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Innovative Insights into Traumatic Brain Injuries: Biomarkers and New Pharmacological Targets

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Feb 24
PMID 38397046
Authors
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Abstract

A traumatic brain injury (TBI) is a major health issue affecting many people across the world, causing significant morbidity and mortality. TBIs often have long-lasting effects, disrupting daily life and functionality. They cause two types of damage to the brain: primary and secondary. Secondary damage is particularly critical as it involves complex processes unfolding after the initial injury. These processes can lead to cell damage and death in the brain. Understanding how these processes damage the brain is crucial for finding new treatments. This review examines a wide range of literature from 2021 to 2023, focusing on biomarkers and molecular mechanisms in TBIs to pinpoint therapeutic advancements. Baseline levels of biomarkers, including neurofilament light chain (NF-L), ubiquitin carboxy-terminal hydrolase-L1 (UCH-L1), Tau, and glial fibrillary acidic protein (GFAP) in TBI, have demonstrated prognostic value for cognitive outcomes, laying the groundwork for personalized treatment strategies. In terms of pharmacological progress, the most promising approaches currently target neuroinflammation, oxidative stress, and apoptotic mechanisms. Agents that can modulate these pathways offer the potential to reduce a TBI's impact and aid in neurological rehabilitation. Future research is poised to refine these therapeutic approaches, potentially revolutionizing TBI treatment.

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References
1.
Hier D, Obafemi-Ajayi T, Thimgan M, Olbricht G, Azizi S, Allen B . Blood biomarkers for mild traumatic brain injury: a selective review of unresolved issues. Biomark Res. 2021; 9(1):70. PMC: 8447604. DOI: 10.1186/s40364-021-00325-5. View

2.
Gutierre M, Telles J, Welling L, Rabelo N, Teixeira M, Figueiredo E . Biomarkers for traumatic brain injury: a short review. Neurosurg Rev. 2020; 44(4):2091-2097. DOI: 10.1007/s10143-020-01421-0. View

3.
Gao F, Wu X, Mao X, Niu F, Zhang B, Dong J . Astaxanthin provides neuroprotection in an experimental model of traumatic brain injury via the Nrf2/HO-1 pathway. Am J Transl Res. 2021; 13(3):1483-1493. PMC: 8014407. View

4.
Papa L, Walter A, Wilkes J, Clonts H, Johnson B, Slobounov S . Effect of Player Position on Serum Biomarkers during Participation in a Season of Collegiate Football. J Neurotrauma. 2022; 39(19-20):1339-1348. PMC: 9529311. DOI: 10.1089/neu.2022.0083. View

5.
Loane D, Stoica B, Faden A . Neuroprotection for traumatic brain injury. Handb Clin Neurol. 2015; 127:343-66. PMC: 4808298. DOI: 10.1016/B978-0-444-52892-6.00022-2. View