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

Author:

Furukawa Hiroshi123ORCID,Oka Shomi123,Shimada Kota45,Hashimoto Atsushi4,Komiya Akiko16,Matsui Toshihiro14,Fukui Naoshi1,Tohma Shigeto13

Affiliation:

1. Clinical Research Center for Allergy and Rheumatology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

2. Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

3. Department of Rheumatology, National Hospital Organization Tokyo National Hospital, Kiyose, Japan

4. Department of Rheumatology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

5. Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu, Japan

6. Department of Clinical Laboratory, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

Abstract

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.

Funder

japan society for the promotion of science

Ministry of Health, Labour, and Welfare of Japan

japan agency for medical research and development

Daiwa Securities Health

japan research foundation for clinical pharmacology

The Nakatomi Foundation

takeda science foundation

mitsui sumitomo insurance welfare foundation

Abbott Japan Co., Ltd

Astellas Pharma Inc

Chugai Pharmaceutical Co., Ltd.,

Eisai Co., Ltd.,

Mitsuibishi Tanabe Pharma Corporation

Merck Sharp and Dohme Inc

Pfizer Japan Inc.

Takeda Pharmaceutical Company Limited

Teijin Pharma Limited.

Publisher

SAGE Publications

Subject

Biochemistry, medical,Pharmacology,Molecular Medicine

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