may be particularly problematic in women. The onset of menopause in mid-life elevates the vulnerability of women to AD, an increased risk that is likely associated with the depletion of estrogens. Menopause is also linked with an abundance of additional changes, including increased central adiposity and inflammation. Here, we review the current literature to explore the interactions between obesity, inflammation, menopause and AD. Frontiers Media S.A. 2015-07-07 /pmc/articles/PMC4493396/ /pubmed/26217222 http://dx.doi.org/10.3389/fnagi.2015.00130 Text en Copyright © 2015 Christensen and Pike. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Christensen, Amy
Pike, Christian J.
Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title_full Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title_fullStr Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title_full_unstemmed Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title_short Menopause, obesity and inflammation: interactive risk factors for Alzheimer’s disease
title_sort menopause, obesity and inflammation: interactive risk factors for alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493396/
https://www.ncbi.nlm.nih.gov/pubmed/26217222
http://dx.doi.org/10.3389/fnagi.2015.00130
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