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The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review
BACKGROUND: Many studies have found that YKL-40 may play an important pathogenic role in COPD. However, the results of these studies were inconsistent. Therefore, we performed a systematic review and meta-analysis to investigate the role of YKL-40 in COPD. METHODS: We performed a systematic literatu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796800/ https://www.ncbi.nlm.nih.gov/pubmed/29430175 http://dx.doi.org/10.2147/COPD.S152655 |
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author | Tong, Xiang Wang, Dongguang Liu, Sitong Ma, Yao Li, Zhenzhen Tian, Panwen Fan, Hong |
author_facet | Tong, Xiang Wang, Dongguang Liu, Sitong Ma, Yao Li, Zhenzhen Tian, Panwen Fan, Hong |
author_sort | Tong, Xiang |
collection | PubMed |
description | BACKGROUND: Many studies have found that YKL-40 may play an important pathogenic role in COPD. However, the results of these studies were inconsistent. Therefore, we performed a systematic review and meta-analysis to investigate the role of YKL-40 in COPD. METHODS: We performed a systematic literature search in many database and commercial internet search engines to identify studies involving the role of YKL-40 in patients with COPD. The standardized mean difference (SMD) and Fisher’s Z-value with its 95% confidence interval (CI) were used to investigate the effect sizes. RESULTS: A total of 15 eligible articles including 16 case–control/cohort groups were included in the meta-analysis. The results indicated that the serum YKL-40 levels in patients with COPD were significantly higher than those in healthy controls (SMD =1.58, 95% CI =0.68–2.49, P=0.001), and it was correlated with lung function (pooled r=−0.32; Z=−0.33; P<0.001). The results of subgroup analysis found that the serum YKL-40 levels were statistically different between the exacerbation group and the stable group in patients with COPD (SMD =1.55, 95% CI =0.81–2.30, P<0.001). Moreover, the results indicated that the sputum YKL-40 levels in patients with COPD were also significantly higher than those in healthy controls (SMD =0.70, 95% CI =0.10–1.30, P=0.022). CONCLUSION: The current study suggests that YKL-40 may be implicated in bronchial inflammation and remodeling in COPD and may be considered as a useful biomarker for COPD diagnosis and monitoring. |
format | Online Article Text |
id | pubmed-5796800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57968002018-02-09 The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review Tong, Xiang Wang, Dongguang Liu, Sitong Ma, Yao Li, Zhenzhen Tian, Panwen Fan, Hong Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Many studies have found that YKL-40 may play an important pathogenic role in COPD. However, the results of these studies were inconsistent. Therefore, we performed a systematic review and meta-analysis to investigate the role of YKL-40 in COPD. METHODS: We performed a systematic literature search in many database and commercial internet search engines to identify studies involving the role of YKL-40 in patients with COPD. The standardized mean difference (SMD) and Fisher’s Z-value with its 95% confidence interval (CI) were used to investigate the effect sizes. RESULTS: A total of 15 eligible articles including 16 case–control/cohort groups were included in the meta-analysis. The results indicated that the serum YKL-40 levels in patients with COPD were significantly higher than those in healthy controls (SMD =1.58, 95% CI =0.68–2.49, P=0.001), and it was correlated with lung function (pooled r=−0.32; Z=−0.33; P<0.001). The results of subgroup analysis found that the serum YKL-40 levels were statistically different between the exacerbation group and the stable group in patients with COPD (SMD =1.55, 95% CI =0.81–2.30, P<0.001). Moreover, the results indicated that the sputum YKL-40 levels in patients with COPD were also significantly higher than those in healthy controls (SMD =0.70, 95% CI =0.10–1.30, P=0.022). CONCLUSION: The current study suggests that YKL-40 may be implicated in bronchial inflammation and remodeling in COPD and may be considered as a useful biomarker for COPD diagnosis and monitoring. Dove Medical Press 2018-01-30 /pmc/articles/PMC5796800/ /pubmed/29430175 http://dx.doi.org/10.2147/COPD.S152655 Text en © 2018 Tong 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 Tong, Xiang Wang, Dongguang Liu, Sitong Ma, Yao Li, Zhenzhen Tian, Panwen Fan, Hong The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title | The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title_full | The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title_fullStr | The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title_full_unstemmed | The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title_short | The YKL-40 protein is a potential biomarker for COPD: a meta-analysis and systematic review |
title_sort | ykl-40 protein is a potential biomarker for copd: a meta-analysis and systematic review |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796800/ https://www.ncbi.nlm.nih.gov/pubmed/29430175 http://dx.doi.org/10.2147/COPD.S152655 |
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