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Osteoporosis Associated with Chronic Obstructive Pulmonary Disease
Recent epidemiological studies have revealed that osteoporosis is closely associated with common chronic diseases including diabetes, hypertension, chronic kidney disorders, and chronic obstructive pulmonary disease (COPD). COPD is a chronic inflammatory airway disease but now well known to be assoc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Bone and Mineral Research
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018603/ https://www.ncbi.nlm.nih.gov/pubmed/27622174 http://dx.doi.org/10.11005/jbm.2016.23.3.111 |
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author | Okazaki, Ryo Watanabe, Reiko Inoue, Daisuke |
author_facet | Okazaki, Ryo Watanabe, Reiko Inoue, Daisuke |
author_sort | Okazaki, Ryo |
collection | PubMed |
description | Recent epidemiological studies have revealed that osteoporosis is closely associated with common chronic diseases including diabetes, hypertension, chronic kidney disorders, and chronic obstructive pulmonary disease (COPD). COPD is a chronic inflammatory airway disease but now well known to be associated with various systemic comorbidities including osteoporosis. Osteoporosis and osteoporotic fractures are extremely common in COPD patients, which have significant impacts on their quality of life (QOL), activities of daily life (ADL), respiratory function, and possibly their prognosis. COPD-associated osteoporosis is however extremely under-recognized, hence undertreated. Recent studies have suggested that both decreased bone mineral density (BMD) and impaired bone quality compromise bone strength causing fractures in COPD. In COPD patients, various general clinical risk factors for osteoporosis are present including smoking, older age, low body weight, and physical inactivity. In addition, disease-related risk factors such as decreased pulmonary function, inflammation, glucocorticoid use and vitamin D deficiency/insufficiency have been linked to the development of osteoporosis in COPD. Increased awareness of osteoporosis in COPD, especially that of high prevalence of vertebral fractures is called upon among general physicians as well as pulmonologists. Routine screening for osteoporosis and risk assessment of fractures will enable physicians to diagnose COPD patients with comorbid osteoporosis at an early stage. Timely prevention of developing osteoporosis together with appropriate treatment of established osteoporosis may improve QOL and ADL of the COPD patients, preserve their lung function and eventually result in better prognosis in these patients. |
format | Online Article Text |
id | pubmed-5018603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society for Bone and Mineral Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-50186032016-09-12 Osteoporosis Associated with Chronic Obstructive Pulmonary Disease Okazaki, Ryo Watanabe, Reiko Inoue, Daisuke J Bone Metab Review Article Recent epidemiological studies have revealed that osteoporosis is closely associated with common chronic diseases including diabetes, hypertension, chronic kidney disorders, and chronic obstructive pulmonary disease (COPD). COPD is a chronic inflammatory airway disease but now well known to be associated with various systemic comorbidities including osteoporosis. Osteoporosis and osteoporotic fractures are extremely common in COPD patients, which have significant impacts on their quality of life (QOL), activities of daily life (ADL), respiratory function, and possibly their prognosis. COPD-associated osteoporosis is however extremely under-recognized, hence undertreated. Recent studies have suggested that both decreased bone mineral density (BMD) and impaired bone quality compromise bone strength causing fractures in COPD. In COPD patients, various general clinical risk factors for osteoporosis are present including smoking, older age, low body weight, and physical inactivity. In addition, disease-related risk factors such as decreased pulmonary function, inflammation, glucocorticoid use and vitamin D deficiency/insufficiency have been linked to the development of osteoporosis in COPD. Increased awareness of osteoporosis in COPD, especially that of high prevalence of vertebral fractures is called upon among general physicians as well as pulmonologists. Routine screening for osteoporosis and risk assessment of fractures will enable physicians to diagnose COPD patients with comorbid osteoporosis at an early stage. Timely prevention of developing osteoporosis together with appropriate treatment of established osteoporosis may improve QOL and ADL of the COPD patients, preserve their lung function and eventually result in better prognosis in these patients. The Korean Society for Bone and Mineral Research 2016-08 2016-08-31 /pmc/articles/PMC5018603/ /pubmed/27622174 http://dx.doi.org/10.11005/jbm.2016.23.3.111 Text en Copyright © 2016 The Korean Society for Bone and Mineral Research http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Okazaki, Ryo Watanabe, Reiko Inoue, Daisuke Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title | Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title_full | Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title_fullStr | Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title_full_unstemmed | Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title_short | Osteoporosis Associated with Chronic Obstructive Pulmonary Disease |
title_sort | osteoporosis associated with chronic obstructive pulmonary disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018603/ https://www.ncbi.nlm.nih.gov/pubmed/27622174 http://dx.doi.org/10.11005/jbm.2016.23.3.111 |
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