Department of Human Pathology of Adulthood and Childhood 'G. Barresi', University of Messina, Messina, Italy.
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Mol Biol Rep. 2020 Apr;47(4):2941-2949. doi: 10.1007/s11033-020-05386-7. Epub 2020 Mar 26.
TBI is the main cause of death and disability in individuals aged 1-45 in Western countries. One of the main challenges of TBI at present is the lack of specific diagnostic biomarkers, especially for mild TBI (mTBI), which remains currently difficult to value in clinical practice. In this context MiRNAs may be important mediators of the profound molecular and cellular changes that occur after TBI in both the short and the long term. Recently, plasma miRNAs profiling in human TBI, have revealed dynamic temporal regulation of miRNA expression within the cortex. Aim of this study was to select a specific miRNAs panel for mTBI, by focusing the research on the prognostic meaning of miRNAs in the hours following the trauma, in order to be able to use this MIRNAs as potential biomarkers useful for monitoring the follow up of mild TBI. Serum levels of 17 miRNAs were measured by RT-quantitative polymerase chain reaction (qPCR) in 20 patients with mTBI at three different time-points (0 h, 24 h, 48 h) and in 10 controls. For 15 miRNAs we found a significant differences in the comparison among the three time points: for each of these miRNAs the values were greater at baseline and progressively reduced at 24 h and 48 h. These data allow us to consider the miRNAs included in panel as sensitive and specific biomarkers for mTBI, useful in monitoring the post-trauma period.
外伤性脑损伤(TBI)是西方国家 1-45 岁人群的主要死亡和致残原因。目前 TBI 的主要挑战之一是缺乏特异性诊断生物标志物,尤其是对于轻度 TBI(mTBI),目前在临床实践中仍难以评估。在这种情况下,miRNAs 可能是 TBI 后短时间和长时间内发生的深刻分子和细胞变化的重要介质。最近,对人类 TBI 中血浆 miRNAs 谱的研究揭示了 miRNA 表达在皮质内的动态时间调节。本研究的目的是通过聚焦于 miRNA 在创伤后数小时内的预后意义,选择用于 mTBI 的特定 miRNAs 面板,以便能够将这些 miRNAs 用作监测轻度 TBI 随访的潜在生物标志物。在 20 名 mTBI 患者和 10 名对照者的三个不同时间点(0 h、24 h、48 h),通过逆转录定量聚合酶链反应(qPCR)测量了 17 种 miRNAs 的血清水平。在这三个时间点的比较中,我们发现 15 种 miRNA 存在显著差异:对于这些 miRNA 中的每一种,其值在基线时较高,并在 24 h 和 48 h 时逐渐降低。这些数据使我们能够将纳入面板的 miRNAs 视为 mTBI 的敏感和特异性生物标志物,可用于监测创伤后时期。