Evidence map›Paper›PMID 27781556›Full record

ReviewExpert review of clinical pharmacology2017

Mood Therapeutics: Novel Pharmacological Approaches for Treating Depression.

Ioline D Henter, Rafael T de Sousa, Philip W Gold, Andre R Brunoni, Carlos A Zarate, Rodrigo Machado-Vieira

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of clinical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Possible Modulatory Role of ARC Gene Variants in Mood Disorders.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2021
    Article
  6. Review
  7. Review
  8. Rapid effects of S-ketamine on the morphology of hippocampal astrocytes and BDNF serum levels in a sex-dependent manner.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2020
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Novel treatment options in depression and psychosis.Neuropsychiatric disease and treatment · 2018
    Review
  15. Review
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

6 authors at 2 institutions in 2 countries.

Ioline D Hentera Experimental Therapeutics and Pathophysiology Branch , NIMH-NIH , Bethesda , Maryland , USA.
Rafael T de Sousaa Experimental Therapeutics and Pathophysiology Branch , NIMH-NIH , Bethesda , Maryland , USA.
Philip W Golda Experimental Therapeutics and Pathophysiology Branch , NIMH-NIH , Bethesda , Maryland , USA.
Andre R Brunonib Laboratory of Neuroscience, LIM- 27, Institute and Department of Psychiatry , University of São Paulo , São Paulo , Brazil.
Carlos A Zaratea Experimental Therapeutics and Pathophysiology Branch , NIMH-NIH , Bethesda , Maryland , USA.
Rodrigo Machado-Vieiraa Experimental Therapeutics and Pathophysiology Branch , NIMH-NIH , Bethesda , Maryland , USA.
National Institutes of Health · USUniversidade de São Paulo · BR

Funding

Target validation of novel therapeutic agents in mood disordersZIAMH002927 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI ZARATE, CARLOS · 2010 to 2025
$37.1M
Intramural NIH HHS ZIA MH002927
6 · The paper itself

Abstract

introductionReal-world effectiveness trials suggest that antidepressant efficacy is limited in many patients with mood disorders, underscoring the urgent need for novel therapeutics to treat these disorders. Areas covered: Here, we review the clinical evidence supporting the use of novel modulators for the treatment of mood disorders, including specific glutamate modulators such as: 1) high-trapping glutamatergic modulators; 2) subunit (NR2B)-specific N-methyl-D-aspartate (NMDA) receptor antagonists; 3) NMDA receptor glycine-site partial agonists; and 4) metabotropic glutamate receptor (mGluR) modulators. We also discuss other promising, non-glutamatergic targets for potential rapid antidepressant effects in mood disorders, including the cholinergic system, the glucocorticoid system, and the inflammation pathway, as well as several additional targets of interest. Clinical evidence is emphasized, and non-pharmacological somatic treatments are not reviewed. In general, this paper only explores agents available in the United States. Expert commentary: Of these novel targets, the most promising - and the ones for whom the most evidence exists - appear to be the ionotropic glutamate receptors. However, moving forward will require us to fully embrace the goal of personalized medicine and will require health professionals to pre-emptively identify potential responders.

Indexed as

Antidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalAntioxidantsCholinergic AntagonistsDepressionExcitatory Amino Acid AgentsHumansAntidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalAntioxidantsCholinergic AntagonistsExcitatory Amino Acid AgentsAMPA receptorbipolar disorderdepressionglutamatemajor depressive disorder (MDD)moodN-methyl-D-aspartate (NMDA)treatment

Identifiers

PMID27781556
PMCPMC5552063
OpenAlexW2542944679

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.