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Harmonization of pipeline for preclinical multicenter plasma protein and miRNA biomarker discovery in a rat model of post-traumatic epileptogenesis.

Authors :
Kamnaksh A
Puhakka N
Ali I
Smith G
Aniceto R
McCullough J
Das Gupta S
Ndode-Ekane XE
Brady R
Casillas-Espinosa P
Hudson M
Santana-Gomez C
Immonen R
Abreu PA
Jones N
Shultz S
Staba RJ
O'Brien TJ
Agoston D
Pitkänen A
Source :
Epilepsy research [Epilepsy Res] 2019 Jan; Vol. 149, pp. 92-101. Date of Electronic Publication: 2018 Nov 26.
Publication Year :
2019

Abstract

The Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) is an international, multicenter, multidisciplinary study aimed at preventing epileptogenesis (EpiBioS4Rx: https://epibios.loni.usc.edu/). One of the study's major objectives is the discovery of diagnostic, prognostic, and predictive plasma protein and microRNA (miRNA) biomarkers that are sensitive, specific, and translatable to the human condition. Epilepsy due to structural brain abnormalities, secondary to neurological insults such as traumatic brain injury (TBI), currently represents ∼50% of all epilepsy cases. In the preclinical EpiBioS4Rx study, TBI was induced in adult male Sprague Dawley rats using a standardized protocol for lateral fluid-percussion injury. Whole blood was collected from the tail vein at baseline and 2, 9 and 30 days post-injury and processed for plasma separation. Biomaterial properties, sample preparation and integrity, and choice of analysis platform can significantly impact measured marker levels and, in turn, interpretation with respect to injury and/or other variables. We present here the results of procedural harmonization for the first 320 rats included in the EpiBioS4Rx study study, from three international research centers, and preliminary proteomic and miRNA analyses. We also discuss experimental considerations for establishing rigorous quality controls with the goal of harmonizing operating procedures across study sites, and delivering high-quality specimens for preclinical biomarker discovery in a rat model of post-traumatic epilepsy (PTE).<br /> (Copyright © 2018 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-6844
Volume :
149
Database :
MEDLINE
Journal :
Epilepsy research
Publication Type :
Academic Journal
Accession number :
30553097
Full Text :
https://doi.org/10.1016/j.eplepsyres.2018.11.009