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血清SNTF,一种轴突损伤的替代标志物,对急诊科治疗的轻度创伤性脑损伤患者持续脑功能障碍具有预后价值。

Serum SNTF, a Surrogate Marker of Axonal Injury, Is Prognostic for Lasting Brain Dysfunction in Mild TBI Treated in the Emergency Department.

作者信息

Siman Robert, Cui Hongmei, Wewerka Sandi S, Hamel Lydia, Smith Douglas H, Zwank Michael D

机构信息

Department of Neurosurgery, Center for Brain Injury and Repair, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

Department of Emergency Medicine, Regions Hospital, St. Paul, MN, United States.

出版信息

Front Neurol. 2020 Apr 8;11:249. doi: 10.3389/fneur.2020.00249. eCollection 2020.

Abstract

Mild traumatic brain injury (mTBI) causes persisting post-concussion syndrome for many patients without abnormalities on conventional neuroimaging. Currently, there is no method for identifying at-risk cases at an early stage for directing concussion management and treatment. SNTF is a calpain-derived N-terminal proteolytic fragment of spectrin (α-spectrin1-1176) generated in damaged axons following mTBI. Preliminary human studies suggest that elevated blood SNTF on the day of mTBI correlates with white matter disruption and lasting brain dysfunction. Here, we further evaluated serum SNTF as a prognostic marker for persistent brain dysfunction in uncomplicated mTBI patients treated in a Level I trauma center emergency department. Compared with healthy controls ( = 40), serum SNTF increased by 92% within 24 h of mTBI ( = 95; < 0.0001), and as a diagnostic marker exhibited 100% specificity and 37% sensitivity (AUC = 0.87). To determine whether the subset of mTBI cases positive for SNTF preferentially developed lasting brain dysfunction, serum levels on the day of mTBI were compared with multiple measures of brain performance at 90 days post-injury. Elevated serum SNTF correlated significantly with persistent impairments in cognition and sensory-motor integration, and predicted worse performance in each test on a case by case basis (AUC = 0.68 and 0.76, respectively). SNTF also predicted poorer recovery of cognitive stress function from 30 to 90 days (AUC = 0.79-0.90). These results suggest that serum SNTF, a surrogate marker for axonal injury after mTBI, may have potential for the rapid prognosis of lasting post-concussion syndrome and impaired functional recovery following CT-negative mTBI. They provide further evidence linking axonal injury to persisting brain dysfunction after uncomplicated mTBI. A SNTF blood test, either alone or combined with other markers of axonal injury, may have important utilities for research, prognosis, management and treatment of concussion.

摘要

轻度创伤性脑损伤(mTBI)会使许多患者出现持续的脑震荡后综合征,而传统神经影像学检查并无异常。目前,尚无方法能在早期识别出有风险的病例,以指导脑震荡的管理和治疗。SNTF是血影蛋白的一种源自钙蛋白酶的N端蛋白水解片段(α-血影蛋白1-1176),在mTBI后受损轴突中产生。初步人体研究表明,mTBI当天血液中SNTF升高与白质破坏及持久的脑功能障碍相关。在此,我们进一步评估血清SNTF作为在一级创伤中心急诊科接受治疗的单纯性mTBI患者持续性脑功能障碍的预后标志物。与健康对照组(n = 40)相比,mTBI后24小时内血清SNTF升高了92%(n = 95;P < 0.0001),作为诊断标志物,其特异性为100%,敏感性为37%(AUC = 0.87)。为确定SNTF呈阳性的mTBI病例亚组是否更易出现持久的脑功能障碍,将mTBI当天的血清水平与伤后90天的多项脑功能指标进行比较。血清SNTF升高与认知和感觉运动整合的持续受损显著相关,并在逐个病例基础上预测每次测试中更差的表现(AUC分别为0.68和0.76)。SNTF还预测了30至90天认知应激功能的较差恢复(AUC = 0.79 - 0.90)。这些结果表明,血清SNTF作为mTBI后轴突损伤的替代标志物,可能对脑震荡后综合征持续存在及CT阴性mTBI后功能恢复受损具有快速预后的潜力。它们为单纯性mTBI后轴突损伤与持续性脑功能障碍之间的联系提供了进一步证据。单独或与其他轴突损伤标志物联合的SNTF血液检测,可能对脑震荡的研究、预后、管理和治疗具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a16/7156622/ba57914532c9/fneur-11-00249-g0001.jpg

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