AI Article Synopsis

  • The study examines the impact of posttraumatic stress disorder (PTSD) on the HPA axis in sexually abused adolescents, noting that previous research has focused less on this age group.
  • Fourteen adolescents with PTSD were compared to fourteen control adolescents, and both groups underwent a dexamethasone suppression test to assess their hormonal responses.
  • Results showed that the PTSD group had significantly lower adrenocorticotropin (ACTH) levels after the test, indicating potential hypersensitivity of their hormone receptors compared to the control group.

Article Abstract

Evidence suggests that individuals with posttraumatic stress disorder (PTSD) have an enhanced sensitization of the hypothalamic--pituitary--adrenocortical (HPA) axis. However, few studies in adolescents have been performed. Fourteen sexually abused adolescent inpatients with DSM-IV PTSD (12 female, two male; mean +/- SD age, 16.2 +/- 1.9 years) were compared with 14 adolescent hospitalized controls (11 female, three male; mean age, 15.7 +/- 2.0 years). All subjects underwent a standard dexamethasone suppression test (DST, 1 mg given orally at 2300 h) five days after admission. Baseline blood samples were obtained at 0800 h, and the following day, adrenocorticotropin (ACTH) and cortisol levels were measured at 0800, 1600, and 2300 h. Clinical assessment included the Impact of Event Scale, Stanford Acute Stress Reaction Questionnaire, Beck Depression Inventory, and Coping Inventory for Stressful Situations. Post-DST ACTH levels were significantly lower in PTSD than in control adolescents (at 0800 h: P < 0.005; at 1600 h: P < 0.001; at 2300 h: P < 0.05). In patients, post-DST cortisol levels were reduced but not significantly. No correlations were found between ACTH and cortisol levels and time elapsed since trauma. These results demonstrate that sexually abused adolescents with PTSD show ACTH hypersuppression to DST suggesting enhanced glucocorticoid receptor sensitivity in the pituitary.

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Source
http://dx.doi.org/10.1016/j.psyneuen.2004.03.006DOI Listing

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