Serum miR-502: A potential biomarker in the diagnosis of concussion in a pilot study of patients with normal structural brain imaging

D. Davies, K. Yakoub, Ugo Scarpa, Connor Bentley, M. Grey, D. Hammond, V. Sawlani, A. Belli, V. Di Pietro
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引用次数: 2

Abstract

Establishing a diagnosis of concussion within the context of competitive sport is frequently difficult due to the heterogeneity of presentation. Over the years, many endogenous proteins, including the recent Food and Drug Administration approved for mild-to-moderate traumatic brain injury, glial fibrillary acid protein and ubiquitin carboxy-terminal hydrolase, have been studied as potential biomarkers for the diagnosis of mild traumatic brain injury. Recently, a new class of potential biomarkers, the microRNAs, has shown promise as indicators of traumatic brain injury. In this pilot study, we have analysed the ability of pre-validated serum microRNAs (mi-425-5p and miR-502) to diagnose concussion, in cases without structural pathology. Their performance has been assessed alongside a set of identified protein biomarkers for traumatic brain injury in cohort of 41 concussed athletes. Athletes with a confirmed concussion underwent blood sampling after 48 h from concussion along with magnetic resonance imaging. Serum mi-425-5p and miR-502 were analysed by quantitative reverse transcription polymerase chain reaction, and digital immunoassay was used to determine serum concentrations of ubiquitin carboxy-terminal hydrolase, glial fibrillary acid protein, neurofilament light and Tau. Results were matched with 15 healthy volunteers. No structural/haemorrhagic pathology was identified. Protein biomarkers demonstrated variability among groups reflecting previous performance in the literature. Neurofilament light was the only marker to positively correlate with symptoms reported and SCAT5 scores. Despite the sub optimal timing of sampling beyond the optimal window for many of the protein biomarkers measured, miR-502 was significantly downregulated at all time points within a week form concussion ictus, showing a diagnostic sensitivity in cases beyond 48 h and without structural pathology.
血清miR-502:在正常脑结构成像患者的初步研究中诊断脑震荡的潜在生物标志物
由于表现的异质性,在竞技体育的背景下建立脑震荡的诊断通常是困难的。多年来,许多内源性蛋白,包括最近美国食品和药物管理局批准用于轻中度创伤性脑损伤的蛋白,胶质纤维酸蛋白和泛素羧基端水解酶,已经被研究作为诊断轻度创伤性脑损伤的潜在生物标志物。最近,一类新的潜在生物标志物,microRNAs,已经显示出作为创伤性脑损伤指标的希望。在这项初步研究中,我们分析了预先验证的血清microrna (mi-425-5p和miR-502)在没有结构病理的情况下诊断脑震荡的能力。在41名脑震荡运动员的队列中,他们的表现与一组确定的创伤性脑损伤蛋白质生物标志物一起进行了评估。确诊脑震荡的运动员在脑震荡48小时后接受了血液采样和磁共振成像。采用定量逆转录聚合酶链反应分析血清mi-425-5p和miR-502,采用数字免疫分析法测定血清泛素羧基端水解酶、胶质原纤维酸蛋白、神经丝光和Tau的浓度。结果与15名健康志愿者相匹配。未发现结构性/出血性病理。蛋白质生物标记物在不同的组中表现出可变性,反映了文献中先前的表现。神经丝光是唯一与症状报告和SCAT5评分呈正相关的标记物。尽管对于许多测量的蛋白质生物标志物来说,在最佳窗口之外的采样时间不是最佳的,但miR-502在脑震荡后一周内的所有时间点都显着下调,在超过48小时且没有结构病理的病例中显示出诊断敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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