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  5. FIZZ2 as a biomarker for acute exacerbation of chronic obstructive pulmonary disease
 
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FIZZ2 as a biomarker for acute exacerbation of chronic obstructive pulmonary disease
File(s)
FIZZ2 as a Biomarker for Acute Exacerbation of Chronic Obstructive Pulmonary Disease.docx (2.81 MB)
Accepted version
Author(s)
Zhou, Ying
Qiao, Yingying
Adcock, Ian M
Zhou, Jun
Yao, Xin
Type
Journal Article
Abstract
Purpose
Found in inflammatory zone 2 (FIZZ2) is associated with lung inflammation. The aim of the study was to investigate the expression and utility of FIZZ2 as a marker for chronic obstructive pulmonary disease (COPD).

Methods
Immunohistochemistry was used to detect the expression of FIZZ2 in COPD. The serum concentration of FIZZ2 was measured by enzyme-linked immunosorbent assay and the episodes of acute exacerbations of COPD (AECOPD) in the following year were recorded.

Results
FIZZ2 expression was elevated in bronchial epithelial cells (0.217 ± 0.021 vs 0.099 ± 0.010, p < 0.0001) and negatively correlated with the pulmonary function (FEV1/FVC%) (p = 0.0149) and positively correlated with the smoking index (p = 0.0241). Serum level of FIZZ2 in COPD were significantly higher than that in healthy controls (561.6 ± 70.71 vs 52.24 ± 20.52 pg/ml, p < 0.0001) and increased with the COPD severity. Serum levels of FIZZ2 negatively correlated with the pulmonary function [Forced Vital Capacity (FVC), Forced Expiratory Volume (FEV1), FEV1%, FEV1/FVC) (r =  − 0.3086, − 0.3529, − 0.3343, and − 0.2676, respectively, p = 0.0003, p < 0.0001, p < 0.0001, p = 0.0014). The expression of human serum FIZZ2 was positively correlated with the smoking index (r = 0.2749, p = 0.0015). There was a positive correlation between the FIZZ2 concentration and the frequency of AECOPD episodes in the following year (r = 0.7291, p < 0.0001).

Conclusion
FIZZ2 expression was elevated in patients with COPD and its serum concentration might be a potential biomarker for AECOPD.
Date Issued
2021-12
Date Acceptance
2021-09-20
Citation
Lung: an international journal on lungs, airways and breathing, 2021, 199 (6), pp.629-638
URI
http://hdl.handle.net/10044/1/113407
URL
https://link.springer.com/article/10.1007/s00408-021-00483-1
DOI
https://www.dx.doi.org/10.1007/s00408-021-00483-1
ISSN
0341-2040
Publisher
Springer
Start Page
629
End Page
638
Journal / Book Title
Lung: an international journal on lungs, airways and breathing
Volume
199
Issue
6
Copyright Statement
Copyright © 2021 Springer-Verlag. This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s00408-021-00483-1
Identifier
https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000710371000001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
Subjects
Acute exacerbation of chronic obstructive pulmonary disease
ALPHA
ASTHMA
Biomarker
CELLS
EXPRESSION
FIZZ2/RELM beta
INFLAMMATION
Life Sciences & Biomedicine
LUNG
MOLECULE-BETA
MURINE
PROTEIN
RESISTIN
Respiratory System
Science & Technology
Publication Status
Published
Date Publish Online
2021-10-22
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