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Journal Article

Citation

Hicks SD, Olympia RP, Onks C, Kim RY, Zhen KJ, Fedorchak G, DeVita S, Rangnekar A, Heller M, Zwibel H, Monteith C, Gagnon Z, McLoughlin CD, Randall J, Madeira M, Campbell TR, Fengler E, Dretsch MN, Neville C, Middleton FA. Int. J. Mol. Sci. 2020; 21(20): e7758.

Copyright

(Copyright © 2020, Molecular Diversity Preservation International)

DOI

10.3390/ijms21207758

PMID

33092191

Abstract

Recurrent concussions increase risk for persistent post-concussion symptoms, and may lead to chronic neurocognitive deficits. Little is known about the molecular pathways that contribute to persistent concussion symptoms. We hypothesized that salivary measurement of microribonucleic acids (miRNAs), a class of epitranscriptional molecules implicated in concussion pathophysiology, would provide insights about the molecular cascade resulting from recurrent concussions. This hypothesis was tested in a case-control study involving 13 former professional football athletes with a history of recurrent concussion, and 18 age/sex-matched peers. Molecules of interest were further validated in a cross-sectional study of 310 younger individuals with a history of no concussion (n = 230), a single concussion (n = 56), or recurrent concussions (n = 24). There was no difference in neurocognitive performance between the former professional athletes and their peers, or among younger individuals with varying concussion exposures. However, younger individuals without prior concussion outperformed peers with prior concussion on three balance assessments. Twenty salivary miRNAs differed (adj. p < 0.05) between former professional athletes and their peers. Two of these (miR-28-3p and miR-339-3p) demonstrated relationships (p < 0.05) with the number of prior concussions reported by younger individuals. miR-28-3p and miR-339-5p may play a role in the pathophysiologic mechanism involved in cumulative concussion effects.


Language: en

Keywords

biomarker; mild traumatic brain injury; microRNA; saliva; sports-related concussion

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