Repeated mild traumatic brain injuries induce persistent changes in plasma protein and magnetic resonance imaging

David K Wright1,2, Rhys D Brady1,3, Alaa Kamnaksh4

  • 1Department of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia.

Scientific Reports
|October 12, 2019
PubMed

Insights

Repeated mild traumatic brain injury (RmTBI) in rats caused lasting brain abnormalities and cognitive deficits. Advanced MRI and plasma protein analysis show promise as objective biomarkers for RmTBI diagnosis.

Area of Science:

  • Neuroscience
  • Biomarkers
  • Traumatic Brain Injury Research

Background:

  • Single mild traumatic brain injury (mTBI) often results in temporary symptoms.
  • Repeated mild traumatic brain injury (RmTBI) is linked to persistent neurological issues.
  • Objective biomarkers are needed for effective mTBI clinical management due to symptom variability.

Purpose of the Study:

  • To investigate the chronic neurological effects of RmTBI in a rat model.
  • To evaluate advanced magnetic resonance imaging (MRI) and plasma protein levels as potential RmTBI biomarkers.
  • To explore the pathophysiological mechanisms underlying RmTBI-induced abnormalities.

Main Methods:

  • Rats received two mild fluid percussion injuries or sham procedures five days apart.
  • Structural and diffusion-weighted MRI, behavioral tests, and plasma proteomic analysis were performed.
  • Measurements were taken at multiple time points post-injury (days 1, 3, 5, 7, and 30).

Main Results:

  • RmTBI rats exhibited structural and diffusion abnormalities in the cortex and corpus callosum via MRI.
  • Plasma proteomic analysis revealed markers of axonal/vascular injury, metabolic dysfunction, and glial reactivity in RmTBI rats.
  • RmTBI rats displayed persistent cognitive and sensorimotor deficits.

Conclusions:

  • RmTBI can lead to chronic neurological deficits and abnormalities.
  • MRI and plasma protein biomarkers show potential for detecting RmTBI.
  • Findings offer insights into RmTBI's underlying pathophysiological mechanisms.

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