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Modeling the impact of COPD on the brain
Previous studies have shown that COPD adversely affects distant organs and body systems, including the brain. This pilot study aims to model the relationships between respiratory insufficiency and domains related to brain function, including low mood, subtly impaired cognition, systemic inflammation...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629981/ https://www.ncbi.nlm.nih.gov/pubmed/18990971 |
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author | Borson, Soo Scanlan, James Friedman, Seth Zuhr, Elizabeth Fields, Julie Aylward, Elizabeth Mahurin, Rodney Richards, Todd Anzai, Yoshimi Yukawa, Michi Yeh, Shingshing |
author_facet | Borson, Soo Scanlan, James Friedman, Seth Zuhr, Elizabeth Fields, Julie Aylward, Elizabeth Mahurin, Rodney Richards, Todd Anzai, Yoshimi Yukawa, Michi Yeh, Shingshing |
author_sort | Borson, Soo |
collection | PubMed |
description | Previous studies have shown that COPD adversely affects distant organs and body systems, including the brain. This pilot study aims to model the relationships between respiratory insufficiency and domains related to brain function, including low mood, subtly impaired cognition, systemic inflammation, and brain structural and neurochemical abnormalities. Nine healthy controls were compared with 18 age- and education-matched medically stable COPD patients, half of whom were oxygen-dependent. Measures included depression, anxiety, cognition, health status, spirometry, oximetry at rest and during 6-minute walk, and resting plasma cytokines and soluble receptors, brain MRI, and MR spectroscopy in regions relevant to mood and cognition. ANOVA was used to compare controls with patients and with COPD subgroups (oxygen users [n = 9] and nonusers [n = 9]), and only variables showing group differences at p ≤ 0.05 were included in multiple regressions controlling for age, gender, and education to develop the final model. Controls and COPD patients differed significantly in global cognition and memory, mood, and soluble TNFR1 levels but not brain structural or neurochemical measures. Multiple regressions identified pathways linking disease severity with impaired performance on sensitive cognitive processing measures, mediated through oxygen dependence, and with systemic inflammation (TNFR1), related through poor 6-minute walk performance. Oxygen desaturation with activity was related to indicators of brain tissue damage (increased frontal choline, which in turn was associated with subcortical white matter attenuation). This empirically derived model provides a conceptual framework for future studies of clinical interventions to protect the brain in patients with COPD, such as earlier oxygen supplementation for patients with desaturation during everyday activities. |
format | Text |
id | pubmed-2629981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26299812009-05-04 Modeling the impact of COPD on the brain Borson, Soo Scanlan, James Friedman, Seth Zuhr, Elizabeth Fields, Julie Aylward, Elizabeth Mahurin, Rodney Richards, Todd Anzai, Yoshimi Yukawa, Michi Yeh, Shingshing Int J Chron Obstruct Pulmon Dis Original Research Previous studies have shown that COPD adversely affects distant organs and body systems, including the brain. This pilot study aims to model the relationships between respiratory insufficiency and domains related to brain function, including low mood, subtly impaired cognition, systemic inflammation, and brain structural and neurochemical abnormalities. Nine healthy controls were compared with 18 age- and education-matched medically stable COPD patients, half of whom were oxygen-dependent. Measures included depression, anxiety, cognition, health status, spirometry, oximetry at rest and during 6-minute walk, and resting plasma cytokines and soluble receptors, brain MRI, and MR spectroscopy in regions relevant to mood and cognition. ANOVA was used to compare controls with patients and with COPD subgroups (oxygen users [n = 9] and nonusers [n = 9]), and only variables showing group differences at p ≤ 0.05 were included in multiple regressions controlling for age, gender, and education to develop the final model. Controls and COPD patients differed significantly in global cognition and memory, mood, and soluble TNFR1 levels but not brain structural or neurochemical measures. Multiple regressions identified pathways linking disease severity with impaired performance on sensitive cognitive processing measures, mediated through oxygen dependence, and with systemic inflammation (TNFR1), related through poor 6-minute walk performance. Oxygen desaturation with activity was related to indicators of brain tissue damage (increased frontal choline, which in turn was associated with subcortical white matter attenuation). This empirically derived model provides a conceptual framework for future studies of clinical interventions to protect the brain in patients with COPD, such as earlier oxygen supplementation for patients with desaturation during everyday activities. Dove Medical Press 2008-09 2008-09 /pmc/articles/PMC2629981/ /pubmed/18990971 Text en © 2008 Dove Medical Press Limited. All rights reserved |
spellingShingle | Original Research Borson, Soo Scanlan, James Friedman, Seth Zuhr, Elizabeth Fields, Julie Aylward, Elizabeth Mahurin, Rodney Richards, Todd Anzai, Yoshimi Yukawa, Michi Yeh, Shingshing Modeling the impact of COPD on the brain |
title | Modeling the impact of COPD on the brain |
title_full | Modeling the impact of COPD on the brain |
title_fullStr | Modeling the impact of COPD on the brain |
title_full_unstemmed | Modeling the impact of COPD on the brain |
title_short | Modeling the impact of COPD on the brain |
title_sort | modeling the impact of copd on the brain |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629981/ https://www.ncbi.nlm.nih.gov/pubmed/18990971 |
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