Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 22, Issue 19, Pages -Publisher
MDPI
DOI: 10.3390/ijms221910865
Keywords
traumatic brain injury; diffuse axonal injury; oxidative stress; reactive oxygen species; biomarkers
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Identifying clinical prognostic factors for diffuse axonal injury (DAI) is crucial, including glycemia, early GCS, oxygen saturation, blood pressure, and time to recover consciousness. Severity of the lesion, based on cerebral anatomical structures involved, is strongly correlated with survival after DAI. Additionally, biomarkers such as GFAP, pNF-H, NF-L, tau, and A beta 42 may be potential targets for future pharmaceutical treatments to prevent DAI-related damages.
Traumatic brain injury (TBI) is a condition burdened by an extremely high rate of morbidity and mortality and can result in an overall disability rate as high as 50% in affected individuals. Therefore, the importance of identifying clinical prognostic factors for diffuse axonal injury (DAI) in (TBI) is commonly recognized as critical. The aim of the present review paper is to evaluate the most recent contributions from the relevant literature in order to understand how each single prognostic factor determinates the severity of the clinical syndrome associated with DAI. The main clinical factors with an important impact on prognosis in case of DAI are glycemia, early GCS, the peripheral oxygen saturation, blood pressure, and time to recover consciousness. In addition, the severity of the lesion, classified on the ground of the cerebral anatomical structures involved after the trauma, has a strong correlation with survival after DAI. In conclusion, modern findings concerning the role of reactive oxygen species (ROS) and oxidative stress in DAI suggest that biomarkers such as GFAP, pNF-H, NF-L, microtubule associated protein tau, A beta 42, S-100 beta, NSE, AQP4, Drp-1, and NCX represent a possible critical target for future pharmaceutical treatments to prevent the damages caused by DAI.
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