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Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease
BACKGROUND: Osteoporosis is an important issue for patients with chronic obstructive pulmonary disease (COPD). Worse systemic inflammation and reduced exercise capacity have been reported in COPD patients with obstructive sleep apnea (OSA), implying that OSA may be an independent factor for osteopor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321657/ https://www.ncbi.nlm.nih.gov/pubmed/25673983 http://dx.doi.org/10.2147/COPD.S72099 |
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author | Wang, Tsai-Yu Lo, Yu-Lun Chou, Pai-Chien Chung, Fu-Tsai Lin, Shu-Min Lin, Ting-Yu Lin, Horng-Chyuan Wang, Chun-Hua Yu, Chih-Teng Kuo, Han-Pin |
author_facet | Wang, Tsai-Yu Lo, Yu-Lun Chou, Pai-Chien Chung, Fu-Tsai Lin, Shu-Min Lin, Ting-Yu Lin, Horng-Chyuan Wang, Chun-Hua Yu, Chih-Teng Kuo, Han-Pin |
author_sort | Wang, Tsai-Yu |
collection | PubMed |
description | BACKGROUND: Osteoporosis is an important issue for patients with chronic obstructive pulmonary disease (COPD). Worse systemic inflammation and reduced exercise capacity have been reported in COPD patients with obstructive sleep apnea (OSA), implying that OSA may be an independent factor for osteoporosis in COPD patients. METHODS: A total of 66 patients with bone mineral density (BMD) and polysomnography results from a previous COPD cohort (January 2008 to January 2013) were retrospectively enrolled. Clinical characteristics such as medication, pulmonary function, BMD, and results of polysomnography were analyzed. RESULTS: The BMD in those with OSA was significantly lower than in those without OSA (−1.99±1.63 versus −1.27±1.14, P=0.045). In univariate analysis, body mass index, forced expiratory volume in 1 second, percentage of predicted value, incremental shuttle walk test, apnea–hypopnea index, and oxygen desaturation index (ODI) were significantly associated with BMD. After multivariate linear regression analysis, the ODI was still an independent factor for BMD. In addition, smaller total lung capacity is significantly associated with higher ODI and lower BMD, which implies that lower BMD might cause severer OSA via decreased total lung capacity. CONCLUSION: OSA may be an independent factor for BMD in patients with COPD, which implies a possible vicious cycle takes place in these patients. |
format | Online Article Text |
id | pubmed-4321657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43216572015-02-11 Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease Wang, Tsai-Yu Lo, Yu-Lun Chou, Pai-Chien Chung, Fu-Tsai Lin, Shu-Min Lin, Ting-Yu Lin, Horng-Chyuan Wang, Chun-Hua Yu, Chih-Teng Kuo, Han-Pin Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Osteoporosis is an important issue for patients with chronic obstructive pulmonary disease (COPD). Worse systemic inflammation and reduced exercise capacity have been reported in COPD patients with obstructive sleep apnea (OSA), implying that OSA may be an independent factor for osteoporosis in COPD patients. METHODS: A total of 66 patients with bone mineral density (BMD) and polysomnography results from a previous COPD cohort (January 2008 to January 2013) were retrospectively enrolled. Clinical characteristics such as medication, pulmonary function, BMD, and results of polysomnography were analyzed. RESULTS: The BMD in those with OSA was significantly lower than in those without OSA (−1.99±1.63 versus −1.27±1.14, P=0.045). In univariate analysis, body mass index, forced expiratory volume in 1 second, percentage of predicted value, incremental shuttle walk test, apnea–hypopnea index, and oxygen desaturation index (ODI) were significantly associated with BMD. After multivariate linear regression analysis, the ODI was still an independent factor for BMD. In addition, smaller total lung capacity is significantly associated with higher ODI and lower BMD, which implies that lower BMD might cause severer OSA via decreased total lung capacity. CONCLUSION: OSA may be an independent factor for BMD in patients with COPD, which implies a possible vicious cycle takes place in these patients. Dove Medical Press 2015-01-29 /pmc/articles/PMC4321657/ /pubmed/25673983 http://dx.doi.org/10.2147/COPD.S72099 Text en © 2015 Wang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wang, Tsai-Yu Lo, Yu-Lun Chou, Pai-Chien Chung, Fu-Tsai Lin, Shu-Min Lin, Ting-Yu Lin, Horng-Chyuan Wang, Chun-Hua Yu, Chih-Teng Kuo, Han-Pin Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title | Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title_full | Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title_fullStr | Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title_full_unstemmed | Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title_short | Associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
title_sort | associated bone mineral density and obstructive sleep apnea in chronic obstructive pulmonary disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321657/ https://www.ncbi.nlm.nih.gov/pubmed/25673983 http://dx.doi.org/10.2147/COPD.S72099 |
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