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Epigenetic Effects on Pediatric Traumatic Brain Injury Recovery (EETR): An Observational, Prospective, Longitudinal
Amery Treble-Barna1, Jamie Patronick1, Srivatsan Uchani1
1Department of Physical Medicine and Rehabilitation, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Insights
Childhood adversity may worsen pediatric traumatic brain injury (TBI) recovery by epigenetically reducing brain-derived neurotrophic factor (BDNF). This study investigates BDNF as a biomarker for predicting TBI outcomes in children.
Area of Science:
- Neuroscience
- Genetics
- Pediatrics
Background:
- Pediatric traumatic brain injury (TBI) outcomes show unexplained heterogeneity.
- Childhood adversity is linked to poorer neurobehavioral recovery after TBI.
- Epigenetic factors may mediate the impact of adversity on TBI recovery.
Purpose of the Study:
- To investigate the role of epigenetic modifications of brain-derived neurotrophic factor (BDNF) in pediatric TBI recovery.
- To explore whether childhood adversity influences neurobehavioral outcomes through epigenetically mediated BDNF changes post-TBI.
- To identify potential biomarkers for personalized rehabilitation strategies in pediatric TBI.
Main Methods:
- Prospective, longitudinal cohort study of children aged 3-18 with TBI or orthopedic injury.
- Collection of blood, saliva, and cerebrospinal fluid for epigenetic and proteomic analysis of BDNF.
- Assessment of injury characteristics, neurobehavioral functioning, childhood adversity, and covariates over 12 months post-injury.
Main Results:
- Analysis of BDNF DNA methylation and protein levels throughout the recovery period.
- Investigation of BDNF as a potential mediator between childhood adversity and TBI outcomes.
- Characterization of epigenetic biomarkers for predicting neurobehavioral recovery in pediatric TBI.
Conclusions:
- Epigenetic regulation of BDNF may be a key mechanism linking childhood adversity to TBI recovery.
- BDNF epigenetic markers could improve prognostic accuracy for pediatric TBI.
- Findings may inform precision rehabilitation medicine for children with TBI.
Abstract:
Introduction: 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 (BDNF) expression in response to TBI. Methods and analysis: EETR is an observational, prospective, longitudinal concurrent cohort study of children aged 3-18 years with either TBI (n = 200) or orthopedic injury (n = 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 BDNF. 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 BDNF 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. Ethics and dissemination: 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. Trial Registration: The study is registered with clinicaltrials.org (ClinicalTrials.gov Identifier: NCT04186429).
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