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miRNA dysregulation in traumatic brain injury and epilepsy: a systematic review to identify putative biomarkers for post-traumatic epilepsy

Journal

METABOLIC BRAIN DISEASE
Volume -, Issue -, Pages -

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11011-023-01172-z

Keywords

Epilepsy; Post-traumatic epilepsy; Traumatic brain injury; Micro-RNA; Signaling pathway; Biomarker

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Traumatic brain injury (TBI) and post-traumatic epilepsy (PTE) share similar molecular mechanisms, and dysregulation of microRNAs (miRNAs) in both conditions has been reported. This systematic review analyzed research articles and database studies to identify commonly dysregulated miRNAs in TBI and epilepsy. The study found 85 and 222 dysregulated miRNAs in TBI and epilepsy respectively, with 10 miRNAs commonly dysregulated. These findings may help identify potential biomarkers for PTE.
Traumatic brain injury (TBI) leads to post-traumatic epilepsy (PTE); hence, both TBI and PTE share various similar molecular mechanisms. MicroRNA (miRNA) is a small noncoding RNA that acts as a gene-silencing molecule. Notably, the dysregulation of miRNAs in various neurological diseases, including TBI and epilepsy, has been reported in several studies. However, studies on commonly dysregulated miRNAs and the regulation of shared pathways in both TBI and epilepsy that can identify potential biomarkers of PTE are still lacking. This systematic review covers the peer-review publications of TBI and database studies of epilepsy-dysregulated miRNAs of clinical studies. For TBI, 290 research articles were identified after screening, and 12 provided data for dysregulated miRNAs in humans. The compiled data suggest that 85 and 222 miRNAs are consecutively dysregulated in TBI and epilepsy. In both, 10 miRNAs were found to be commonly dysregulated, implying that they are potentially dysregulated miRNAs for PTE. Furthermore, the targets and involvement of each putative miRNA in different pathways were identified and evaluated. Additionally, clusters of predicted miRNAs were analyzed. Each miRNA's regulatory role was linked with apoptosis, inflammation, and cell cycle regulation pathways. Hence, these findings provide insight for future diagnostic biomarkers.

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