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Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults
Damage to brain structures which constitute the distributed neural network that integrates respiratory muscle and pulmonary functions, can impair adequate ventilation and its volitional control. We tested the hypothesis that the level of brain pathology in older adults is associated with declining r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612667/ https://www.ncbi.nlm.nih.gov/pubmed/26539108 http://dx.doi.org/10.3389/fnagi.2015.00197 |
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author | Buchman, Aron S. Yu, Lei Wilson, Robert S. Dawe, Robert J. VanderHorst, Veronique Schneider, Julie A. Bennett, David A. |
author_facet | Buchman, Aron S. Yu, Lei Wilson, Robert S. Dawe, Robert J. VanderHorst, Veronique Schneider, Julie A. Bennett, David A. |
author_sort | Buchman, Aron S. |
collection | PubMed |
description | Damage to brain structures which constitute the distributed neural network that integrates respiratory muscle and pulmonary functions, can impair adequate ventilation and its volitional control. We tested the hypothesis that the level of brain pathology in older adults is associated with declining respiratory function measured during life. 1,409 older adults had annual testing with spirometry (SPI) and respiratory muscle strength (RMS) based on maximal inspiratory and maximal expiratory pressures (MEPs). Those who died underwent structured brain autopsy. On average, during 5 years of follow-up, SPI and RMS showed progressive decline which was moderately correlated (ρ = 0.57, p < 0.001). Among decedents (N = 447), indices of brain neuropathologies showed differential associations with declining SPI and RMS. Nigral neuronal loss was associated with the person-specific decline in SPI (Estimate, −0.016 unit/year, S.E. 0.006, p = 0.009) and reduction of the slope variance was equal to 4%. By contrast, Alzheimer’s disease (AD) pathology (Estimate, −0.030 unit/year, S.E. 0.009, p < 0.001) and macroscopic infarcts (−0.033 unit/year, S.E., 0.011, p = 0.003) were associated with the person-specific decline in RMS and reduction of the slope variance was equal to 7%. These results suggest that brain pathology is associated with the rate of declining respiratory function in older adults. |
format | Online Article Text |
id | pubmed-4612667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46126672015-11-04 Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults Buchman, Aron S. Yu, Lei Wilson, Robert S. Dawe, Robert J. VanderHorst, Veronique Schneider, Julie A. Bennett, David A. Front Aging Neurosci Neuroscience Damage to brain structures which constitute the distributed neural network that integrates respiratory muscle and pulmonary functions, can impair adequate ventilation and its volitional control. We tested the hypothesis that the level of brain pathology in older adults is associated with declining respiratory function measured during life. 1,409 older adults had annual testing with spirometry (SPI) and respiratory muscle strength (RMS) based on maximal inspiratory and maximal expiratory pressures (MEPs). Those who died underwent structured brain autopsy. On average, during 5 years of follow-up, SPI and RMS showed progressive decline which was moderately correlated (ρ = 0.57, p < 0.001). Among decedents (N = 447), indices of brain neuropathologies showed differential associations with declining SPI and RMS. Nigral neuronal loss was associated with the person-specific decline in SPI (Estimate, −0.016 unit/year, S.E. 0.006, p = 0.009) and reduction of the slope variance was equal to 4%. By contrast, Alzheimer’s disease (AD) pathology (Estimate, −0.030 unit/year, S.E. 0.009, p < 0.001) and macroscopic infarcts (−0.033 unit/year, S.E., 0.011, p = 0.003) were associated with the person-specific decline in RMS and reduction of the slope variance was equal to 7%. These results suggest that brain pathology is associated with the rate of declining respiratory function in older adults. Frontiers Media S.A. 2015-10-21 /pmc/articles/PMC4612667/ /pubmed/26539108 http://dx.doi.org/10.3389/fnagi.2015.00197 Text en Copyright © 2015 Buchman, Yu, Wilson, Dawe, VanderHorst, Schneider and Bennett. 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 Buchman, Aron S. Yu, Lei Wilson, Robert S. Dawe, Robert J. VanderHorst, Veronique Schneider, Julie A. Bennett, David A. Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title | Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title_full | Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title_fullStr | Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title_full_unstemmed | Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title_short | Post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
title_sort | post-mortem brain pathology is related to declining respiratory function in community-dwelling older adults |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612667/ https://www.ncbi.nlm.nih.gov/pubmed/26539108 http://dx.doi.org/10.3389/fnagi.2015.00197 |
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