Evidence map›Paper›PMID 40133425›Full record

Trial reportMolecular psychiatry2025

Effects of KCNQ potassium channel modulation on ventral tegmental area activity and connectivity in individuals with depression and anhedonia.

Laurel S Morris, Sara Costi, Sara Hameed, Katherine A Collins, Emily R Stern, Avijit Chowdhury, Carole Morel, Ramiro Salas, Dan V Iosifescu, Ming-Hu Han and 2 more

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

12 authors.

Laurel S MorrisDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA. laurel.morris@mssm.edu.ORCID 0000-0002-5862-6650
Sara CostiDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA.
Sara HameedDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA.
Katherine A CollinsNathan Kline Institute, Orangeburg, NY, USA.
Emily R SternNathan Kline Institute, Orangeburg, NY, USA.
Avijit ChowdhuryDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA.
Carole MorelDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, USA.ORCID 0000-0002-5076-1938
Ramiro SalasMenninger Department of Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-1105-566X
Dan V IosifescuNathan Kline Institute, Orangeburg, NY, USA.
Ming-Hu HanDepartment of Mental Health and Public Health, Faculty of Life and Health Sciences, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong, PR China.
Sanjay J MathewMenninger Department of Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-2715-6641
James W MurroughDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA. james.murrough@mssm.edu.ORCID 0000-0001-6286-1242

Funding

Developing Neuronal KCNQ Channel Modulators for Mood DisordersR61MH111932 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MURROUGH, JAMES WARREN · 2017 to 2018
$1.6M
CSRD VA I01 CX001937U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R61MH111932
6 · The paper itself

Abstract

Up to half of individuals with depression do not respond to first-line treatments, possibly due to a lack of treatment interventions informed by neurobiology. A novel therapeutic approach for depression has recently emerged from translational work targeting aberrant activity of ventral tegmental area (VTA) dopamine neurons via modulation of the KCNQ voltage-gated potassium channels. In this study, individuals with major depressive disorder (MDD) with elevated anhedonia were randomized to five weeks of the KCNQ channel opener, ezogabine (up to 900 mg/day) or placebo. Participants completed functional MRI during a monetary anticipation task and resting-state at baseline and at end-of-treatment. The clinical results were reported previously. Here, we examined VTA activity during monetary anticipation and resting-state functional connectivity between the VTA and the ventromedial prefrontal cortex (mesocortical pathway) and ventral striatum (mesolimbic pathway) at baseline and end-of-treatment. Results indicated a significant drug-by-time interaction in VTA activation during anticipation (F

Indexed as

AnhedoniaKCNQ Potassium ChannelsVentral Tegmental AreaAdultCarbamatesDepressionDopaminergic NeuronsDouble-Blind MethodFemaleHumansMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedNeural PathwaysPhenylenediaminesCarbamatesezogabineKCNQ Potassium ChannelsPhenylenediamines

Identifiers

What OpenQuestion holds

Textmetadata
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.