Azar Safa, Hasan Anwarul, Younes Richard, Najdi Farah, Baki Lama, Ghazale Hussein, Kobeissy Firas H, Zibara Kazem, Mondello Stefania
Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Department of Mechanical and Industrial Engineering, Qatar University, Doha, Qatar.
Methods Mol Biol. 2017;1598:45-63. doi: 10.1007/978-1-4939-6952-4_3.
Traumatic brain injury (TBI) is an injury to the brain caused by an external mechanical force, affecting millions of people worldwide. The disease course and prognosis are often unpredictable, and it can be challenging to determine an early diagnosis in case of mild injury as well as to accurately phenotype the injury. There is currently no cure for TBI-drugs having failed repeatedly in clinical trials-but an intense effort has been put to identify effective neuroprotective treatment. The detection of novel biomarkers, to understand more of the disease mechanism, facilitates early diagnosis, predicts disease progression, and develops molecularly targeted therapies that would be of high clinical interest. Over the last decade, there has been an increasing effort and initiative toward finding TBI-specific biomarker candidates. One promising strategy has been to use state-of-the-art neuroproteomics approaches to assess clinical biofluids and compare the cerebrospinal fluid (CSF) and blood proteome between TBI and control patients or between different subgroups of TBI. In this chapter, we summarize and discuss the status of biofluid proteomics in TBI, with a particular focus on the latest findings.
创伤性脑损伤(TBI)是由外部机械力导致的脑损伤,影响着全球数百万人。其病程和预后往往不可预测,对于轻度损伤病例,早期诊断具有挑战性,准确描述损伤类型也很困难。目前尚无治疗TBI的方法——药物在临床试验中多次失败——但人们一直在努力寻找有效的神经保护治疗方法。检测新型生物标志物以更好地了解疾病机制,有助于早期诊断、预测疾病进展,并开发具有高度临床意义的分子靶向疗法。在过去十年中,人们越来越努力并积极寻找TBI特异性生物标志物候选物。一种有前景的策略是使用最先进的神经蛋白质组学方法来评估临床生物流体,并比较TBI患者与对照患者之间或TBI不同亚组之间的脑脊液(CSF)和血液蛋白质组。在本章中,我们总结并讨论了TBI中生物流体蛋白质组学的现状,特别关注最新研究结果。