The roles of comorbidity and trauma exposure and its timing in shaping HPA axis patterns in depression

PSYCHONEUROENDOCRINOLOGY

卷:120

Article

Mayer, Stefanie E.¹  Peckins, Melissa²  Kuhlman, Kate R.^3,4,5  Rajaram, Nirmala⁶  Lopez-Duran, Nestor L.⁷  Young, Elizabeth A.⁶  Abelson, James L.⁶ 

[1] Univ Calif San Francisco, Dept Psychiat, St,Suite 465, San Francisco, CA 94115 USA

[2] St Johns Univ, Dept Psychol, New York, NY USA

[3] Univ Calif Irvine, Dept Psychol Sci, Irvine, CA USA

[4] Univ Calif Los Angeles, Cousins Ctr Psychoneuroimmunol, Los Angeles, CA USA

[5] Univ Calif Irvine, Inst Interdisciplinary Salivary Biosci, Irvine, CA USA

[6] Univ Michigan, Dept Psychiat, Ann Arbor, MI 48109 USA

[7] Univ Michigan, Dept Psychol, Ann Arbor, MI USA

关键词: HPA;    Depression;    Comorbidity;    Trauma exposure;    Timing of trauma;   

DOI  :  10.1016/j.psyneuen.2020.104776

来源: Elsevier

【 摘 要 】

Background: Much work has documented hypothalamic pituitary adrenal (HPA) axis abnormalities in major depressive disorder (MDD), but inconsistencies leave this system's role in the illness unclear. Comparisons across studies are complicated by variation in co-morbidity (Posttraumatic Stress Disorder-PTSD, anxiety disorders), exposure to trauma, and timing of trauma (child vs. adult). Here, we examined the impact of these factors on HPA axis profiles in depression. Methods: We recruited 5 groups of participants: MDD (n = 14), comorbid MDD + PTSD following adulthood trauma (MDD + PTSD-Adult; n = 12), comorbid MDD + PTSD following childhood trauma (MDD + PTSDChild; n = 18), comorbid MDD + social anxiety disorder (MDD + SAD; n = 12), and non-depressed control participants who were sex and age matched to patients (combined total n = 36). HPA axis function was assessed using three challenges: stress reactivity via the Trier Social Stress Test (TSST), feedback sensitivity via a dexamethasone suppression test (DST), and central drive via a metyrapone challenge (MET). We compared hormonal responses between patient groups and their respective non-depressed controls. Results: MDD + PTSD-Child showed low cortisol levels at baseline, and reduced adrenocorticotropic hormone (ACTH) levels at baseline and throughout the TSST. MDD-only, MDD + PTSD-Adult, and MDD + SAD did not differ from non-depressed controls in HPA axis responses to the TSST. Controlling for childhood trauma severity, the reduced baseline levels in MDD + PTSD-Child were no longer significant and significantly reduced baseline cortisol levels emerged for MDD + PTSD-Adult. No diagnostic group effects were detected with DST and MET. Childhood maltreatment subtypes were associated with unique HPA axis responses to TSST and MET. Conclusion: Comorbidity and trauma exposure, as well as their timing and type, contribute to inconsistencies in the depression literature and must be included in efforts to clarify the role of the HPA axis in MDD.

【 授权许可】

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