Evidence map›Paper›PMID 26271720›Full record

ReviewNeuroscience and biobehavioral reviews2015

Evidence for the role of corticotropin-releasing factor in major depressive disorder.

R Parrish Waters, Marion Rivalan, D A Bangasser, J M Deussing, M Ising, S K Wood, F Holsboer, Cliff H Summers

Abstract readReview
In one paragraph

Review in Neuroscience and biobehavioral reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Suicide Behavior as a Distinct Psychobiology in Major Depression.Advances in experimental medicine and biology · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Major depressive disorder.Nature reviews. Disease primers · 2023
    Review
  17. Article
  18. Article
  19. Article
  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

8 authors at 7 institutions in 2 countries.

R Parrish WatersUniversity of Mary Washington, Fredericksburg, VA, USA. Electronic address: rwaters@umw.edu.
Marion RivalanCharité Universitätsmedizin, Berlin, Germany. Electronic address: marion.rivalan@charite.de.
D A BangasserTemple University, Philadelphia, PA, USA.
J M DeussingMax Planck Institute of Psychiatry, Munich, Germany.
M IsingMax Planck Institute of Psychiatry, Munich, Germany.
S K WoodUniversity of South Carolina School of Medicine, Columbia, SC, USA.
F HolsboerMax Planck Institute of Psychiatry, Munich, Germany; HMNC GmbH, Munich, Germany.
Cliff H SummersUniversity of South Dakota, Vermillion, SD, USA; Sanford School of Medicine, Vermillion, SD, USA. Electronic address: cliff@usd.edu.
Max Planck Institute of Psychiatry · DECharité - Universitätsmedizin Berlin · DEHolsboerMaschmeyer NeuroChemie (Germany) · DETemple University · USUniversity of Mary Washington · USUniversity of South Carolina · USUniversity of South Dakota · US

Funding

Amygdalar Orexin Modulation of Affective DisordersR15MH104485 · NIMH · UNIVERSITY OF SOUTH DAKOTA · PI SUMMERS, CLIFF H · 2015 to 2015
$426k
NIMH NIH HHS R15 MH104485
6 · The paper itself

Abstract

Major depressive disorder (MDD) is a devastating disease affecting over 300 million people worldwide, and costing an estimated 380 billion Euros in lost productivity and health care in the European Union alone. Although a wealth of research has been directed toward understanding and treating MDD, still no therapy has proved to be consistently and reliably effective in interrupting the symptoms of this disease. Recent clinical and preclinical studies, using genetic screening and transgenic rodents, respectively, suggest a major role of the CRF1 gene, and the central expression of CRF1 receptor protein in determining an individual's risk of developing MDD. This gene is widely expressed in brain tissue, and regulates an organism's immediate and long-term responses to social and environmental stressors, which are primary contributors to MDD. This review presents the current state of knowledge on CRF physiology, and how it may influence the occurrence of symptoms associated with MDD. Additionally, this review presents findings from multiple laboratories that were presented as part of a symposium on this topic at the annual 2014 meeting of the International Behavioral Neuroscience Society (IBNS). The ideas and data presented in this review demonstrate the great progress that has been made over the past few decades in our understanding of MDD, and provide a pathway forward toward developing novel treatments and detection methods for this disorder.

Indexed as

Corticotropin-Releasing HormoneCRF Receptor, Type 1HumansMajor Depressive DisorderReceptors, Corticotropin-Releasing HormoneCorticotropin-Releasing HormoneCRF Receptor, Type 1Receptors, Corticotropin-Releasing HormoneCRFCRF(1)DepressionStress

Identifiers

PMID26271720
PMCPMC4828243
OpenAlexW1133363097

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.