Dynamic changes in peripheral blood-targeted miRNA expression profiles in patients with severe traumatic brain injury at high altitude

• Published in: Military medical research 2019-04, Vol.6 (1), p.12-12, Article 12
• Main Authors: Ma, Si-Qing, Xu, Xue-Xia, He, Zong-Zhao, Li, Xin-Hui, Luo, Jun-Ming
• Format: Article
• Language: English
• Subjects: Adult; Altitude; Brain Injuries, Traumatic - blood; Brain Injuries, Traumatic - genetics; DNA Damage; Female; Gene expression; Genomics; High altitude; Humans; Hypoxia; Intensive care; Male; MicroRNAs; MicroRNAs - blood; MicroRNAs - genetics; Middle Aged; miRNA expression profile; Physiology; Prospective Studies; Real-Time Polymerase Chain Reaction; Severe traumatic brain injury; Software; Trauma; Traumatic brain injury
• ISSN: 2054-9369; 2095-7467; 2054-9369
• DOI: 10.1186/s40779-019-0203-z

The aim of this work is to detect and compare the peripheral blood miRNA expression profiles in patients with severe traumatic brain injury (sTBI) 2, 12, 24, 48, and 72 h after injury at high altitude and to predict the target genes of differential expressed miRNAs. Twenty sTBI patients from high-altitude areas were randomly selected according to the inclusion and exclusion criteria and were divided into five groups: the 2-h group, 12-h group, 24-h group, 48-h group, and 72-h group. Peripheral blood miRNA expression profiles were detected using real-time quantitative PCR (qRT-PCR). The expression levels of miR-18a, miR-203, miR-146a, miR-149, miR-23b, and miR-let-7b in peripheral blood showed significant differences between the 2-h group and the 12-h group. The expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f in peripheral blood were up-regulated in the 24-h group. In the 48-h group, the expression levels of miR-181d, miR-29a, and miR-18b were upregulated. In the 72-h group, the expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f changed. The main target genes of the differentiation expressed miRNAs were genes that regulate inflammatory responses, apoptosis, and DNA damage/repair. miRNAs may be involved in the pathogenesis of sTBI by dynamically regulating the target genes that regulate inflammatory responses, apoptosis, and DNA damage/repair pathways.