Corpus Callosum Vasculature Predicts White Matter Microstructure Abnormalities after Pediatric Mild Traumatic Brain

Kara M Wendel1, Jeong Bin Lee2, Bethann M Affeldt2

  • 1Department of Anatomy and Neurobiology, University of California, Irvine School of Medicine, Irvine, California.

Insights

Pediatric mild traumatic brain injury (mTBI) persistently alters white matter (WM) microstructure in the corpus callosum. Increased blood vessel density in the WM following mTBI is linked to these long-term microstructural changes.

Area of Science:

  • Neuroscience
  • Pediatric Traumatic Brain Injury Research
  • White Matter Microstructure

Background:

  • Pediatric traumatic brain injury (TBI) is linked to impaired development and worse outcomes than in adults.
  • The impact of mild TBI (mTBI) on pediatric white matter (WM) microstructure and vascular supply remains unclear.

Purpose of the Study:

  • To investigate the effects of pediatric mTBI on the microstructure and vasculature of the corpus callosum (CC).
  • To determine if alterations in WM vasculature contribute to long-term microstructural changes after pediatric mTBI.

Main Methods:

  • Induced closed-head injury (CHI) mTBI in mice at post-natal day 14.
  • Analyzed corpus callosum (CC) microstructure using diffusion tensor imaging (DTI).
  • Examined myelin, oligodendrocytes, and vasculature using immunohistochemistry (IHC) at 4, 14, and 60 days post-injury.

Main Results:

  • Persistent changes in apparent diffusion coefficient (ADC) in the ipsilateral CC were observed post-mTBI.
  • Minimal changes in myelin and oligodendrocyte densities were found.
  • Vascular features, including vessel density and length, were persistently altered in the ipsilateral CC following mTBI.
  • A strong inverse relationship was found between ADC and vessel density at 60 days post-injury.

Conclusions:

  • Pediatric mTBI leads to long-term microstructural changes in the corpus callosum.
  • WM vasculature alterations, specifically increased vessel density, are implicated in the persistent microstructural changes following pediatric mTBI.

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