Evidence map›Paper›PMID 19133699›Full record

ReviewDepression and anxiety2009

Glucocorticoid inhibition in the treatment of depression: can we think outside the endocrine hypothalamus?

Mitchel A Kling, Victoria H Coleman, Jay Schulkin

Open access · greenAbstract readReview
In one paragraph

Review in Depression and anxiety, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
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  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Mifepristone modulates serotonin transporter function.Neural regeneration research · 2014
    Article
  13. Review
  14. Article
  15. A CRHR1 haplotype moderates the effect of adverse childhood experiences on lifetime risk of major depressive episode in African-American women.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2011
    Article
  16. Article
  17. Review
  18. Article
  19. Hormone treatment of depression.Dialogues in clinical neuroscience · 2011
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Mitchel A KlingDepartment of Clinical Translational Medicine, Wyeth Research, Collegeville, Pennsylvania, USA.
Victoria H Coleman
Jay Schulkin
American Congress of Obstetricians and Gynecologists · USPhiladelphia VA Medical Center · US

Funding

THE NEUROBIOLOGY OF UNIPOLAR DEPRESSIONZ01MH002659 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI GOLD, PHILIP W · 1993 to 2008
$940k
Intramural NIH HHS Z01 MH002659
6 · The paper itself

Abstract

backgroundMajor depressive disorder affects a substantial percentage of the U.S. population, and can be highly debilitating. Selective serotonin reuptake inhibitors are commonly prescribed to treat depression, but may not be as effective for more severe or persistent depression.

methodsThe authors review data concerning the effects of corticosteroid synthesis inhibitors (CSIs) in the management of depressive disorders, present a hypothesis as to their possible mechanisms of action based on recent data suggesting synergistic effects of glucocorticoids on extrahypothalamic corticotropin-releasing hormone (CRH), and consider alternative hypotheses. Published reports evaluating the efficacy of CSIs in treating depression are reviewed and presented in light of recent findings regarding actions of glucocorticoids on the central CRH system.

resultsResults from open label and double-blind studies by several groups have indicated that CSIs may be efficacious or of adjunctive value in some patients with depression, including those refractory to other agents; however, there is a need for more controlled studies. Several lines of data suggest that the mechanism of action of these agents may not be solely a function of inhibition of adrenal cortisol production.

conclusionsThe authors propose that CSIs may be efficacious in part by reducing glucocorticoid enhancement of CRH action in neurons of the central nucleus of the amygdala and other structures outside the endocrine hypothalamus. Possible effects of systemically administered CSIs on glucocorticoid receptor regulation, neuroactive steroids, and classical monoamine systems are also discussed. We conclude that available clinical data suggest a potential role for CSIs in the management of depressive disorders, especially major depression with psychotic features.

Indexed as

Adrenal GlandsAminoglutethimideAnti-Inflammatory AgentsCorticotropin-Releasing HormoneDouble-Blind MethodGlucocorticoidsHumansHydrocortisoneHypothalamusKetoconazoleMajor Depressive DisorderMetyraponeMifepristoneSeverity of Illness IndexAminoglutethimideAnti-Inflammatory AgentsCorticotropin-Releasing HormoneGlucocorticoidsHydrocortisoneKetoconazoleMetyraponeMifepristone

Identifiers

PMID19133699
PMCPMC3640810
OpenAlexW2007018171

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.