Biomarkers for prediction of chronic traumatic encephalopathy-like pathology following repeated mild traumatic brain injury in rats are partially sex- and age-dependent

Exp Neurol. 2026 Feb:396:115560. doi: 10.1016/j.expneurol.2025.115560. Epub 2025 Nov 14.

Abstract

Introduction: Repeated mild traumatic brain injuries (rmTBIs) pose a high risk of developing chronic traumatic encephalopathy (CTE). Since this neurodegenerative disease is diagnosed only post-mortem, new biomarkers for early detection are needed. Although age at injury and biological sex are important factors in many brain pathologies, little is known about their relevance to rmTBI-induced CTE-like consequences. Hence, this study explored how biological sex and age at the time of impact affect progression and changes in biomarker candidates after experimental rmTBI.

Methods: Rats of both sexes, aged 7 weeks (adolescent) or 14 weeks (adult), were subjected to three mTBIs at 5-day intervals. Neurological, behavioral and cognitive impairments, as well as changes in potential plasma and brain biomarkers, were assessed up to 12 weeks post-injury. The generalized estimating equation model was used to compare sexes and age groups.

Results: RmTBI induced ongoing neurological impairment. While no depressive-like behavior was observed, long-term, age-specific changes in anxiety were observed after rmTBI. A short-term increase in plasma p-tau was found after rmTBI only in male and adolescent rats. Plasma neuron-specific enolase (NSE) levels were elevated in adolescent animals at both 2 weeks and 12 weeks post-rmTBI. An increase in brain neurofibrillary tangles (NFT) was detected 12-weeks after rmTBI. Correlation analyses suggested NSE as a prospective biomarker for anhedonia-like behavior, and brain NFT as an indicator of neurological impairment.

Discussion: We found that behavioral outcomes and biomarker changes following rmTBI in rats were both age- and sex-dependent. This information will help in developing translatable diagnostics to guide CTE treatment in clinical settings.

Keywords: Age; CTE; Concussion; NSE; Sex; Tau; rmTBI.

MeSH terms

  • Age Factors
  • Animals
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Brain / metabolism
  • Brain / pathology
  • Brain Concussion* / complications
  • Brain Concussion* / metabolism
  • Brain Concussion* / pathology
  • Chronic Traumatic Encephalopathy* / etiology
  • Chronic Traumatic Encephalopathy* / metabolism
  • Chronic Traumatic Encephalopathy* / pathology
  • Disease Models, Animal
  • Female
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Sex Characteristics*
  • tau Proteins

Substances

  • Biomarkers
  • tau Proteins