Effects of childhood trauma on HPA-axis reactivity in women free of lifetime psychopathology

Exposure to childhood trauma may induce persistent changes in Hypothalamic-Pituitary-Adrenal (HPA)-axis functioning even in the absence of current psychopathology. Because previous studies did not systematically exclude subjects with lifetime psychiatric morbidity, prevalent psychopathology may have...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2009-08, Vol.33 (5), p.889-894
Hauptverfasser: Klaassens, Ellen R., van Noorden, Martijn S., Giltay, Erik J., van Pelt, Johannes, van Veen, Tineke, Zitman, Frans G.
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container_issue 5
container_start_page 889
container_title Progress in neuro-psychopharmacology & biological psychiatry
container_volume 33
creator Klaassens, Ellen R.
van Noorden, Martijn S.
Giltay, Erik J.
van Pelt, Johannes
van Veen, Tineke
Zitman, Frans G.
description Exposure to childhood trauma may induce persistent changes in Hypothalamic-Pituitary-Adrenal (HPA)-axis functioning even in the absence of current psychopathology. Because previous studies did not systematically exclude subjects with lifetime psychiatric morbidity, prevalent psychopathology may have confounded the association. In this study we investigated whether women exposed to childhood trauma, but without a history of psychiatric disorders, show alterations in HPA-axis functioning. We included 10 women exposed to significant childhood trauma and 12 non-exposed women. All women were between 29 and 64 years old, mentally and physically healthy, and without current or lifetime psychopathology. HPA-axis functioning was assessed as 1) basal activity with salivary cortisol patterns over 8 time points on two consecutive sampling days and 2) plasma cortisol and adrenocorticotropic hormone (ACTH) reactivity over 7 time points after the combined dexamethasone/corticotropin-releasing hormone (dex/CRH) challenge test. Basal salivary cortisol output did not differ between trauma-exposed compared to non-exposed women. Significantly blunted plasma cortisol and ACTH responses in response to dex/CRH administration were found in the trauma-exposed compared to the non-exposed women ( F(1,20) = 5.08, p = 0.04 and F(1,20) = 5.23, p = 0.03 respectively). Adjusting for age, body mass index (BMI), oral contraceptive use, and menopausal status, somewhat weakened the associations for cortisol as well as ACTH ( F(1,16) = 3.30, p = 0.09) and F(1,16) = 2.17, p = 0.16 respectively), but for cortisol absolute differences in point estimates were largely unaffected. Although basal cortisol patterns were similar in the two groups, exposure to childhood trauma seemed to be related to a blunted HPA-axis reactivity in women who were free of current or lifetime psychopathology.
doi_str_mv 10.1016/j.pnpbp.2009.04.011
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Because previous studies did not systematically exclude subjects with lifetime psychiatric morbidity, prevalent psychopathology may have confounded the association. In this study we investigated whether women exposed to childhood trauma, but without a history of psychiatric disorders, show alterations in HPA-axis functioning. We included 10 women exposed to significant childhood trauma and 12 non-exposed women. All women were between 29 and 64 years old, mentally and physically healthy, and without current or lifetime psychopathology. HPA-axis functioning was assessed as 1) basal activity with salivary cortisol patterns over 8 time points on two consecutive sampling days and 2) plasma cortisol and adrenocorticotropic hormone (ACTH) reactivity over 7 time points after the combined dexamethasone/corticotropin-releasing hormone (dex/CRH) challenge test. Basal salivary cortisol output did not differ between trauma-exposed compared to non-exposed women. Significantly blunted plasma cortisol and ACTH responses in response to dex/CRH administration were found in the trauma-exposed compared to the non-exposed women ( F(1,20) = 5.08, p = 0.04 and F(1,20) = 5.23, p = 0.03 respectively). Adjusting for age, body mass index (BMI), oral contraceptive use, and menopausal status, somewhat weakened the associations for cortisol as well as ACTH ( F(1,16) = 3.30, p = 0.09) and F(1,16) = 2.17, p = 0.16 respectively), but for cortisol absolute differences in point estimates were largely unaffected. Although basal cortisol patterns were similar in the two groups, exposure to childhood trauma seemed to be related to a blunted HPA-axis reactivity in women who were free of current or lifetime psychopathology.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19389455</pmid><doi>10.1016/j.pnpbp.2009.04.011</doi><tpages>6</tpages></addata></record>
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subjects Adult
Adult and adolescent clinical studies
Adult Survivors of Child Abuse - psychology
Anxiety disorders. Neuroses
Biological and medical sciences
Biomarkers - metabolism
Child clinical studies
Childhood trauma
Cortisol
Dexamethasone-CRH test
Female
HPA-axis
Humans
Hydrocortisone - blood
Hypothalamo-Hypophyseal System - metabolism
Medical sciences
Middle Aged
Miscellaneous
Neuropharmacology
Pharmacology. Drug treatments
Pituitary-Adrenal System - metabolism
Post-traumatic stress disorder
Psychology. Psychoanalysis. Psychiatry
Psychopathology
Psychopathology. Psychiatry
Resilience
Saliva
Saliva - chemistry
Saliva - metabolism
title Effects of childhood trauma on HPA-axis reactivity in women free of lifetime psychopathology
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