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创伤后癫痫发生大鼠模型中临床前多中心血浆蛋白和miRNA生物标志物发现流程的协调统一

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

作者信息

Kamnaksh Alaa, Puhakka Noora, Ali Idrish, Smith Gregory, Aniceto Roxanne, McCullough Jesse, Das Gupta Shalini, Ndode-Ekane Xavier Ekolle, Brady Rhys, Casillas-Espinosa Pablo, Hudson Matt, Santana-Gomez Cesar, Immonen Riikka, Abreu Pedro Andrade de, Jones Nigel, Shultz Sandy, Staba Richard J, O'Brien Terence J, Agoston Denes, Pitkänen Asla

机构信息

Department of Anatomy, Physiology and Genetics, Uniformed Services University, Maryland, USA.

A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.

出版信息

Epilepsy Res. 2019 Jan;149:92-101. doi: 10.1016/j.eplepsyres.2018.11.009. Epub 2018 Nov 26.

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).

摘要

癫痫抗癫痫发生治疗生物信息学研究(EpiBioS4Rx)是一项国际多中心多学科研究,旨在预防癫痫发生(EpiBioS4Rx:https://epibios.loni.usc.edu/)。该研究的主要目标之一是发现对人类情况敏感、特异且可转化应用的诊断、预后和预测性血浆蛋白及微小RNA(miRNA)生物标志物。由结构性脑异常引起的癫痫,继发于诸如创伤性脑损伤(TBI)等神经损伤,目前约占所有癫痫病例的50%。在临床前的EpiBioS4Rx研究中,使用标准化的侧方流体冲击伤方案在成年雄性Sprague Dawley大鼠中诱导TBI。在基线以及损伤后2天、9天和30天从尾静脉采集全血并进行处理以分离血浆。生物材料特性、样品制备与完整性以及分析平台的选择会显著影响所测标志物水平,进而影响对损伤和/或其他变量的解读。我们在此展示了来自三个国际研究中心的EpiBioS4Rx研究纳入的前320只大鼠的程序协调结果,以及初步的蛋白质组学和miRNA分析。我们还讨论了为在创伤后癫痫(PTE)大鼠模型中建立严格质量控制以协调各研究地点的操作程序并提供用于临床前生物标志物发现的高质量标本的实验考量。

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