Biofluid Biomarkers in Traumatic Brain Injury: A Systematic Scoping Review

医学 格拉斯哥昏迷指数 创伤性脑损伤 格拉斯哥结局量表 人口 重症监护医学 生物标志物 病理 内科学 外科 精神科 生物化学 化学 环境卫生
作者
Maryam Edalatfar,Seyed Mohammad Piri,Mohammad-Mehdi Mehrabinejad,Monireh‐Sadat Mousavi,Sogol Meknatkhah,Mohammad Reza Fattahi,Zeinab Kavyani,Abdolkarim Haji Ghadery,Meysam Kaveh,Armin Aryannejad,Mohammad Ghafouri,Elham Jamshidi,Mohamad Mehdi Rezwanifar,Mohsen Sadeghi-Naini,Ausaf Bari,Mahdi Sharif-Alhoseini
出处
期刊:Neurocritical Care [Springer Science+Business Media]
卷期号:35 (2): 559-572 被引量:34
标识
DOI:10.1007/s12028-020-01173-1
摘要

Emerging evidence suggests that biofluid-based biomarkers have diagnostic and prognostic potential in traumatic brain injuries (TBI). However, owing to the lack of a conceptual framework or comprehensive review, it is difficult to visualize the breadth of materials that might be available. We conducted a systematic scoping review to map and categorize the evidence regarding biofluid-based biochemical markers of TBI. A comprehensive search was undertaken in January 2019. Of 25,354 records identified through the literature search, 1036 original human studies were included. Five hundred forty biofluid biomarkers were extracted from included studies and classified into 19 distinct categories. Three categories of biomarkers including cytokines, coagulation tests, and nerve tissue proteins were investigated more than others and assessed in almost half of the studies (560, 515, and 502 from 1036 studies, respectively). S100 beta as the most common biomarker for TBI was tested in 21.2% of studies (220 articles). Cortisol was the only biomarker measured in blood, cerebrospinal fluid, urine, and saliva. The most common sampling time was at admission and within 24 h of injury. The included studies focused mainly on biomarkers from blood and central nervous system sources, the adult population, and severe and blunt injuries. The most common outcome measures used in studies were changes in biomarker concentration level, Glasgow coma scale, Glasgow outcome scale, brain computed tomography scan, and mortality rate. Biofluid biomarkers could be clinically helpful in the diagnosis and prognosis of TBI. However, there was no single definitive biomarker with accurate characteristics. The present categorization would be a road map to investigate the biomarkers of the brain injury cascade separately and detect the most representative biomarker of each category. Also, this comprehensive categorization could provide a guiding framework to design combined panels of multiple biomarkers.
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