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IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a chronic, fibrosing interstitial pneumonia that presents with various clinical courses and progression ranging from rapid to slow. To identify novel biomarkers that can support the diagnosis and/or prognostic prediction of idiopathic pulmonary fibrosis, we performed...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177514/ https://www.ncbi.nlm.nih.gov/pubmed/34086758 http://dx.doi.org/10.1371/journal.pone.0252594 |
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author | Nakanishi, Yu Horimasu, Yasushi Yamaguchi, Kakuhiro Sakamoto, Shinjiro Masuda, Takeshi Nakashima, Taku Miyamoto, Shintaro Iwamoto, Hiroshi Ohshimo, Shinichiro Fujitaka, Kazunori Hamada, Hironobu Hattori, Noboru |
author_facet | Nakanishi, Yu Horimasu, Yasushi Yamaguchi, Kakuhiro Sakamoto, Shinjiro Masuda, Takeshi Nakashima, Taku Miyamoto, Shintaro Iwamoto, Hiroshi Ohshimo, Shinichiro Fujitaka, Kazunori Hamada, Hironobu Hattori, Noboru |
author_sort | Nakanishi, Yu |
collection | PubMed |
description | Idiopathic pulmonary fibrosis is a chronic, fibrosing interstitial pneumonia that presents with various clinical courses and progression ranging from rapid to slow. To identify novel biomarkers that can support the diagnosis and/or prognostic prediction of idiopathic pulmonary fibrosis, we performed gene expression analysis, and the mRNA of interleukin-18 binding protein was increasingly expressed in patients with idiopathic pulmonary fibrosis compared with healthy controls. Therefore, we hypothesized that the interleukin-18 binding protein can serve as a diagnostic and/or prognostic biomarker for idiopathic pulmonary fibrosis. We investigated the expression of interleukin-18 binding protein in lung tissue, bronchoalveolar lavage fluid, and serum. Additionally, the correlation between interleukin-18 binding protein expression levels and the extent of fibrosis was investigated using mouse models of lung fibrosis induced by subcutaneous bleomycin injections. Serum interleukin-18 binding protein levels were significantly higher in idiopathic pulmonary fibrosis patients (5.06 ng/mL, interquartile range [IQR]: 4.20–6.35) than in healthy volunteers (3.31 ng/mL, IQR: 2.84–3.99) (p < 0.001). Multivariate logistic regression models revealed that the correlation between serum interleukin-18 binding protein levels and idiopathic pulmonary fibrosis was statistically independent after adjustment for age, sex, and smoking status. Multivariate Cox proportional hazard models revealed that serum interleukin-18 binding protein levels were predictive of idiopathic pulmonary fibrosis disease prognosis independent of other covariate factors (hazard ratio: 1.655, 95% confidence interval: 1.224–2.237, p = 0.001). We also demonstrated a significant positive correlation between lung hydroxyproline expression levels and interleukin-18 binding protein levels in bronchoalveolar lavage fluid from bleomycin-treated mice (Spearman r = 0.509, p = 0.004). These results indicate the utility of interleukin-18 binding protein as a novel prognostic biomarker for idiopathic pulmonary fibrosis. |
format | Online Article Text |
id | pubmed-8177514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81775142021-06-07 IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis Nakanishi, Yu Horimasu, Yasushi Yamaguchi, Kakuhiro Sakamoto, Shinjiro Masuda, Takeshi Nakashima, Taku Miyamoto, Shintaro Iwamoto, Hiroshi Ohshimo, Shinichiro Fujitaka, Kazunori Hamada, Hironobu Hattori, Noboru PLoS One Research Article Idiopathic pulmonary fibrosis is a chronic, fibrosing interstitial pneumonia that presents with various clinical courses and progression ranging from rapid to slow. To identify novel biomarkers that can support the diagnosis and/or prognostic prediction of idiopathic pulmonary fibrosis, we performed gene expression analysis, and the mRNA of interleukin-18 binding protein was increasingly expressed in patients with idiopathic pulmonary fibrosis compared with healthy controls. Therefore, we hypothesized that the interleukin-18 binding protein can serve as a diagnostic and/or prognostic biomarker for idiopathic pulmonary fibrosis. We investigated the expression of interleukin-18 binding protein in lung tissue, bronchoalveolar lavage fluid, and serum. Additionally, the correlation between interleukin-18 binding protein expression levels and the extent of fibrosis was investigated using mouse models of lung fibrosis induced by subcutaneous bleomycin injections. Serum interleukin-18 binding protein levels were significantly higher in idiopathic pulmonary fibrosis patients (5.06 ng/mL, interquartile range [IQR]: 4.20–6.35) than in healthy volunteers (3.31 ng/mL, IQR: 2.84–3.99) (p < 0.001). Multivariate logistic regression models revealed that the correlation between serum interleukin-18 binding protein levels and idiopathic pulmonary fibrosis was statistically independent after adjustment for age, sex, and smoking status. Multivariate Cox proportional hazard models revealed that serum interleukin-18 binding protein levels were predictive of idiopathic pulmonary fibrosis disease prognosis independent of other covariate factors (hazard ratio: 1.655, 95% confidence interval: 1.224–2.237, p = 0.001). We also demonstrated a significant positive correlation between lung hydroxyproline expression levels and interleukin-18 binding protein levels in bronchoalveolar lavage fluid from bleomycin-treated mice (Spearman r = 0.509, p = 0.004). These results indicate the utility of interleukin-18 binding protein as a novel prognostic biomarker for idiopathic pulmonary fibrosis. Public Library of Science 2021-06-04 /pmc/articles/PMC8177514/ /pubmed/34086758 http://dx.doi.org/10.1371/journal.pone.0252594 Text en © 2021 Nakanishi et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Nakanishi, Yu Horimasu, Yasushi Yamaguchi, Kakuhiro Sakamoto, Shinjiro Masuda, Takeshi Nakashima, Taku Miyamoto, Shintaro Iwamoto, Hiroshi Ohshimo, Shinichiro Fujitaka, Kazunori Hamada, Hironobu Hattori, Noboru IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title | IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title_full | IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title_fullStr | IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title_full_unstemmed | IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title_short | IL-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
title_sort | il-18 binding protein can be a prognostic biomarker for idiopathic pulmonary fibrosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177514/ https://www.ncbi.nlm.nih.gov/pubmed/34086758 http://dx.doi.org/10.1371/journal.pone.0252594 |
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