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Post-Traumatic Stress Symptoms after Pediatric Injury: Relation to Pre-Frontal Limbic Circuitry
Linda Ewing-Cobbs1, Dana DeMaster1, Christopher G Watson1
11 Children's Learning Institute and Department of Pediatrics, University of Texas Health Science Center at Houston, Houston, Texas.
Insights
Children with traumatic brain injury (TBI) or extracranial injury (EI) show altered pre-frontal limbic circuitry microstructure. These changes correlate with post-traumatic stress symptoms (PTSS), impacting psychological health.
Area of Science:
- Neuroscience
- Psychology
- Pediatrics
Background:
- Pre-frontal limbic circuitry is susceptible to stress and injury.
- Understanding its microstructural changes post-injury is crucial for child psychological health.
Purpose of the Study:
- To examine pre-frontal limbic circuitry microstructure after traumatic brain injury (TBI) or extracranial injury (EI).
- To investigate the relationship between microstructural alterations and post-traumatic stress symptoms (PTSS) in children.
Main Methods:
- Prospective longitudinal study comparing children with TBI, EI, and healthy controls.
- Diffusion tensor imaging (DTI) and probabilistic tractography to assess white matter microstructure (FA) and gray matter (MD).
- PTSS ratings using a validated scale in injured children.
Main Results:
- Reduced fractional anisotropy (FA) in the right hippocampus to orbital pre-frontal cortex (PFC) pathway in injured versus healthy children.
- Specific PTSS clusters (hyperarousal, avoidance, re-experiencing) positively correlated with higher FA and MD in limbic pathways.
- Age moderated the relationship between microstructure and hyperarousal symptoms.
Conclusions:
- Findings support models implicating disrupted top-down PFC and hippocampal regulation of subcortical threat arousal.
- Alterations in limbic-prefrontal circuitry and PTSS increase risk for current and future psychological problems in children with injuries.
Abstract:
Pre-frontal limbic circuitry is vulnerable to effects of stress and injury. We examined microstructure of pre-frontal limbic circuitry after traumatic brain injury (TBI) or extracranial injury (EI) and its relation to post-traumatic stress symptoms (PTSS). Participants aged 8 to 15 years who sustained mild to severe TBI (n = 53) or EI (n = 26) in motor vehicle incidents were compared with healthy children (n = 38) in a prospective longitudinal study. At the seven-week follow-up, diffusion tensor imaging was obtained in all groups; injured children completed PTSS ratings using a validated scale. Using probabilistic diffusion tensor tractography, pathways were seeded from bilateral amygdalae and hippocampi to estimate the trajectory of white matter connecting them to each other and to targeted pre-frontal cortical (PFC) regions. Microstructure was estimated using fractional anisotropy (FA) in white matter and mean diffusivity (MD) in gray matter. Pre-frontal limbic microstructure was similar across groups, except for reduced FA in the right hippocampus to orbital PFC pathway in the injured versus healthy group. We examined microstructure of components of pre-frontal limbic circuitry with concurrently obtained PTSS cluster scores in the injured children. Neither microstructure nor PTSS scores differed significantly in the TBI and EI groups. Across PTSS factors, specific symptom clusters were related positively to higher FA and MD. Higher hyperarousal, avoidance, and re-experiencing symptoms were associated with higher FA in amygdala to pre-frontal and hippocampus to amygdala pathways. Higher hippocampal MD had a central role in hyperarousal and emotional numbing symptoms. Age moderated the relation of white and gray matter microstructure with hyperarousal scores. Our findings are consistent with models of traumatic stress that implicate disrupted top-down PFC and hippocampal moderation of overreactive subcortical threat arousal systems. Alterations in limbic pre-frontal circuitry and PTSS place children with either brain or body injuries at elevated risk for both current and future psychological health problems.
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