MicroRNA Signatures Associated with Bronchopulmonary Dysplasia Severity in Tracheal Aspirates of Preterm Infants

• Published in: Biomedicines Vol. 9; no. 3; p. 257
• Main Authors: Siddaiah, Roopa, Oji-Mmuo, Christiana N, Montes, Deborah T, Fuentes, Nathalie, Spear, Debra, Donnelly, Ann, Silveyra, Patricia
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 05.03.2021; MDPI
• Subjects: Biomarkers; Birth weight; bronchopulmonary dysplasia; Classification; Congenital diseases; Dysplasia; Fetuses; Gene expression; Infants; Inflammation; Intensive care; Lung diseases; MicroRNAs; miRNA; Neonates; Newborn babies; Ostomy; Pathogenesis; Premature birth; prematurity; tracheal aspirates; Ventilators; United States > US; miRNA; prematurity; tracheal aspirates; bronchopulmonary dysplasia; biomarkers
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines9030257

Bronchopulmonary dysplasia (BPD) is a form of chronic lung disease that develops in neonates as a consequence of preterm birth, arrested fetal lung development, and inflammation. The incidence of BPD remains on the rise as a result of increasing survival of extremely preterm infants. Severe BPD contributes to significant health care costs and is associated with prolonged hospitalizations, respiratory infections, and neurodevelopmental deficits. In this study, we aimed to detect novel biomarkers of BPD severity. We collected tracheal aspirates (TAs) from preterm babies with mild/moderate ( = 8) and severe ( = 17) BPD, and we profiled the expression of 1048 miRNAs using a PCR array. Associations with biological pathways were determined with the Ingenuity Pathway Analysis (IPA) software. We found 31 miRNAs differentially expressed between the two disease groups (2-fold change, false discovery rate (FDR) < 0.05). Of these, 4 miRNAs displayed significantly higher expression levels, and 27 miRNAs had significantly lower expression levels in the severe BPD group when compared to the mild/moderate BPD group. IPA identified cell signaling and inflammation pathways associated with miRNA signatures. We conclude that TAs of extremely premature infants contain miRNA signatures associated with severe BPD. These may serve as potential biomarkers of disease severity in infants with BPD.