4.6 Article

Brain-Based Biotypes of Psychiatric Vulnerability in the Acute Aftermath of Trauma

Journal

AMERICAN JOURNAL OF PSYCHIATRY
Volume 178, Issue 11, Pages 1037-1049

Publisher

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2021.20101526

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Funding

  1. AstraZeneca
  2. Roche Diagnostics
  3. Takeda
  4. Verily
  5. Florida Medical Malpractice Joint Underwriter's Association's Dr. Alvin E. Smith Safety of Healthcare Services
  6. NIH/National Institute on Aging Jacksonville Aging Studies Center [R33AG05654]
  7. Florida Blue Foundation
  8. NIH [R01HD079076, R03HD094577]
  9. Eunice Kennedy Shriver National Institute of Child Health and Human Development
  10. National Center for Medical Rehabilitation Research
  11. Mayday Fund, NIMH [U01 MH110925, K00 MH119603, K01 MH118467]
  12. One Mind Foundation
  13. U.S. Army Medical Research and Material Command
  14. Alkermes
  15. BrainsWay
  16. Genomind

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This study conducted a longitudinal investigation of trauma exposure and mental health outcomes, identifying different neural activity profiles reflecting threat reactivity, reward reactivity, and inhibitory engagement shortly after trauma. The findings revealed clusters with different longitudinal patterns of posttrauma symptoms, suggesting potential neuroimaging-based biotypes of trauma resilience and psychopathology.
Objective: Major negative life events, such as trauma exposure, can play a key role in igniting or exacerbating psychopathology. However, few disorders are diagnosed with respect to precipitating events, and the role of these events in the unfolding of new psychopathology is not well understood. The authors conducted a multisite transdiagnostic longitudinal study of trauma exposure and related mental health outcomes to identify neurobiological predictors of risk, resilience, and different symptom presentations. Methods: A total of 146 participants (discovery cohort: N=69; internal replication cohort: N=77) were recruited from emergency departments within 72 hours of a trauma and followed for the next 6 months with a survey, MRI, and physiological assessments. Results: Task-based functional MRI 2 weeks after a motor vehicle collision identified four clusters of individuals based on profiles of neural activity reflecting threat reactivity, reward reactivity, and inhibitory engagement. Three clusters were replicated in an independent sample with a variety of trauma types. The clusters showed different longitudinal patterns of posttrauma symptoms. Conclusions: These findings provide a novel characterization of heterogeneous stress responses shortly after trauma exposure, identifying potential neuroimaging-based biotypes of trauma resilience and psychopathology.

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