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Cortisol, cytokines, and hippocampal volume interactions in the elderly
Separate bodies of literature report that elevated pro-inflammatory cytokines and cortisol negatively affect hippocampal structure and cognitive functioning, particularly in older adults. Although interactions between cytokines and cortisol occur through a variety of known mechanisms, few studies co...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079951/ https://www.ncbi.nlm.nih.gov/pubmed/25071562 http://dx.doi.org/10.3389/fnagi.2014.00153 |
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author | Sudheimer, Keith D. O'Hara, Ruth Spiegel, David Powers, Bevin Kraemer, Helena C. Neri, Eric Weiner, Michael Hardan, Antonio Hallmayer, Joachim Dhabhar, Firdaus S. |
author_facet | Sudheimer, Keith D. O'Hara, Ruth Spiegel, David Powers, Bevin Kraemer, Helena C. Neri, Eric Weiner, Michael Hardan, Antonio Hallmayer, Joachim Dhabhar, Firdaus S. |
author_sort | Sudheimer, Keith D. |
collection | PubMed |
description | Separate bodies of literature report that elevated pro-inflammatory cytokines and cortisol negatively affect hippocampal structure and cognitive functioning, particularly in older adults. Although interactions between cytokines and cortisol occur through a variety of known mechanisms, few studies consider how their interactions affect brain structure. In this preliminary study, we assess the impact of interactions between circulating levels of IL-1Beta, IL-6, IL-8, IL-10, IL-12, TNF-alpha, and waking cortisol on hippocampal volume. Twenty-eight community-dwelling older adults underwent blood draws for quantification of circulating cytokines and saliva collections to quantify the cortisol awakening response. Hippocampal volume measurements were made using structural magnetic resonance imaging. Elevated levels of waking cortisol in conjunction with higher concentrations of IL-6 and TNF-alpha were associated with smaller hippocampal volumes. In addition, independent of cortisol, higher levels of IL-1beta and TNF-alpha were also associated with smaller hippocampal volumes. These data provide preliminary evidence that higher cortisol, in conjunction with higher IL-6 and TNF-alpha, are associated with smaller hippocampal volume in older adults. We suggest that the dynamic balance between the hypothalamic-pituitary adrenal axis and inflammation processes may explain hippocampal volume reductions in older adults better than either set of measures do in isolation. |
format | Online Article Text |
id | pubmed-4079951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40799512014-07-28 Cortisol, cytokines, and hippocampal volume interactions in the elderly Sudheimer, Keith D. O'Hara, Ruth Spiegel, David Powers, Bevin Kraemer, Helena C. Neri, Eric Weiner, Michael Hardan, Antonio Hallmayer, Joachim Dhabhar, Firdaus S. Front Aging Neurosci Neuroscience Separate bodies of literature report that elevated pro-inflammatory cytokines and cortisol negatively affect hippocampal structure and cognitive functioning, particularly in older adults. Although interactions between cytokines and cortisol occur through a variety of known mechanisms, few studies consider how their interactions affect brain structure. In this preliminary study, we assess the impact of interactions between circulating levels of IL-1Beta, IL-6, IL-8, IL-10, IL-12, TNF-alpha, and waking cortisol on hippocampal volume. Twenty-eight community-dwelling older adults underwent blood draws for quantification of circulating cytokines and saliva collections to quantify the cortisol awakening response. Hippocampal volume measurements were made using structural magnetic resonance imaging. Elevated levels of waking cortisol in conjunction with higher concentrations of IL-6 and TNF-alpha were associated with smaller hippocampal volumes. In addition, independent of cortisol, higher levels of IL-1beta and TNF-alpha were also associated with smaller hippocampal volumes. These data provide preliminary evidence that higher cortisol, in conjunction with higher IL-6 and TNF-alpha, are associated with smaller hippocampal volume in older adults. We suggest that the dynamic balance between the hypothalamic-pituitary adrenal axis and inflammation processes may explain hippocampal volume reductions in older adults better than either set of measures do in isolation. Frontiers Media S.A. 2014-07-03 /pmc/articles/PMC4079951/ /pubmed/25071562 http://dx.doi.org/10.3389/fnagi.2014.00153 Text en Copyright © 2014 Sudheimer, O‘Hara, Spiegel, Powers, Kraemer, Neri, Weiner, Hardan, Hallmayer and Dhabhar. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or 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 Sudheimer, Keith D. O'Hara, Ruth Spiegel, David Powers, Bevin Kraemer, Helena C. Neri, Eric Weiner, Michael Hardan, Antonio Hallmayer, Joachim Dhabhar, Firdaus S. Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title | Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title_full | Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title_fullStr | Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title_full_unstemmed | Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title_short | Cortisol, cytokines, and hippocampal volume interactions in the elderly |
title_sort | cortisol, cytokines, and hippocampal volume interactions in the elderly |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079951/ https://www.ncbi.nlm.nih.gov/pubmed/25071562 http://dx.doi.org/10.3389/fnagi.2014.00153 |
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