Resting-state functional connectivity after hydrocortisone administration in patients with post-traumatic stress disorder and borderline personality disorder

Eur Neuropsychopharmacol. 2019 Aug;29(8):936-946. doi: 10.1016/j.euroneuro.2019.05.008. Epub 2019 Jun 28.

Abstract

In a previous study, we found that - in contrast to healthy individuals - patients with borderline personality disorder (BPD) and post-traumatic stress disorder (PTSD) showed better memory retrieval performance after hydrocortisone administration compared to placebo. As these results suggest an altered function of corticosteroid receptors in the brain in PTSD and BPD, we examined the effect of hydrocortisone on brain activation in both disorders. We recruited 40 female healthy controls, 20 female unmedicated patients with PTSD and 18 female unmedicated patients with BPD. We conducted a placebo-controlled cross-over study, in which all participants underwent two resting state MRI measurements after they received either a placebo or 10 mg hydrocortisone orally and in randomized order. There was a time interval of one week between the measurements. We analysed resting state functional connectivity (RSFC) with the hippocampus and the amygdala as seed regions. Compared to healthy controls, both patient groups showed reduced hippocampus RSFC to dorsomedial prefrontal cortex (dmPFC). Positive hippocampus dmPFC RSFC correlated negatively with childhood trauma (r = -0.47) and with severity of clinical symptoms, measured with the Borderline Symptom List (r = -0.44) and the Posttraumatic Stress Diagnostic Scale (r = -0.45). We found neither differences in amygdala RSFC nor an effect of hydrocortisone administration. Childhood trauma might lead to decreased positive hippocampus dmPFC RSFC. This might explain symptoms of PTSD and BPD that are characterized by dysfunctional fear regulation.

Keywords: Amygdala; Borderline personality disorder; Hippocampus; Hydrocortisone; Posttraumatic stress disorder; Resting state functional connectivity.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Borderline Personality Disorder / diagnostic imaging*
  • Borderline Personality Disorder / physiopathology
  • Brain / diagnostic imaging
  • Brain / drug effects*
  • Brain / physiopathology
  • Brain Mapping
  • Central Nervous System Agents / pharmacology*
  • Cross-Over Studies
  • Female
  • Humans
  • Hydrocortisone / metabolism
  • Hydrocortisone / pharmacology*
  • Magnetic Resonance Imaging
  • Neural Pathways / diagnostic imaging
  • Neural Pathways / physiopathology
  • Rest
  • Saliva / metabolism
  • Stress Disorders, Post-Traumatic / diagnostic imaging
  • Stress Disorders, Post-Traumatic / drug therapy*
  • Stress Disorders, Post-Traumatic / physiopathology

Substances

  • Central Nervous System Agents
  • Hydrocortisone