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创伤性脑损伤生物标志物的进展

Advances in Traumatic Brain Injury Biomarkers.

作者信息

Nishimura Kengo, Cordeiro Joacir G, Ahmed Aminul I, Yokobori Shoji, Gajavelli Shyam

机构信息

Neurological Surgery, University of Miami, Miami, USA.

Wolfson Centre for Age-Related Diseases, King's College London, London, GBR.

出版信息

Cureus. 2022 Apr 4;14(4):e23804. doi: 10.7759/cureus.23804. eCollection 2022 Apr.

Abstract

Traumatic brain injury (TBI) is increasingly a major cause of disability across the globe. The current methods of diagnosis are inadequate at classifying patients and prognosis. TBI is a diagnostic and therapeutic challenge. There is no Food and Drug Administration (FDA)-approved treatment for TBI yet. It took about 16 years of preclinical research to develop accurate and objective diagnostic measures for TBI. Two brain-specific protein biomarkers, namely, ubiquitin C-terminal hydrolase-L1 and glial fibrillary acidic protein, have been extensively characterized. Recently, the two biomarkers were approved by the FDA as the first blood-based biomarker, Brain Trauma Indicator™ (BTI™), via the Breakthrough Devices Program. This scoping review presents (i) TBI diagnosis challenges, (ii) the process behind the FDA approval of biomarkers, and (iii) known unknowns in TBI biomarker biology. The current lag in TBI incidence and hospitalization can be reduced if digital biomarkers such as hard fall detection are standardized and used as a mechanism to alert paramedics to an unresponsive trauma patient.

摘要

创伤性脑损伤(TBI)日益成为全球致残的主要原因。目前的诊断方法在对患者进行分类和预后评估方面存在不足。TBI是一个诊断和治疗方面的挑战。目前尚无美国食品药品监督管理局(FDA)批准的针对TBI的治疗方法。为开发准确、客观的TBI诊断方法进行了约16年的临床前研究。两种脑特异性蛋白质生物标志物,即泛素C末端水解酶-L1和胶质纤维酸性蛋白,已得到广泛表征。最近,这两种生物标志物通过“突破性设备计划”被FDA批准为首个基于血液的生物标志物——脑创伤指标(BTI™)。本综述介绍了(i)TBI诊断面临的挑战,(ii)FDA批准生物标志物背后的过程,以及(iii)TBI生物标志物生物学中已知的未知因素。如果诸如硬跌倒检测等数字生物标志物能够标准化,并用作提醒护理人员注意无反应创伤患者的机制,那么目前TBI发病率和住院率方面的滞后情况可能会得到缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e66/8978594/885f0ea8fbbb/cureus-0014-00000023804-i01.jpg

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