Metabolomic Characteristics of Nontuberculous Mycobacterial Pulmonary Disease

Author:

Kim Jungeun12,Chae Woori13,Kim Joong-Yub4,Yim Jae-Joon4,Cho Joo-Youn123,Kwak Nakwon4ORCID

Affiliation:

1. Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital , Seoul 03080 , Republic of Korea

2. Department of Biomedical Sciences, Seoul National University College of Medicine , Seoul 03080 , Republic of Korea

3. Kidney Research Institute, Seoul National University Medical Research Center , Seoul 03080 , Republic of Korea

4. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital , Seoul 03080 , Republic of Korea

Abstract

Abstract Background The therapeutic challenges posed by nontuberculous mycobacterial pulmonary disease (NTM-PD) contribute to an unmet medical need. In this study, we aimed to investigate NTM-PD-specific metabolic pathways using serum metabolomics to understand disease pathogenesis. Methods Mass spectrometry-based untargeted metabolomic profiling of serum from patients with NTM-PD (n = 50), patients with bronchiectasis (n = 50), and healthy controls (n = 60) was performed. Selected metabolites were validated by an independent cohort and subjected to pathway analysis and classification modeling. Results Leucine, tyrosine, inosine, proline, 5-oxoproline, and hypoxanthine levels increased in the NTM-PD group compared with the healthy control group. Furthermore, levels of antioxidant metabolites (ferulic acid, α-lipoic acid, biotin, and 2,8-phenazinediamine) decreased in patients with NTM-PD. These changes were associated with arginine- and proline-related metabolism, leading to generation of reactive oxygen species. Interestingly, the observed metabolic changes in the NTM-PD group overlapped with those in the bronchiectasis group. Conclusion In NTM-PD, 11 metabolites linked to increased oxidative stress were significantly altered from those in healthy controls. Our findings enhance a comprehensive understanding of NTM-PD pathogenesis and provide insights for novel treatment approaches.

Publisher

Oxford University Press (OUP)

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