Literature DB >> 15219644

HPA axis activation in major depression and response to fluoxetine: a pilot study.

Elizabeth A Young1, Margaret Altemus, Juan F Lopez, James H Kocsis, Alan F Schatzberg, Charles DeBattista, Jon-Kar Zubieta.   

Abstract

Hypothalamic-pituitary-adrenal (HPA) axis activation is a frequently observed phenomenon in major depression. However, whether this activation has any implications for treatment is unknown. To address this question, we examined baseline response to metyrapone and 6-week response to fluoxetine. Premenopausal women (n = 20) who met criteria for major depression with no other confounding Axis I disorders, medications, or medical illnesses and were not taking hormonal contraceptives were evaluated with an evening metyrapone challenge before the onset of treatment. Twenty-one normal women were also studied with the evening metyrapone challenge. The depressed patients then entered an open label treatment with fluoxetine for 6 weeks. Subjects were classified as responders if they demonstrated a 50% or greater decrease in Hamilton Depression Rating Scale rating. As a group, the depressed women demonstrated significantly increased ACTH secretion compared to control women before the onset of treatment, during the metyrapone challenge. Before treatment, women who were non-responders to fluoxetine showed increased HPA axis activation compared to controls, while the fluoxetine responders did not differ significantly from normal subjects in their ACTH levels during metyrapone challenge. These results suggest that overactivity of the HPA axis may be one factor associated with slower response to fluoxetine. This may reflect the greater severity of subjects with HPA axis dysregulation or the need to normalize the HPA axis with medications for optimal response.

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Year:  2004        PMID: 15219644     DOI: 10.1016/j.psyneuen.2004.02.002

Source DB:  PubMed          Journal:  Psychoneuroendocrinology        ISSN: 0306-4530            Impact factor:   4.905


  25 in total

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

Authors:  Stefanie E Mayer; Melissa Peckins; Kate R Kuhlman; Nirmala Rajaram; Nestor L Lopez-Duran; Elizabeth A Young; James L Abelson
Journal:  Psychoneuroendocrinology       Date:  2020-06-17       Impact factor: 4.905

2.  The GABAergic deficit hypothesis of major depressive disorder.

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Review 4.  Neurosteroid, GABAergic and hypothalamic pituitary adrenal (HPA) axis regulation: what is the current state of knowledge in humans?

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5.  GABAergic control of depression-related brain states.

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Journal:  Adv Pharmacol       Date:  2015-01-14

6.  Antiglucocorticoid therapy for older adults with anxiety and co-occurring cognitive dysfunction: results from a pilot study with mifepristone.

Authors:  Eric J Lenze; Tamara Hershey; John W Newcomer; Jordan F Karp; Daniel Blumberger; Jennifer Anger; Peter Doré; David Dixon
Journal:  Int J Geriatr Psychiatry       Date:  2014-03-14       Impact factor: 3.485

7.  gamma-Aminobutyric acid-type A receptor deficits cause hypothalamic-pituitary-adrenal axis hyperactivity and antidepressant drug sensitivity reminiscent of melancholic forms of depression.

Authors:  Qiuying Shen; Rachnanjali Lal; Beth A Luellen; John C Earnheart; Anne Milasincic Andrews; Bernhard Luscher
Journal:  Biol Psychiatry       Date:  2010-07-01       Impact factor: 13.382

8.  Pretreatment cortisol levels predict posttreatment outcomes among older adults with depression in cognitive behavioral therapy.

Authors:  Jason M Holland; Alan F Schatzberg; Ruth O'Hara; Renee M Marquett; Dolores Gallagher-Thompson
Journal:  Psychiatry Res       Date:  2013-08-14       Impact factor: 3.222

9.  WY14643 produces anti-depressant-like effects in mice via the BDNF signaling pathway.

Authors:  Bo Jiang; Chao Huang; Qing Zhu; Li-Juan Tong; Wei Zhang
Journal:  Psychopharmacology (Berl)       Date:  2014-11-13       Impact factor: 4.530

10.  Effect of aspirin on hypothalamic-pituitary-adrenal function and on neuropsychological performance in healthy adults: a pilot study.

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Journal:  Psychopharmacology (Berl)       Date:  2009-04-29       Impact factor: 4.530

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