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创伤性脑损伤中蛋白质生物标志物的最新研究进展,重点介绍成人和儿科的临床应用。

Update on protein biomarkers in traumatic brain injury with emphasis on clinical use in adults and pediatrics.

机构信息

Department of Neurosurgery, University of Pécs, Rét u. 2., 7623, Pécs, Hungary.

出版信息

Acta Neurochir (Wien). 2010 Jan;152(1):1-17. doi: 10.1007/s00701-009-0463-6. Epub 2009 Aug 4.

Abstract

PURPOSE

This review summarizes protein biomarkers in mild and severe traumatic brain injury in adults and children and presents a strategy for conducting rationally designed clinical studies on biomarkers in head trauma.

METHODS

We performed an electronic search of the National Library of Medicine's MEDLINE and Biomedical Library of University of Pennsylvania database in March 2008 using a search heading of traumatic head injury and protein biomarkers. The search was focused especially on protein degradation products (spectrin breakdown product, c-tau, amyloid-beta(1-42)) in the last 10 years, but recent data on "classical" markers (S-100B, neuron-specific enolase, etc.) were also examined.

RESULTS

We identified 85 articles focusing on clinical use of biomarkers; 58 articles were prospective cohort studies with injury and/or outcome assessment.

CONCLUSIONS

We conclude that only S-100B in severe traumatic brain injury has consistently demonstrated the ability to predict injury and outcome in adults. The number of studies with protein degradation products is insufficient especially in the pediatric care. Cohort studies with well-defined end points and further neuroproteomic search for biomarkers in mild injury should be triggered. After critically reviewing the study designs, we found that large homogenous patient populations, consistent injury, and outcome measures prospectively determined cutoff values, and a combined use of different predictors should be considered in future studies.

摘要

目的

本综述总结了成人和儿童轻度和重度创伤性脑损伤的蛋白质生物标志物,并提出了在头部创伤中进行合理设计的生物标志物临床研究的策略。

方法

我们于 2008 年 3 月使用国家医学图书馆 MEDLINE 和宾夕法尼亚大学生物医学图书馆的搜索标题“创伤性头部损伤和蛋白质生物标志物”,对国家医学图书馆的 MEDLINE 和宾夕法尼亚大学生物医学图书馆数据库进行了电子搜索。搜索特别集中在过去 10 年中蛋白质降解产物(血影蛋白分解产物、c-tau、淀粉样β(1-42)),但也检查了“经典”标志物(S-100B、神经元特异性烯醇化酶等)的最新数据。

结果

我们确定了 85 篇重点关注生物标志物临床应用的文章;58 篇是前瞻性队列研究,包括损伤和/或结局评估。

结论

我们的结论是,只有 S-100B 在严重创伤性脑损伤中一致显示出能够预测成人的损伤和结局的能力。蛋白质降解产物的研究数量不足,尤其是在儿科护理中。应该启动具有明确终点的队列研究,并进一步进行神经保护组学搜索以寻找轻度损伤的生物标志物。在对研究设计进行严格审查后,我们发现,在未来的研究中,应考虑大的同质患者群体、一致的损伤和结局测量、前瞻性确定的截断值以及不同预测因子的联合使用。

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