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Risk factors for FEV(1) decline in mild COPD and high-risk populations

BACKGROUND: Early diagnosis of COPD is often not achieved due to limited recognition and limited access to the pulmonary function test. Our hypothesis was that lung function decline may be different between populations with mild COPD and those who are at high risk and do not receive treatment. PATIE...

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Autores principales: Chen, Shujing, Wang, Changhui, Li, Bing, Shi, Guochao, Li, Huiping, Zhang, Jing, Gu, Yutong, Zhou, Jian, Song, Yuanlin, Bai, Chunxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291456/
https://www.ncbi.nlm.nih.gov/pubmed/28184155
http://dx.doi.org/10.2147/COPD.S118106
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author Chen, Shujing
Wang, Changhui
Li, Bing
Shi, Guochao
Li, Huiping
Zhang, Jing
Gu, Yutong
Zhou, Jian
Song, Yuanlin
Bai, Chunxue
author_facet Chen, Shujing
Wang, Changhui
Li, Bing
Shi, Guochao
Li, Huiping
Zhang, Jing
Gu, Yutong
Zhou, Jian
Song, Yuanlin
Bai, Chunxue
author_sort Chen, Shujing
collection PubMed
description BACKGROUND: Early diagnosis of COPD is often not achieved due to limited recognition and limited access to the pulmonary function test. Our hypothesis was that lung function decline may be different between populations with mild COPD and those who are at high risk and do not receive treatment. PATIENTS AND METHODS: Subjects with mild COPD and those from a high-risk COPD population were recruited from a community-based COPD epidemiological study after obtaining consent. Baseline clinical characteristics, symptom questionnaire, spirometry, low-dose computed tomography (LDCT) chest scan, and blood plasma biomarker data were collected initially and then 1 year later. RESULTS: A total of 617 participants were recruited, and 438 eventually completed the first-year follow-up visit; 72 participants (46 males) were in the mild COPD group, and 225 participants (165 males) were in the high-risk group. The mean forced expiratory volume in the first second of expiration (FEV(1)) decline in the mild COPD group was 129 mL, which was significantly higher than the 30 mL decline in the high-risk population group (P=0.005). Group category (odds ratio [OR] =0.230) and COPD Assessment Test (CAT) score (OR =9.912) were independent risk factors for an FEV(1)% predicted decline of >15% for all participants. In the mild COPD group, patients with a higher CAT (OR =5.310) and Emphysema Index (OR =5.681) were associated with a FEV(1)% predicted decline of >15% at the first-year follow-up. No factor showed a significantly predictive effect on FEV(1) decline in the high-risk COPD group. CONCLUSION: Group category was an independent influential factor associated with FEV(1) decline.
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spelling pubmed-52914562017-02-09 Risk factors for FEV(1) decline in mild COPD and high-risk populations Chen, Shujing Wang, Changhui Li, Bing Shi, Guochao Li, Huiping Zhang, Jing Gu, Yutong Zhou, Jian Song, Yuanlin Bai, Chunxue Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Early diagnosis of COPD is often not achieved due to limited recognition and limited access to the pulmonary function test. Our hypothesis was that lung function decline may be different between populations with mild COPD and those who are at high risk and do not receive treatment. PATIENTS AND METHODS: Subjects with mild COPD and those from a high-risk COPD population were recruited from a community-based COPD epidemiological study after obtaining consent. Baseline clinical characteristics, symptom questionnaire, spirometry, low-dose computed tomography (LDCT) chest scan, and blood plasma biomarker data were collected initially and then 1 year later. RESULTS: A total of 617 participants were recruited, and 438 eventually completed the first-year follow-up visit; 72 participants (46 males) were in the mild COPD group, and 225 participants (165 males) were in the high-risk group. The mean forced expiratory volume in the first second of expiration (FEV(1)) decline in the mild COPD group was 129 mL, which was significantly higher than the 30 mL decline in the high-risk population group (P=0.005). Group category (odds ratio [OR] =0.230) and COPD Assessment Test (CAT) score (OR =9.912) were independent risk factors for an FEV(1)% predicted decline of >15% for all participants. In the mild COPD group, patients with a higher CAT (OR =5.310) and Emphysema Index (OR =5.681) were associated with a FEV(1)% predicted decline of >15% at the first-year follow-up. No factor showed a significantly predictive effect on FEV(1) decline in the high-risk COPD group. CONCLUSION: Group category was an independent influential factor associated with FEV(1) decline. Dove Medical Press 2017-01-27 /pmc/articles/PMC5291456/ /pubmed/28184155 http://dx.doi.org/10.2147/COPD.S118106 Text en © 2017 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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
Chen, Shujing
Wang, Changhui
Li, Bing
Shi, Guochao
Li, Huiping
Zhang, Jing
Gu, Yutong
Zhou, Jian
Song, Yuanlin
Bai, Chunxue
Risk factors for FEV(1) decline in mild COPD and high-risk populations
title Risk factors for FEV(1) decline in mild COPD and high-risk populations
title_full Risk factors for FEV(1) decline in mild COPD and high-risk populations
title_fullStr Risk factors for FEV(1) decline in mild COPD and high-risk populations
title_full_unstemmed Risk factors for FEV(1) decline in mild COPD and high-risk populations
title_short Risk factors for FEV(1) decline in mild COPD and high-risk populations
title_sort risk factors for fev(1) decline in mild copd and high-risk populations
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291456/
https://www.ncbi.nlm.nih.gov/pubmed/28184155
http://dx.doi.org/10.2147/COPD.S118106
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