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Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease

OBJECTIVE: Acute-onset diffuse interstitial lung disease (AoDILD) includes acute exacerbation of interstitial lung disease (ILD), drug-induced ILD, and Pneumocystis pneumonia, and frequently occurs in patients with rheumatoid arthritis (RA). Since AoDILD causes a poor prognosis in RA, biomarkers for...

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Autores principales: Furukawa, Hiroshi, Oka, Shomi, Shimada, Kota, Hashimoto, Atsushi, Komiya, Akiko, Matsui, Toshihiro, Fukui, Naoshi, Tohma, Shigeto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709435/
https://www.ncbi.nlm.nih.gov/pubmed/31488947
http://dx.doi.org/10.1177/1177271919870472
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author Furukawa, Hiroshi
Oka, Shomi
Shimada, Kota
Hashimoto, Atsushi
Komiya, Akiko
Matsui, Toshihiro
Fukui, Naoshi
Tohma, Shigeto
author_facet Furukawa, Hiroshi
Oka, Shomi
Shimada, Kota
Hashimoto, Atsushi
Komiya, Akiko
Matsui, Toshihiro
Fukui, Naoshi
Tohma, Shigeto
author_sort Furukawa, Hiroshi
collection PubMed
description OBJECTIVE: Acute-onset diffuse interstitial lung disease (AoDILD) includes acute exacerbation of interstitial lung disease (ILD), drug-induced ILD, and Pneumocystis pneumonia, and frequently occurs in patients with rheumatoid arthritis (RA). Since AoDILD causes a poor prognosis in RA, biomarkers for AoDILD were eagerly desired. Metabolomic analyses were extensively performed in cancer patients and successfully generated better diagnostic biomarkers. In the present study, serum metabolomic profiles of AoDILD in RA were investigated to generate better potential metabolomic biomarkers. METHODS: Serum samples of 10 RA patients with AoDILD were collected on admission and in a stable state, more than 3 months before the admission. Serum metabolomic analyses were conducted on the samples from these RA patients with AoDILD. RESULTS: Apparently distinct serum metabolomic profiles in AoDILD were not observed in univariate or hierarchical cluster analyses. Partial least squares-discriminant analysis (PLS-DA) was performed to select candidate metabolites based on variable importance in projection (VIP) scores. The PLS-DA model generated from the four metabolites with VIP scores more than 2.25 (mannosamine, alliin, kynurenine, and 2-hydroxybutyric acid) could successfully discriminate AoDILD from the stable condition (area under the curve: 0.962, 95% confidence interval: 0.778–1.000). CONCLUSION: It was demonstrated that metabolomic profiling was useful to generate better biomarkers in AoDILD.
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spelling pubmed-67094352019-09-05 Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease Furukawa, Hiroshi Oka, Shomi Shimada, Kota Hashimoto, Atsushi Komiya, Akiko Matsui, Toshihiro Fukui, Naoshi Tohma, Shigeto Biomark Insights Original Research OBJECTIVE: Acute-onset diffuse interstitial lung disease (AoDILD) includes acute exacerbation of interstitial lung disease (ILD), drug-induced ILD, and Pneumocystis pneumonia, and frequently occurs in patients with rheumatoid arthritis (RA). Since AoDILD causes a poor prognosis in RA, biomarkers for AoDILD were eagerly desired. Metabolomic analyses were extensively performed in cancer patients and successfully generated better diagnostic biomarkers. In the present study, serum metabolomic profiles of AoDILD in RA were investigated to generate better potential metabolomic biomarkers. METHODS: Serum samples of 10 RA patients with AoDILD were collected on admission and in a stable state, more than 3 months before the admission. Serum metabolomic analyses were conducted on the samples from these RA patients with AoDILD. RESULTS: Apparently distinct serum metabolomic profiles in AoDILD were not observed in univariate or hierarchical cluster analyses. Partial least squares-discriminant analysis (PLS-DA) was performed to select candidate metabolites based on variable importance in projection (VIP) scores. The PLS-DA model generated from the four metabolites with VIP scores more than 2.25 (mannosamine, alliin, kynurenine, and 2-hydroxybutyric acid) could successfully discriminate AoDILD from the stable condition (area under the curve: 0.962, 95% confidence interval: 0.778–1.000). CONCLUSION: It was demonstrated that metabolomic profiling was useful to generate better biomarkers in AoDILD. SAGE Publications 2019-08-22 /pmc/articles/PMC6709435/ /pubmed/31488947 http://dx.doi.org/10.1177/1177271919870472 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Furukawa, Hiroshi
Oka, Shomi
Shimada, Kota
Hashimoto, Atsushi
Komiya, Akiko
Matsui, Toshihiro
Fukui, Naoshi
Tohma, Shigeto
Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title_full Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title_fullStr Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title_full_unstemmed Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title_short Serum Metabolomic Profiles of Rheumatoid Arthritis Patients With Acute-Onset Diffuse Interstitial Lung Disease
title_sort serum metabolomic profiles of rheumatoid arthritis patients with acute-onset diffuse interstitial lung disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709435/
https://www.ncbi.nlm.nih.gov/pubmed/31488947
http://dx.doi.org/10.1177/1177271919870472
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