scholarly journals The relationship of parental warm responsiveness and negativity to emerging behavior problems following traumatic brain injury in young children.

2011 ◽  
Vol 47 (1) ◽  
pp. 119-133 ◽  
Author(s):  
Shari L. Wade ◽  
Amy Cassedy ◽  
Nicolay C. Walz ◽  
H. Gerry Taylor ◽  
Terry Stancin ◽  
...  
2018 ◽  
Vol 20 (5) ◽  
pp. 566-576 ◽  
Author(s):  
Karin Reuter-Rice ◽  
Michael Regier ◽  
Ellen Bennett ◽  
Daniel Laskowitz

Background: Pediatric traumatic brain injury (TBI) is a leading cause of death and disability. Polymorphisms in the apolipoprotein E ( APOE) gene have been linked to cerebral vasospasm (CV) and poor outcomes in adults with TBI, yet these associations remain poorly defined in children. Objective: We examined the effect of the relationship between APOE polymorphisms and CV on functional outcomes in children with a TBI. Method: This prospective, descriptive study examined 60 children (aged 10 days to 15 years) with a TBI. Data included demographic information, genetic sampling for the APOE gene and single-nucleotide polymorphisms (SNPs; rs405509, rs429358, rs7412), and daily transcranial Doppler ultrasounds to evaluate for CV. We examined Glasgow Outcome Scale–Extended Pediatrics (GOS-E Peds) scores at the time of discharge and 4–6 weeks after discharge. Results: More than half (56.7%) of the 60 children ( Mage = 5.9 years) were male. Twenty-six participants (43.3%) experienced an occurrence of CV. There were significant differences in injury mechanism (unadjusted p = .048) and age (unadjusted p = .02) between those with and without CV. Also, the noncoding promoter SNP rs405509 T/T, when considered with injury severity, appeared to modify the relationship of APOE genotype to CV. The relationship between APOE and CV had no significant effect on GOS-E Peds scores. Conclusion: Injury severity and the APOE noncoding promoter SNP rs405509 may modify the relationship between APOE and CV in children with TBI. More studies are needed to understand the role of APOE polymorphisms in outcomes in children with TBI.


Brain Injury ◽  
1996 ◽  
Vol 10 (9) ◽  
pp. 663-676 ◽  
Author(s):  
D. GIRARD ◽  
J. BROWN ◽  
M. BURNETT-STOLNACK ◽  
N. HASHIMOTO ◽  
S. HIER-WELLMER ◽  
...  

Neurology ◽  
2017 ◽  
Vol 89 (18) ◽  
pp. 1923-1925 ◽  
Author(s):  
Michael W. Weiner ◽  
Paul K. Crane ◽  
Thomas J. Montine ◽  
David A. Bennett ◽  
Dallas P. Veitch

Traumatic brain injury (TBI) commonly occurs in civilian and military populations. Some epidemiologic studies previously have associated TBI with an increased risk of Alzheimer disease (AD). Recent clinicopathologic and biomarker studies have failed to confirm the relationship of TBI to the development of AD dementia or pathologic changes, and suggest that other neurodegenerative processes might be linked to TBI. Additional studies are required to determine the long-term consequences of TBI.


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