Evidence map›Paper›PMID 30782974›Full record

Trial reportThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Role of Human Ventromedial Prefrontal Cortex in Learning and Recall of Enhanced Extinction.

Joseph E Dunsmoor, Marijn C W Kroes, Jian Li, Nathaniel D Daw, Helen B Simpson, Elizabeth A Phelps

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04468360 (Facilitation of Extinction Retention and Reconsolidation Blockade by IV Allopregnanolone in PTSD- Pharmacokinetic Studies), which is not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
–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.

NCT04468360 phase2terminatednot on this mapstarted 2022, after this paper: background citation

Facilitation of Extinction Retention and Reconsolidation Blockade by IV Allopregnanolone in PTSD- Pharmacokinetic Studies

TypeinterventionalSponsorBoston UniversityRan2022 to 2025Enrolled11ConditionsPharmacokinetic Study, Post Traumatic Stress DisorderArmsPK-1 Good Manufacturing Practices (GMP) allopregnanolone (Allo) with Dexolve in 0.9% saline for infusion manufactured by the University of California, Davis, PK-2 GMP allopregnanolone (Allo) with Dexolve in 0.9% saline for infusion manufactured by the University of California, Davis.
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  19. Latent-state and model-based learning in PTSD.Trends in neurosciences · 2024
    Review
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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.

Joseph E DunsmoorDepartment of Psychiatry, University of Texas at Austin, Austin, Texas 78712, joseph.dunsmoor@austin.utexas.edu.ORCID 0000-0002-5448-6873
Marijn C W KroesDepartment of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.ORCID 0000-0002-5329-9566
Jian LiSchool of Psychological and Cognitive Sciences and Beijing Key Laboratory of Behaviour and Mental Health, Peking University, Beijing, China.ORCID 0000-0002-3941-2622
Nathaniel D DawPrinceton Neuroscience Institute and Department of Psychology, Peking University, Princeton, New Jersey 08544.ORCID 0000-0001-5029-1430
Helen B SimpsonDepartment of Psychiatry, Columbia University, New York, New York 10032.
Elizabeth A PhelpsDepartment of Psychology, Harvard University, Cambridge, Massachusetts 02138.ORCID 0000-0001-9604-4611

Funding

Preventing the return of fear in humans: Reconsolidation and controlR01MH097085 · NIMH · NEW YORK UNIVERSITY · PI PHELPS, ELIZABETH ANYA · 2012 to 2016
$1.9M
Supplement to: Improving the Control of Fear: Healthy Adults to Pathological AnxietyR00MH106719 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI DUNSMOOR, JOSEPH EDWARD · 2017 to 2019
$883k
NIMH NIH HHS R00 MH106719NIMH NIH HHS R01 MH097085
6 · The paper itself

Abstract

Standard fear extinction relies on the ventromedial prefrontal cortex (vmPFC) to form a new memory given the omission of threat. Using fMRI in humans, we investigated whether replacing threat with novel neutral outcomes (instead of just omitting threat) facilitates extinction by engaging the vmPFC more effectively than standard extinction. Computational modeling of associability (indexing surprise strength and dynamically modulating learning rates) characterized skin conductance responses and vmPFC activity during novelty-facilitated but not standard extinction. Subjects who showed faster within-session updating of associability during novelty-facilitated extinction also expressed better extinction retention the next day, as expressed through skin conductance responses. Finally, separable patterns of connectivity between the amygdala and ventral versus dorsal mPFC characterized retrieval of novelty-facilitated versus standard extinction memories, respectively. These results indicate that replacing threat with novel outcomes stimulates vmPFC involvement on extinction trials, leading to a more durable long-term extinction memory.

Indexed as

AdolescentAdultConditioning, ClassicalExtinction, PsychologicalFearFemaleFunctional NeuroimagingGalvanic Skin ResponseHumansLearningMagnetic Resonance ImagingMaleMental RecallModels, NeurologicalPrefrontal CortexRetention, PsychologyextinctionfMRIinhibitory learningPavlovian conditioningventromedial prefrontal cortex

Identifiers

PMID30782974
PMCPMC6788822

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.