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The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System

OBJECTIVE: Osteoporosis, which is now recognized as a major comorbidity of chronic obstructive pulmonary disease (COPD), must be diagnosed by appropriate methods. The aims of this study were to clarify the relationships between bone mineral density (BMD) and COPD-related clinical variables and to ex...

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Autores principales: Sakurai-Iesato, Yoriko, Kawata, Naoko, Tada, Yuji, Iesato, Ken, Matsuura, Yukiko, Yahaba, Misuzu, Suzuki, Toshio, Ikari, Jun, Yanagawa, Noriyuki, Kasahara, Yasunori, West, James, Tatsumi, Koichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548669/
https://www.ncbi.nlm.nih.gov/pubmed/28717072
http://dx.doi.org/10.2169/internalmedicine.56.6910
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author Sakurai-Iesato, Yoriko
Kawata, Naoko
Tada, Yuji
Iesato, Ken
Matsuura, Yukiko
Yahaba, Misuzu
Suzuki, Toshio
Ikari, Jun
Yanagawa, Noriyuki
Kasahara, Yasunori
West, James
Tatsumi, Koichiro
author_facet Sakurai-Iesato, Yoriko
Kawata, Naoko
Tada, Yuji
Iesato, Ken
Matsuura, Yukiko
Yahaba, Misuzu
Suzuki, Toshio
Ikari, Jun
Yanagawa, Noriyuki
Kasahara, Yasunori
West, James
Tatsumi, Koichiro
author_sort Sakurai-Iesato, Yoriko
collection PubMed
description OBJECTIVE: Osteoporosis, which is now recognized as a major comorbidity of chronic obstructive pulmonary disease (COPD), must be diagnosed by appropriate methods. The aims of this study were to clarify the relationships between bone mineral density (BMD) and COPD-related clinical variables and to explore the association of BMD with the updated Global Initiative for Chronic Obstructive Lung Disease (GOLD) classification in men. METHODS: We enrolled 50 Japanese men with clinically stable COPD who underwent dual-energy X-ray absorptiometry (DEXA), pulmonary function testing, and computerized tomography (CT) and who had completed a questionnaire (COPD assessment test [CAT]). We determined the association between the T-score and other tested parameters and compared the BMD of patients in each GOLD category. RESULTS: Twenty-three of the 50 patients (46.0%) were diagnosed with osteopenia, and 7 (14.0%) were diagnosed with osteoporosis. The BMD findings were significantly correlated with the CAT score, forced expiratory volume in 1 second percentage predicted (FEV(1)% predicted), low attenuation volume percentage (LAV%), and percentage of cross-sectional area of small pulmonary vessels (%CSA) on CT images. Notably, the median T-score of the GOLD category D participants was significantly lower than that of the participants in each of the other categories (A [-0.98], B [-1.06], C [-1.05], and D [-2.19], p<0.05). CONCLUSION: Reduced BMD was associated with airflow limitation, extent of radiographic findings, and a poor quality of life (QOL) in patients with COPD. The BMD of GOLD category D patients was the lowest of all of the patients evaluated, and category D patients may benefit from active intervention for osteoporosis.
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spelling pubmed-55486692017-08-11 The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System Sakurai-Iesato, Yoriko Kawata, Naoko Tada, Yuji Iesato, Ken Matsuura, Yukiko Yahaba, Misuzu Suzuki, Toshio Ikari, Jun Yanagawa, Noriyuki Kasahara, Yasunori West, James Tatsumi, Koichiro Intern Med Original Article OBJECTIVE: Osteoporosis, which is now recognized as a major comorbidity of chronic obstructive pulmonary disease (COPD), must be diagnosed by appropriate methods. The aims of this study were to clarify the relationships between bone mineral density (BMD) and COPD-related clinical variables and to explore the association of BMD with the updated Global Initiative for Chronic Obstructive Lung Disease (GOLD) classification in men. METHODS: We enrolled 50 Japanese men with clinically stable COPD who underwent dual-energy X-ray absorptiometry (DEXA), pulmonary function testing, and computerized tomography (CT) and who had completed a questionnaire (COPD assessment test [CAT]). We determined the association between the T-score and other tested parameters and compared the BMD of patients in each GOLD category. RESULTS: Twenty-three of the 50 patients (46.0%) were diagnosed with osteopenia, and 7 (14.0%) were diagnosed with osteoporosis. The BMD findings were significantly correlated with the CAT score, forced expiratory volume in 1 second percentage predicted (FEV(1)% predicted), low attenuation volume percentage (LAV%), and percentage of cross-sectional area of small pulmonary vessels (%CSA) on CT images. Notably, the median T-score of the GOLD category D participants was significantly lower than that of the participants in each of the other categories (A [-0.98], B [-1.06], C [-1.05], and D [-2.19], p<0.05). CONCLUSION: Reduced BMD was associated with airflow limitation, extent of radiographic findings, and a poor quality of life (QOL) in patients with COPD. The BMD of GOLD category D patients was the lowest of all of the patients evaluated, and category D patients may benefit from active intervention for osteoporosis. The Japanese Society of Internal Medicine 2017-07-15 /pmc/articles/PMC5548669/ /pubmed/28717072 http://dx.doi.org/10.2169/internalmedicine.56.6910 Text en Copyright © 2017 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Sakurai-Iesato, Yoriko
Kawata, Naoko
Tada, Yuji
Iesato, Ken
Matsuura, Yukiko
Yahaba, Misuzu
Suzuki, Toshio
Ikari, Jun
Yanagawa, Noriyuki
Kasahara, Yasunori
West, James
Tatsumi, Koichiro
The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title_full The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title_fullStr The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title_full_unstemmed The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title_short The Relationship of Bone Mineral Density in Men with Chronic Obstructive Pulmonary Disease Classified According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Combined Chronic Obstructive Pulmonary Disease (COPD) Assessment System
title_sort relationship of bone mineral density in men with chronic obstructive pulmonary disease classified according to the global initiative for chronic obstructive lung disease (gold) combined chronic obstructive pulmonary disease (copd) assessment system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548669/
https://www.ncbi.nlm.nih.gov/pubmed/28717072
http://dx.doi.org/10.2169/internalmedicine.56.6910
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