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Authors Chen SJ, Wang CH, Li B, Shi GC, Li HP, Zhang J, Gu YT, Zhou J, Song YL, Bai CX
Received 26 July 2016
Accepted for publication 31 October 2016
Published 27 January 2017 Volume 2017:12 Pages 435—442
DOI https://doi.org/10.2147/COPD.S118106
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Professor Hsiao-Chi Chuang
Peer reviewer comments 2
Editor who approved publication: Dr Richard Russell
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 (FEV1) 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 FEV1% 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 FEV1% predicted decline of >15% at the first-year
follow-up. No factor showed a significantly predictive effect on FEV1 decline
in the high-risk COPD group.
Conclusion: Group category was an independent influential factor
associated with FEV1 decline.
Keywords: COPD, biomarker, lung function
decline, Emphysema Index, spirometry