miRNA Expression Profiles and Potential as Biomarkers in Nontuberculous Mycobacterial Pulmonary Disease

• Published in: Scientific reports 2020-02, Vol.10 (1), p.3178, Article 3178
• Main Authors: Han, Sun Ae, Jhun, Byung Woo, Kim, Su-Young, Moon, Seong Mi, Yang, Bumhee, Kwon, O. Jung, Daley, Charles L., Shin, Sung Jae, Koh, Won-Jung
• Format: Article
• Language: English
• Subjects: 13/31; 38/91; 631/337/384/331; 692/699/255/1318; Area Under Curve; Bioinformatics; Biomarkers; Biomarkers - metabolism; Case-Control Studies; Cluster Analysis; Female; Gene Expression Profiling; Gene Expression Regulation; Gene Ontology; Gene Regulatory Networks; Humanities and Social Sciences; Humans; Immune response; Lung diseases; Lung Diseases - blood; Lung Diseases - complications; Lung Diseases - genetics; Male; MicroRNAs - blood; MicroRNAs - genetics; MicroRNAs - metabolism; Middle Aged; miRNA; multidisciplinary; Mycobacterium Infections, Nontuberculous - blood; Mycobacterium Infections, Nontuberculous - complications; Mycobacterium Infections, Nontuberculous - genetics; Reproducibility of Results; ROC Curve; Science; Science (multidisciplinary); Sensitivity and Specificity
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-60132-0

Pulmonary disease (PD) due to nontuberculous mycobacteria (NTM) is increasing globally, but specific biomarkers for NTM-PD have not been established. As circulating miRNAs are promising biomarkers for various diseases, we investigated whether miRNAs have potential as NTM-PD biomarkers. Sera from 12 NTM-PD patients due to Mycobacterium avium , M. intracellulare , M. abscessus , or M. massiliense and three healthy controls were initially evaluated via small RNA sequencing. Multiple miRNAs showed significant differences in expression in patients compared to in healthy controls, with some expression differences unique to PD caused by a specific mycobacterial species. Notably, 14 miRNAs exhibited significant expression differences in PD associated with all four mycobacteria. Validation by quantitative reverse-transcription-PCR in an additional 40 patients with NTM-PD and 40 healthy controls confirmed that four differentially expressed miRNAs (hsa-miR-484, hsa-miR-584-5p, hsa-miR-625-3p, and hsa-miR-4732-5p) showed significantly higher serum expressions in NTM-PD patients than in controls. Receiver operating characteristic curve analysis of these four miRNAs supported the discriminative potential for NTM-PD and their combination provided an improved diagnostic value for NTM-PD. Furthermore, bioinformatics analysis revealed their 125 target genes, which were mostly associated with immune responses. Collectively, this study identified four miRNAs as potential biomarkers for NTM-PD and provided insight into NTM-PD pathophysiology.