Evidence map›Paper›PMID 26462618›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

How Administration of the Beta-Blocker Propranolol Before Extinction can Prevent the Return of Fear.

Marijn C W Kroes, Klodiana-Daphne Tona, Hanneke E M den Ouden, Susanne Vogel, Guido A van Wingen, Guillén Fernández

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 5 pooled it
2.8field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 5 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Acute stress leaves fear generalization in healthy individuals intact.Cognitive, affective & behavioral neuroscience · 2021
    Trial
  8. Role of Human Ventromedial Prefrontal Cortex in Learning and Recall of Enhanced Extinction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Trial
  9. Review
  10. Article
  11. Article
  12. Review
  13. Rewarded Extinction Increases Amygdalar Connectivity and Stabilizes Long-Term Memory Traces in the vmPFC.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  14. Article
  15. Review
  16. Memory ModulationFrontiers in human neuroscience · 2022
    Article
  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

6 authors at 1 institution in 1 country.

Marijn C W KroesDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Klodiana-Daphne TonaDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Hanneke E M den OudenDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Susanne VogelDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Guido A van WingenDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Guillén FernándezDonders Institute for Brain, Cognition, and Behaviour, Donders Centre for Cognitive Neuroimaging, Radboud University, Nijmegen, The Netherlands.
Radboud University Nijmegen · NL

Funding

European Research Council 268800
6 · The paper itself

Abstract

Combining beta-blockers with exposure therapy has been advocated to reduce fear, yet experimental studies combining beta-blockers with memory reactivation have had contradictory results. We explored how beta-blockade might affect the course of safety learning and the subsequent return of fear in a double-blind placebo-controlled functional magnetic resonance imaging study in humans (N=46). A single dose of propranolol before extinction learning caused a loss of conditioned fear responses, and prevented the subsequent return of fear and decreased explicit memory for the fearful events in the absence of drug. Fear-related neural responses were persistently attenuated in the dorsal medial prefrontal cortex (dmPFC), increased in the hippocampus 24 h later, and correlated with individual behavioral indices of fear. Prediction error-related responses in the ventral striatum persisted during beta-blockade. We suggest that this pattern of results is most consistent with a model where beta-blockade can prevent the return of fear by (i) reducing retrieval of fear memory, via the dmPFC and (ii) increasing contextual safety learning, via the hippocampus. Our findings suggest that retrieval of fear memory and contextual safety learning form potential mnemonic target mechanisms to optimize exposure-based therapy with beta-blockers.

Indexed as

Adrenergic beta-AntagonistsBrainDouble-Blind MethodExtinction, PsychologicalFearFemaleFunctional NeuroimagingHippocampusHumansMagnetic Resonance ImagingMaleMemoryPrefrontal CortexPropranololAdrenergic beta-AntagonistsPropranolol

Identifiers

PMID26462618
PMCPMC4820039
OpenAlexW2273859401

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.