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Updated: Aug 31, 2025

Murine Model of Controlled Cortical Impact for the Induction of Traumatic Brain Injury
Published on: August 16, 2019
Novel Psychiatric Disorder 6 Months After Traumatic Brain Injury in Children and Adolescents
Jeffrey E Max1, Imogen Drake1, Florin Vaida1
1Department of Psychiatry (Max), Division of Biostatistics & Bioinformatics, Herbert Wertheim School of Public Health (Vaida), and Department of Radiology (Hesselink), University of California, San Diego; Rady Children's Hospital, San Diego (Max); Taconic Hills High School, Craryville, New York (Drake); University of Texas Health Science Center at Houston (Ewing-Cobbs, Saunders); The Hospital for Sick Children, University of Toronto(Schachar); Center for BrainHealth, The University of Texas at Dallas (Chapman); Department of Psychology, Brigham Young University, Provo, Utah (Bigler); Department of Neurology, University of Utah, Salt Lake City (Bigler, Wilde); Department of Psychiatry and Behavioral Sciences (Yang) and Department of Radiology and Biomedical Imaging (Tymofiyeva), University of California, San Francisco; Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, Houston (Wilde, Levin).
Insights
Pediatric traumatic brain injury (TBI) can lead to new psychiatric disorders. Frontal lobe lesions, specifically in white matter and certain gyri, independently predict these adverse outcomes in children.
Area of Science:
- Neuroscience
- Child Psychiatry
- Neurology
Background:
- Traumatic brain injury (TBI) in children can have long-term consequences.
- The development of new psychiatric disorders post-TBI is a significant concern.
- Understanding predictive factors is crucial for early intervention.
Purpose of the Study:
- To identify predictors of new psychiatric disorders within six months after pediatric TBI.
- To explore the role of biopsychosocial factors and specific brain lesion locations.
Main Methods:
- Recruited 177 children (ages 5-14) hospitalized for TBI.
- Assessed pre-injury characteristics, including psychiatric history, SES, and psychosocial factors.
- Utilized MRI to identify lesion locations and assessed psychiatric outcomes at six months.
Main Results:
- 58 out of 141 children (41%) developed new psychiatric disorders.
- Lower SES, higher psychosocial adversity, and frontal lobe lesions were associated with new disorders.
- Frontal lobe white matter, superior frontal gyrus, and orbital gyrus lesions were independent predictors.
Conclusions:
- New psychiatric disorders are common after pediatric TBI.
- While psychosocial factors play a role, specific frontal lobe lesion locations are independent predictors.
- Targeting interventions based on lesion location may be beneficial.
Objective:
To investigate the factors predictive of novel psychiatric disorders in the interval 0-6 months following traumatic brain injury (TBI).
Methods:
Children ages 5-14 years consecutively hospitalized for mild to severe TBI at five hospitals were recruited. Participants were evaluated at baseline (soon after injury) for pre-injury characteristics including psychiatric disorders, socioeconomic status (SES), psychosocial adversity, family function, family psychiatric history, and adaptive function. In addition to the psychosocial variables, injury severity and lesion location detected with acquisition of a research MRI were measured to develop a biopsychosocial predictive model for development of novel psychiatric disorders. Psychiatric outcome, including occurrence of a novel psychiatric disorder, was assessed 6 months after the injury.
Results:
The recruited sample numbered 177 children, and 141 children (80%) returned for the six-month assessment. Of the 141 children, 58 (41%) developed a novel psychiatric disorder. In univariable analyses, novel psychiatric disorder was significantly associated with lower SES, higher psychosocial adversity, and lesions in frontal lobe locations, such as frontal white matter, superior frontal gyrus, inferior frontal gyrus, and orbital gyrus. Multivariable analyses found that novel psychiatric disorder was independently and significantly associated with frontal-lobe white matter, superior frontal gyrus, and orbital gyrus lesions.
Conclusion:
The results demonstrate that occurrence of novel psychiatric disorders following pediatric TBI requiring hospitalization is common and has identifiable psychosocial and specific biological predictors. However, only the lesion predictors were independently related to this adverse psychiatric outcome.
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