Apolipoprotein E4 as a predictor of outcomes in pediatric mild traumatic brain injury

Lisa M Moran1, H Gerry Taylor, Kalaichelvi Ganesalingam

  • 1Department of Psychology, The Ohio State University, Columbus, Ohio, USA.

Journal of Neurotrauma
|August 4, 2009
PubMed

Insights

The apolipoprotein E (APOE) epsilon4 allele did not consistently impact outcomes in children with mild traumatic brain injury (TBI). Further research is needed to understand genetic influences on pediatric TBI recovery.

Area of Science:

  • Neuroscience
  • Genetics
  • Pediatric Traumatology

Background:

  • The apolipoprotein E (APOE) epsilon4 allele is associated with adverse outcomes in adult traumatic brain injury (TBI).
  • Preliminary evidence suggests a similar pattern in pediatric TBI, necessitating further investigation.

Purpose of the Study:

  • To investigate the relationship between the APOE epsilon4 allele and outcomes in children with mild TBI.
  • To assess the impact of the APOE epsilon4 allele on acute injury severity, neuropsychological performance, and post-concussive symptoms in pediatric mild TBI.

Main Methods:

  • Prospective, longitudinal study of 99 children (ages 8-15) with mild TBI.
  • Outcomes assessed acutely and at 2 weeks, 3 months, and 12 months post-injury.
  • Comparison of children with and without the APOE epsilon4 allele on injury severity, neuropsychological tests, and symptom scales.

Main Results:

  • Children with the APOE epsilon4 allele were more likely to have a Glasgow Coma Scale score < 15, but no differences in other injury severity measures.
  • APOE epsilon4 carriers showed better constructional skill performance but no differences in other neuropsychological tests or post-concussive symptoms.
  • No significant demographic differences were observed between children with and without the APOE epsilon4 allele.

Conclusions:

  • The APOE epsilon4 allele does not appear to be consistently related to outcomes in children with mild TBI.
  • Findings suggest the APOE epsilon4 allele's role in pediatric mild TBI may differ from its role in adults or severe TBI.

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