a Program for Neurotrauma, Neuroproteomics & Biomarkers Research, Departments of Emergency Medicine, Psychiatry, Neuroscience and Chemistry , University of Florida , Gainesville , Florida , USA.
b Department Of Pediatrics, Daping Hospital, Chongqing , Third Military Medical University , Chongqing , China.
Expert Rev Mol Diagn. 2018 Feb;18(2):165-180. doi: 10.1080/14737159.2018.1428089. Epub 2018 Jan 23.
Traumatic brain injury (TBI) is a major worldwide neurological disorder of epidemic proportions. To date, there are still no FDA-approved therapies to treat any forms of TBI. Encouragingly, there are emerging data showing that biofluid-based TBI biomarker tests have the potential to diagnose the presence of TBI of different severities including concussion, and to predict outcome. Areas covered: The authors provide an update on the current knowledge of TBI biomarkers, including protein biomarkers for neuronal cell body injury (UCH-L1, NSE), astroglial injury (GFAP, S100B), neuronal cell death (αII-spectrin breakdown products), axonal injury (NF proteins), white matter injury (MBP), post-injury neurodegeneration (total Tau and phospho-Tau), post-injury autoimmune response (brain antigen-targeting autoantibodies), and other emerging non-protein biomarkers. The authors discuss biomarker evidence in TBI diagnosis, outcome prognosis and possible identification of post-TBI neurodegernative diseases (e.g. chronic traumatic encephalopathy and Alzheimer's disease), and as theranostic tools in pre-clinical and clinical settings. Expert commentary: A spectrum of biomarkers is now at or near the stage of formal clinical validation of their diagnostic and prognostic utilities in the management of TBI of varied severities including concussions. TBI biomarkers could serve as a theranostic tool in facilitating drug development and treatment monitoring.
创伤性脑损伤 (TBI) 是一种具有流行规模的全球性重大神经疾病。迄今为止,仍然没有获得 FDA 批准的疗法可以治疗任何形式的 TBI。令人鼓舞的是,有新出现的数据表明,基于生物流体的 TBI 生物标志物测试有可能诊断出不同严重程度的 TBI 的存在,包括脑震荡,并预测结果。涵盖领域:作者提供了 TBI 生物标志物当前知识的更新,包括神经元细胞体损伤的蛋白质生物标志物(UCH-L1、NSE)、星形胶质细胞损伤(GFAP、S100B)、神经元细胞死亡(αII- spectrin 断裂产物)、轴突损伤(NF 蛋白)、白质损伤(MBP)、损伤后神经退行性变(总 Tau 和磷酸化 Tau)、损伤后自身免疫反应(针对脑抗原的靶向自身抗体)以及其他新兴的非蛋白质生物标志物。作者讨论了 TBI 诊断、预后和可能识别损伤后神经退行性疾病(例如慢性创伤性脑病和阿尔茨海默病)的生物标志物证据,以及在临床前和临床环境中作为治疗诊断工具的用途。专家评论:现在有一系列生物标志物已经或接近正式临床验证阶段,以验证它们在管理不同严重程度的 TBI(包括脑震荡)中的诊断和预后效用。TBI 生物标志物可以作为一种治疗诊断工具,促进药物开发和治疗监测。