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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...

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Autores principales: Nakanishi, Yu, Horimasu, Yasushi, Yamaguchi, Kakuhiro, Sakamoto, Shinjiro, Masuda, Takeshi, Nakashima, Taku, Miyamoto, Shintaro, Iwamoto, Hiroshi, Ohshimo, Shinichiro, Fujitaka, Kazunori, Hamada, Hironobu, Hattori, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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.
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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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