Abstract

BackgroundSexual assault is implicated in several adverse psychological and physical health outcomes, including posttraumatic stress disorder (PTSD) and depression. Neurobiological research has shown variations related to the hypothalamic-pituitary-adrenal (HPA) axis, immune alterations, metabolic function, and brain circuitry. Although these mechanisms have been extensively studied, the results have demonstrated different outcomes in PTSD.MethodsWe compared the plasma adrenocorticotropin (ACTH) and salivary cortisol levels of fifty-eight women with PTSD developed after sexual assault to those of forty-four female controls with no history of trauma. We also evaluated the psychiatric diagnosis and symptom severity of PTSD and depression. The participants’ clinical conditions were associated with their hormonal levels to assess whether symptom severity was related to hormonal imbalance.ResultsA large percentage of sexually assaulted women had PTSD and comorbid depression. The ACTH levels were higher in the PTSD group than the control group and increased as PTSD severity increased, considering depressive symptoms, measured by the Beck Depression Inventory (BDI) (p < 0.0001), as well as PTSD symptoms, measured by subscale D of the Clinician-Administered PTSD Scale (CAPS-5) (p = 0.045) and the CAPS-5 total scale (p = 0.026). Cortisol levels measured at 10 pm were higher for the PTSD group than the control group (p = 0.045, p = 0.037, respectively), and the cortisol awakening response showed elevated cortisol levels for the PTSD group.ConclusionsThese results show a correlation between symptom severity and HPA axis imbalance in patients with PTSD. Elevated ACTH and an elevated cortisol response in patients with comorbid depressive symptoms were the opposite of the expected response for patients with PTSD only. This association leads to the hypothesis that the neurobiological alterations of PTSD are related to the type of symptoms presented and their severity. These manifestations likely influence the disease course, prognosis and response to treatment. These outcomes highlight the need to discuss particular neurobiological alterations in patients with PTSD developed after sexual assault, mainly those with severe depressive symptoms.

Highlights

  • Sexual assault is implicated in several adverse psychological and physical health outcomes, including posttraumatic stress disorder (PTSD) and depression

  • We found an association of adrenocorticotropic hormone (ACTH) levels and higher scores on subscale D of the Clinician-Administered PTSD Scale (CAPS-5) (r = 0.2; p = 0.045), which assesses negative symptoms related to the PTSD diagnosis (Fig. 2)

  • Despite the intrinsic complexity of the neurobiology of PTSD and the multiple factors that may influence it, this study shows a relationship between increased levels of ACTH and the severity of PTSD symptoms, mainly depressive symptoms, in a sample of women recently exposed sexual assault

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Summary

Introduction

Sexual assault is implicated in several adverse psychological and physical health outcomes, including posttraumatic stress disorder (PTSD) and depression. Neurobiological research has shown variations related to the hypothalamic-pituitary-adrenal (HPA) axis, immune alterations, metabolic function, and brain circuitry. These mechanisms have been extensively studied, the results have demonstrated different outcomes in PTSD. Women victims of sexual assault, including rape, report lower perceived health status; more somatic symptoms; more frequent chronic pain complaints; gynaecological syndromes; and psychiatric disorders such as substance abuse, depression, and posttraumatic stress disorder (PTSD) [4,5,6]. Despite the data gathered on the high prevalence of PTSD resulting from this kind of trauma, few studies have addressed the neurobiology of PTSD considering the female population who has experienced sexual violence

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