Frontiers in Psychiatry (Apr 2021)

Gene Expression Differences Between Young Adults Based on Trauma History and Post-traumatic Stress Disorder

  • Kaitlin E. Bountress,
  • Vladimir Vladimirov,
  • Vladimir Vladimirov,
  • Gowon McMichael,
  • Z. Nathan Taylor,
  • Gary Hardiman,
  • Dongjun Chung,
  • Zachary W. Adams,
  • Carla Kmett Danielson,
  • Carla Kmett Danielson,
  • Ananda B. Amstadter

DOI
https://doi.org/10.3389/fpsyt.2021.581093
Journal volume & issue
Vol. 12

Abstract

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Background: The purpose of this study was to identify gene expression differences associated with post-traumatic stress disorder (PTSD) and trauma exposure (TE) in a three-group study design comprised of those with and without trauma exposure and PTSD.Methods: We conducted gene expression and gene network analyses in a sample (n = 45) composed of female subjects of European Ancestry (EA) with PTSD, TE without PTSD, and controls.Results: We identified 283 genes differentially expressed between PTSD-TE groups. In an independent sample of Veterans (n = 78) a small minority of these genes were also differentially expressed. We identified 7 gene network modules significantly associated with PTSD and TE (Bonferroni corrected p ≤ 0.05), which at a false discovery rate (FDR) of q ≤ 0.2, were significantly enriched for biological pathways involved in focal adhesion, neuroactive ligand receptor interaction, and immune related processes among others.Conclusions: This study uses gene network analyses to identify significant gene modules associated with PTSD, TE, and controls. On an individual gene level, we identified a large number of differentially expressed genes between PTSD-TE groups, a minority of which were also differentially expressed in the independent sample. We also demonstrate a lack of network module preservation between PTSD and TE, suggesting that the molecular signature of PTSD and trauma are likely independent of each other. Our results provide a basis for the identification of likely disease pathways and biomarkers involved in the etiology of PTSD.

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