An overview of mild traumatic brain injuries and emerging therapeutic targets

被引:6
|
作者
Bielanin, John P. [1 ,2 ,3 ]
Metwally, Shamseldin A. H. [2 ,3 ]
Paruchuri, Satya S. [2 ,3 ]
Sun, Dandan [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Pittsburgh Inst Neurodegenerat Disorders, Pittsburgh, PA 15213 USA
[4] Vet Affairs Pittsburgh Hlth Care Syst, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Dept Neurol, 7016 Biomed Sci Tower 3 3501 Fifth Ave, Pittsburgh, PA 15260 USA
关键词
Axonal damage; Demyelination; Inflammation; mTBI; Oxidative stress;
D O I
10.1016/j.neuint.2023.105655
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The majority of traumatic brain injuries (TBIs), approximately 90%, are classified as mild (mTBIs). Globally, an estimated 4 million injuries occur each year from concussions or mTBIs, highlighting their significance as a public health crisis. TBIs can lead to substantial long-term health consequences, including an increased risk of developing Alzheimer's Disease, Parkinson's Disease (PD), chronic traumatic encephalopathy (CTE), and nearly doubling one's risk of suicide. However, the current management of mTBIs in clinical practice and the available treatment options are limited. There exists an unmet need for effective therapy. This review addresses various aspects of mTBIs based on the most up-to-date literature review, with the goal of stimulating translational research to identify new therapeutic targets and improve our understanding of pathogenic mechanisms. First, we provide a summary of mTBI symptomatology and current diagnostic parameters such as the Glasgow Coma Scale (GCS) for classifying mTBIs or concussions, as well as the utility of alternative diagnostic parameters, including imaging techniques like MRI with diffusion tensor imaging (DTI) and serum biomarkers such as S100B, NSE, GFAP, UCH-L1, NFL, and t-tau. Our review highlights several pre-clinical concussion models employed in the study of mTBIs and the underlying cellular mechanisms involved in mTBI-related pathogenesis, including axonal damage, demyelination, inflammation, and oxidative stress. Finally, we examine a selection of new therapeutic targets currently under investigation in pre-clinical models. These targets may hold promise for clinical translation and address the pressing need for more effective treatments for mTBIs.
引用
收藏
页数:11
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