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Altered stress system reactivity after pediatric injury: Relation with post-traumatic stress symptoms
Linda Ewing-Cobbs1, Mary R Prasad1, Charles S Cox2
1Department of Pediatrics and Children's Learning Institute, University of Texas Health Science Center at Houston, United States.
Insights
Pediatric injury can alter stress responses. Injured children, especially younger ones, showed altered cortisol levels and dampened reactivity, highlighting a public health concern.
Area of Science:
- Pediatric Psychology
- Neuroendocrinology
- Trauma Studies
Background:
- Childhood injury is a major cause of death and disability.
- Injured children face risks of altered stress responses and post-traumatic stress symptoms (PTSS).
- Understanding biological stress reactivity is crucial for long-term health outcomes.
Purpose of the Study:
- To examine individual differences in stress reactivity of the hypothalamic-pituitary-adrenal (HPA) axis and autonomic nervous system (ANS) post-pediatric injury.
- To identify correlates of HPA axis and ANS stress reactivity with post-traumatic stress symptoms.
- To investigate the relationship between injury type (TBI vs. EI) and stress system responses.
Main Methods:
- Prospective, observational cohort study of hospitalized children (8-15 years) with traumatic brain injury (TBI) or extracranial injury (EI).
- Salivary cortisol and alpha-amylase (sAA) measured before and after the Trier Social Stress Test six months post-injury.
- Comparison with a healthy, non-injured control group.
Main Results:
- Injured children (8-12 yrs) had higher cortisol levels than controls; all injured participants showed dampened cortisol reactivity.
- TBI group had elevated cortisol (children) and sAA (adolescents) compared to the EI group.
- sAA reactivity correlated with PTSS (avoidance in TBI, emotional numbing in EI).
Conclusions:
- Pediatric injury impacts HPA axis and ANS stress reactivity, particularly in younger children.
- Altered biological stress responses are linked to post-traumatic stress symptoms.
- Monitoring biological systems is vital for understanding and managing sequelae across all injury severities.
Abstract:
Injury is the leading cause of death and disability in childhood. Injured children are at high risk for developing alterations in stress response systems and post-traumatic stress symptoms (PTSS) that may compromise long-term physical and psychological health. In a prospective, observational cohort study, we examined individual differences in, and correlates of, stress-reactivity of the hypothalamic-pituitary-adrenal axis (HPA; salivary cortisol) and autonomic nervous system (ANS; salivary alpha amylase, sAA) following pediatric injury. Participants were 8-15 years of age and hospitalized for traumatic brain injury (TBI; n=55; M age=13.9 yrs; 40 males) or extracranial injury (EI; n=29; M age 12.3 yrs, 20 males) following vehicular accidents. Six months post-injury, saliva was collected before and after the Trier Social Stress Test and later assayed for cortisol and sAA. Relative to a healthy non-injured comparison group (n=33; M age=12.5 yrs, 16 males), injured children (ages 8-12 years), but not adolescents (ages 13-15 yrs), had higher cortisol levels; regardless of age, injured participants showed dampened cortisol reactivity to social evaluative threat. Compared to participants with EI, children with TBI had elevated cortisol and adolescents had elevated sAA. With respect to PTSS, individual differences in sAA were negatively correlated with avoidance in the TBI group and positively correlated with emotional numbing within the EI group. Importantly, psychological and neurobiological sequelae were weakly related to injury severity. Given the high prevalence of pediatric injury, these sequelae affect many children and represent a significant public health concern. Consequently, surveillance of post-traumatic sequelae should include the full spectrum of injury severity. Monitoring the activity, reactivity, and regulation of biological systems sensitive to environmental insults may advance our understanding of individual differences in sequelae and adaptation following traumatic pediatric injury.
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