Treble-Barna Amery, Patronick Jamie, Uchani Srivatsan, Marousis Noelle C, Zigler Christina K, Fink Ericka L, Kochanek Patrick M, Conley Yvette P, Yeates Keith Owen
Department of Physical Medicine and Rehabilitation, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, United States.
Front Neurol. 2020 Jun 12;11:460. doi: 10.3389/fneur.2020.00460. eCollection 2020.
Unexplained heterogeneity in outcomes following pediatric traumatic brain injury (TBI) is one of the most critical barriers to the development of effective prognostic tools and therapeutics. The addition of personal biological factors to our prediction models may account for a significant portion of unexplained variance and advance the field toward precision rehabilitation medicine. The overarching goal of the Epigenetic Effects on Pediatric Traumatic Brain Injury Recovery (EETR) study is to investigate an epigenetic biomarker involved in both childhood adversity and postinjury neuroplasticity to better understand heterogeneity in neurobehavioral outcomes following pediatric TBI. Our primary hypothesis is that childhood adversity will be associated with worse neurobehavioral recovery in part through an epigenetically mediated reduction in brain-derived neurotrophic factor () expression in response to TBI. EETR is an observational, prospective, longitudinal concurrent cohort study of children aged 3-18 years with either TBI ( = 200) or orthopedic injury ( = 100), recruited from the UPMC Children's Hospital of Pittsburgh. Participants complete study visits acutely and at 6 and 12 months postinjury. Blood and saliva biosamples are collected at all time points-and cerebrospinal fluid (CSF) when available acutely-for epigenetic and proteomic analysis of . Additional measures assess injury characteristics, pre- and postinjury child neurobehavioral functioning, childhood adversity, and potential covariates/confounders. Recruitment began in July 2017 and will occur for ~6 years, with data collection complete by mid-2023. Analyses will characterize DNA methylation and protein levels over the recovery period and investigate this novel biomarker as a potential biological mechanism underlying the known association between childhood adversity and worse neurobehavioral outcomes following pediatric TBI. The study received ethics approval from the University of Pittsburgh Institutional Review Board. Participants and their parents provide informed consent/assent. Research findings will be disseminated via local and international conference presentations and manuscripts submitted to peer-reviewed journals. The study is registered with clinicaltrials.org (ClinicalTrials.gov Identifier: NCT04186429).
小儿创伤性脑损伤(TBI)后结果存在无法解释的异质性,这是开发有效预后工具和治疗方法的最关键障碍之一。在我们的预测模型中加入个人生物学因素,可能会解释很大一部分无法解释的差异,并推动该领域向精准康复医学发展。小儿创伤性脑损伤恢复的表观遗传效应(EETR)研究的总体目标是研究一种涉及儿童期逆境和损伤后神经可塑性的表观遗传生物标志物,以更好地理解小儿TBI后神经行为结果的异质性。我们的主要假设是,儿童期逆境将与较差的神经行为恢复相关,部分原因是表观遗传介导的脑源性神经营养因子(BDNF)表达因TBI而降低。EETR是一项观察性、前瞻性、纵向同期队列研究,研究对象为3至18岁患有TBI(n = 200)或骨科损伤(n = 100)的儿童,从匹兹堡大学医学中心儿童医院招募。参与者在受伤后急性期、6个月和12个月完成研究访视。在所有时间点采集血液和唾液生物样本,急性期如有可用的脑脊液(CSF)也进行采集,用于BDNF的表观遗传和蛋白质组学分析。其他测量指标评估损伤特征、受伤前后儿童的神经行为功能、儿童期逆境以及潜在的协变量/混杂因素。招募工作于2017年7月开始,将持续约6年,数据收集于2023年年中完成。分析将描述恢复期BDNF的DNA甲基化和蛋白质水平,并研究这种新型生物标志物作为儿童期逆境与小儿TBI后较差神经行为结果之间已知关联的潜在生物学机制。该研究获得了匹兹堡大学机构审查委员会的伦理批准。参与者及其父母提供了知情同意/同意书。研究结果将通过在当地和国际会议上发表演讲以及提交给同行评审期刊的手稿进行传播。该研究已在clinicaltrials.org注册(ClinicalTrials.gov标识符:NCT04186429)。