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Does Processing Speed Mediate the Effect of Pediatric Traumatic Brain Injury on Working Memory?
  • Published Date:
    Jul 27 2015
  • Source:
    Neuropsychology. 30(3):263-273.
Filetype[PDF - 183.51 KB]


Details:
  • Pubmed ID:
    26214659
  • Pubmed Central ID:
    PMC4729671
  • Description:
    Objective

    Processing speed (PS) and working memory (WM), core abilities that support learning, are vulnerable to disruption following traumatic brain injury (TBI). Developmental increases in WM are related to age-related changes in PS. The purpose of this study was to investigate whether WM deficits in children with TBI are mediated by PS.

    Method

    The performance of children with complicated-mild, moderate, and severe TBI (n=77) was examined relative to an orthopedic injury (n=30) and a healthy comparison group (n=40) an average of 4 years after injury (range 8 months to 12 years). Coding was utilized as a measure of PS, while the WM measures included complex verbal and visual-spatial span tasks with parallel processing requirements. Mediation analysis examined whether TBI might have an indirect effect on WM through PS.

    Results

    Children in the TBI group performed more poorly than the combined comparison groups on Coding and visual-spatial WM. Verbal WM scores were lower in TBI and the healthy comparison relative to the orthopedic group. TBI severity group differences were found on Coding, but not WM measures. The relation between Coding and both the WM tasks was similar. Bootstrap regression analyses suggested that PS, as measured by Coding, might partially mediate the effect of group performance on WM.

    Conclusions

    TBI disrupts core PS and WM abilities that scaffold more complex abilities. Importantly, slowed PS was associated with WM deficits commonly identified following pediatric TBI. Implications of our findings regarding the relation between PS and WM may suggest interventions for children and adolescents following TBI.

  • Document Type:
  • Collection(s):
  • Funding:
    R01 NS046308/NS/NINDS NIH HHS/United States
    U01 CE002188/CE/NCIPC CDC HHS/United States
    UL1 TR000371/TR/NCATS NIH HHS/United States
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