Atif Hamna, Hicks Steven D
Department of Pediatrics, Penn State College of Medicine, Hershey, PA, USA.
J Exp Neurosci. 2019 Mar 8;13:1179069519832286. doi: 10.1177/1179069519832286. eCollection 2019.
There is growing public concern surrounding traumatic brain injury (TBI). TBI can cause significant morbidity, and the long-term sequelae are poorly understood. TBI diagnosis and management rely on patient-reported symptoms and subjective clinical assessment. There are no biologic tools to detect mild TBI or to track brain recovery. Emerging evidence suggests that microRNAs (miRNAs) may provide information about the injured brain. These tiny epigenetic molecules are expressed throughout the body. However, they are particularly important in neurons, can cross the blood-brain barrier, and are securely transported from cell to cell, where they regulate gene expression. miRNA levels may identify patients with TBI and predict symptom duration. This review synthesizes miRNA findings from 14 human studies. We distill more than 291 miRNAs to 17 biomarker candidates that overlap across multiple studies and multiple biofluids. The goal of this review is to establish a collective understanding of miRNA biology in TBI and identify clinical priorities for future investigations of this promising biomarker.
公众对创伤性脑损伤(TBI)的关注日益增加。TBI可导致严重的发病率,而其长期后遗症却知之甚少。TBI的诊断和管理依赖于患者报告的症状和主观临床评估。目前尚无检测轻度TBI或跟踪脑恢复情况的生物学工具。新出现的证据表明,微小RNA(miRNA)可能提供有关受伤大脑的信息。这些微小的表观遗传分子在全身表达。然而,它们在神经元中尤为重要,能够穿过血脑屏障,并在细胞间安全运输,在那里它们调节基因表达。miRNA水平可能有助于识别TBI患者并预测症状持续时间。本综述综合了14项人体研究中的miRNA研究结果。我们将291多种miRNA提炼为17种生物标志物候选物,这些候选物在多项研究和多种生物流体中存在重叠。本综述的目的是建立对TBI中miRNA生物学的共同理解,并确定对这一有前景的生物标志物进行未来研究的临床重点。