Evidence map›Paper›PMID 26121746›Full record

Trial reportThe Journal of clinical investigation2015

Glucocorticoid receptor antagonism decreases alcohol seeking in alcohol-dependent individuals.

Leandro F Vendruscolo, David Estey, Vivian Goodell, Lauren G Macshane, Marian L Logrip, Joel E Schlosburg, M Adrienne McGinn, Eva R Zamora-Martinez, Joseph K Belanoff, Hazel J Hunt and 5 more

Registry-linked trialOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03548714 (PT150), which is not on this map. Cited by 152 papers.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed
8.1field-weighted citation impact, top 1% 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.

NCT03548714 phase1completednot on this mapstarted 2018, after this paper: background citation

PT150 (Formerly ORG34517) as a Potential Treatment for Alcohol Dependence-Alcohol Interaction Study

TypeinterventionalSponsorPop Test Oncology LLCRan2018 to 2019Enrolled10ConditionsAlcohol Dependence, Alcohol InteractionArmsPT150, Beverage
3 · Its place in the literature

Who cites it

152 citing papers in PubMed, 221 citations in OpenAlex.

  1. Drawbacks to Strengthening Neural Salience Encoding: A Link Between Cortisol and Risky Drinking.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  6. A Phase 2, Double-Blind, Placebo-Controlled Randomized Trial Assessing the Efficacy of ABT-436, a Novel V1b Receptor Antagonist, for Alcohol Dependence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
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92 more citing papers are in PubMed but not listed here.

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

15 authors at 2 institutions in 1 country.

Leandro F Vendruscolo
David Estey
Vivian Goodell
Lauren G Macshane
Marian L Logrip
Joel E Schlosburg
M Adrienne McGinn
Eva R Zamora-Martinez
Joseph K Belanoff
Hazel J Hunt
Pietro P Sanna
Olivier George
George F Koob
Scott Edwards
Barbara J Mason
Scripps Research Institute · USCorcept Therapeutics (United States) · US

Funding

Viral Vector CoreP60AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ERIC P ZORRILLA · 2003 to 2026
$46.3M
Medication Development for Protracted Abstinence in AlcoholismR01AA012602 · NIAAA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MASON, BARBARA J · 1999 to 2016
$10.5M
Gene Network Perturbations in Alcohol Dependence - A Systems BiologyApproachR01AA021667 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI Vez REPUNTE-CANONIGO, PIETRO P SANNA · 2013 to 2026
$6.1M
SYSTEMIC NEUROPHARMACOLOGYP50AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE · PI SANNA, PIETRO P · 1985 to 2002
$5.1M
Alcohol Vapor Self-Administration in RatsR01AA022977 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Olivier George · 2014 to 2026
$5.1M
Glucocorticoid Antagonist Treatment of Alcohol Use DisorderR01AA023152 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MASON, BARBARA J · 2014 to 2018
$2.9M
The Role of Brain Stress Systems in the Prefrontal Cortex in Compulsive DrinkingR01AA020608 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI GEORGE, OLIVIER · 2011 to 2015
$1.8M
Intersection of Pain and Ethanol-Seeking Mechanisms in Ethanol DependenceR00AA020839 · NIAAA · LSU HEALTH SCIENCES CENTER · PI EDWARDS, SCOTT · 2014 to 2016
$739k
Treatment of Opiate Dependence through Inhibition of Fatty Acid Amide HydrolaseK99DA037344 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI SCHLOSBURG, JOEL EVAN · 2014 to 2015
$284k
Intersection of Pain and Ethanol-Seeking Mechanisms in Ethanol DependenceK99AA020839 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI EDWARDS, SCOTT · 2012 to 2013
$274k
NIAAA NIH HHS AA006420NIAAA NIH HHS AA012602NIAAA NIH HHS AA020608NIAAA NIH HHS AA020839NIAAA NIH HHS AA022977NIAAA NIH HHS AA023152NIAAA NIH HHS K99 AA020839NIAAA NIH HHS P50 AA006420NIAAA NIH HHS P60 AA006420NIAAA NIH HHS R00 AA020839NIAAA NIH HHS R01 AA012602NIAAA NIH HHS R01 AA020608NIAAA NIH HHS R01 AA021667NIAAA NIH HHS R01 AA022977NIAAA NIH HHS R01 AA023152NIDA NIH HHS K99 DA037344
6 · The paper itself

Abstract

Alcoholism, or alcohol use disorder, is a major public health concern that is a considerable risk factor for morbidity and disability; therefore, effective treatments are urgently needed. Here, we demonstrated that the glucocorticoid receptor (GR) antagonist mifepristone reduces alcohol intake in alcohol-dependent rats but not in nondependent animals. Both systemic delivery and direct administration into the central nucleus of the amygdala, a critical stress-related brain region, were sufficient to reduce alcohol consumption in dependent animals. We also tested the use of mifepristone in 56 alcohol-dependent human subjects as part of a double-blind clinical and laboratory-based study. Relative to placebo, individuals who received mifepristone (600 mg daily taken orally for 1 week) exhibited a substantial reduction in alcohol-cued craving in the laboratory, and naturalistic measures revealed reduced alcohol consumption during the 1-week treatment phase and 1-week post-treatment phase in mifepristone-treated individuals. Mifepristone was well tolerated and improved liver-function markers. Together, these results support further exploration of GR antagonism via mifepristone as a therapeutic strategy for alcoholism.

Indexed as

Administration, OralAdultAlcohol DrinkingAlcoholismAnimalsFemaleHormone AntagonistsHumansMaleMifepristoneRatsReceptors, GlucocorticoidHormone AntagonistsMifepristoneReceptors, Glucocorticoid

Identifiers

PMID26121746
PMCPMC4563748
OpenAlexW1910403263

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.