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Traumatic brain injury (TBI) presents a major global health concern, characterized by a variety of negative long-term neurological outcomes. Current diagnostic tools lack the sensitivity to fully capture the complex pathophysiology of TBI and predict long-term consequences, underscoring the need for robust methods for biomarker detection. This study, conducted within the multicenter Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) framework, used a standardized lateral fluid-percussion injury (FPI) model to produce TBI in the left hemisphere of adult male Sprague-Dawley rats across three sites: University of Eastern Finland, Monash University, and the University of California, Los Angeles. This study utilized a novel kernel regression method for improved estimation of fiber orientations and streamline tractography to derive diffusion tensor imaging (DTI) metrics of 36 white matter tracts which were used as features to classify TBI versus sham-operated rodents scanned at 2 days (30 sham, 87 TBI), 9 days (29 sham, 84 TBI), 1 month (28 sham, 81 TBI), and 5 months (25 sham, 65 TBI) post-injury using elastic net regression regularization. A mean area under the curve (AUC) of 0.92 was achieved in correctly classifying the TBI rats in a leave-one-out cross-validation (LOOCV) framework. The results revealed delayed, region-specific effects on the microstructure of the left fimbria and left thalamic subcortical projections at 5 months following TBI. By integrating multi-compartment modeling, tractography, and harmonization, this study advances our understanding of the temporal evolution of TBI pathogenesis, paving the way for development of translational prognostic biomarkers for the risk of post-traumatic epilepsy (PTE).
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http://dx.doi.org/10.1162/imag_a_00471 | DOI Listing |
AJNR Am J Neuroradiol
September 2025
From the Department of Department of Radiology, Massachusetts General Hospital, Boston, MA, United States.
Background And Purpose: Low-level light therapy (LLLT) has been shown to modulate recovery in patients with traumatic brain injury (TBI). However, the longitudinal impact of LLLT on brain metabolites has not been studied. The purpose of this study was to use magnetic resonance spectroscopic imaging (MRSI) to assess the metabolic response of LLLT in patients with moderate TBI at acute (within 1 week), subacute (2-3 weeks), and late-subacute (3 months) recovery phases.
View Article and Find Full Text PDFExp Neurol
September 2025
CNRS UMR 5536 RMSB, University of Bordeaux, Bordeaux, France; Basic Science Department, Loma Linda University School of Medicine, Loma Linda, CA, USA; CNRS UMR 7372 CEBC, La Rochelle University, Villiers-en-Bois, France.
Introduction: The vulnerability of white matter (WM) in acute and chronic moderate-severe traumatic brain injury (TBI) has been established. In concussion syndromes, including preclinical rodent models, lacking are comprehensive longitudinal studies spanning the mouse lifespan. We previously reported early WM modifications using clinically relevant neuroimaging and histological measures in a model of juvenile concussion at one month post injury (mpi) who then exhibited cognitive deficits at 12mpi.
View Article and Find Full Text PDFCrit Care Explor
September 2025
Surgical Services, Minneapolis VA Medical Center, Minneapolis, MN.
Objective: This post hoc study of the Progesterone for Traumatic Brain Injury, Experimental Clinical Treatment (ProTECT) III trial investigates whether improving traumatic brain injury (TBI) classification, using serum biomarkers (glial fibrillary acidic protein [GFAP] and ubiquitin carboxyl-terminal esterase L1 [UCH-L1]) and algorithmically assessed total lesion volume, could identify a subset of responders to progesterone treatment, beyond broad measures like the Glasgow Coma Scale (GCS) and Glasgow Outcome Scale-Extended (GOS-E), which may fail to capture subtle changes in TBI recovery.
Design: Brain lesion volumes on CT scans were quantified using Brain Lesion Analysis and Segmentation Tool for CT. Patients were classified into true-positive and true-negative groups based on an optimization scheme to determine a threshold that maximizes agreement between radiological assessment and objectively measured lesion volume.
Front Neurol
August 2025
UCLA Brain Injury Research Center, Department of Neurosurgery, Geffen Medical School, University of California at Los Angeles, Los Angeles, CA, United States.
Multi-site neuroimaging studies have become increasingly common in order to generate larger samples of reproducible data to answer questions associated with smaller effect sizes. The data harmonization model NeuroCombat has been shown to remove site effects introduced by differences in site-related technical variance while maintaining group differences, yet its effect on improving statistical power in pre-clinical models of CNS disease is unclear. The present study examined fractional anisotropy data computed from diffusion weighted imaging data at 3 and 30 days post-controlled cortical impact injury from 184 adult rats across four sites as part of the Translational-Outcome-Project-in-Neurotrauma (TOP-NT) Consortium.
View Article and Find Full Text PDFJ Craniofac Surg
August 2025
Department of Neurosurgery, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University.
Objective: To explore the effects of bone marrow stem cell (BMSC)-derived exosome miR-30a/DLL4 expression on angiogenesis following traumatic brain injury (TBI), which may provide a novel therapeutic strategy for postoperative TBI recovery.
Methods: A rat TBI model was established using the free-fall method, and exosomes from different sources were injected into the brain. Rats were divided into sham-operated, TBI model, TBI+inhibitor NC-Exo, TBI+miR-30a-inhibitor-Exo, TBI+OE NC-Exo, and TBI+DLL4-OE-Exo groups.