Evidence map›Paper›PMID 28129555›Full record

Trial reportPsychiatry research. Neuroimaging2017

Treatment for social anxiety disorder alters functional connectivity in emotion regulation neural circuitry.

Katherine S Young, Lisa J Burklund, Jared B Torre, Darby Saxbe, Matthew D Lieberman, Michelle G Craske

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychiatry research. Neuroimaging, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  5. Nucleus accumbens volume as a predictor of anxiety symptom improvement following CBT and SSRI treatment in two independent samples.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Trial
  6. Emotion-based brain mechanisms and predictors for SSRI and CBT treatment of anxiety and depression: a randomized trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Trial
  7. Trial
  8. Article
  9. Article
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  12. Neurocircuitry of treatment in anxiety disorders.Biomarkers in neuropsychiatry · 2022
    Article
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  18. 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 at 2 institutions in 1 country.

Katherine S YoungDepartment of Psychology, University of California, 405 Hilgard Avenue, Los Angeles, CA 90095-1563, USA.
Lisa J BurklundDepartment of Psychology, University of California, 405 Hilgard Avenue, Los Angeles, CA 90095-1563, USA.
Jared B TorreDepartment of Psychology, University of California, 405 Hilgard Avenue, Los Angeles, CA 90095-1563, USA.
Darby SaxbeDepartment of Psychology, University of Southern California, Los Angeles, CA, USA.
Matthew D LiebermanDepartment of Psychology, University of California, 405 Hilgard Avenue, Los Angeles, CA 90095-1563, USA.
Michelle G CraskeDepartment of Psychology, University of California, 405 Hilgard Avenue, Los Angeles, CA 90095-1563, USA. Electronic address: craske@psych.ucla.edu.
University of California, Los Angeles · USUniversity of Southern California · US

Funding

Neural mediators of behavior therapy for anxietyR21MH081299 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CRASKE, MICHELLE G · 2008 to 2009
$402k
NIMH NIH HHS R21 MH081299
6 · The paper itself

Abstract

Social anxiety disorder (SAD) is characterized at a neurobiological level by disrupted activity in emotion regulation neural circuitry. Previous work has demonstrated amygdala hyperreactivity and disrupted prefrontal responses to social cues in individuals with SAD (Kim et al., 2011). While exposure-based psychological treatments effectively reduce SAD symptoms, not all individuals respond to treatment. Better understanding of the neural mechanisms involved offers the potential to improve treatment efficacy. In this study, we investigated functional connectivity in emotion regulation neural circuitry in a randomized controlled treatment trial for SAD. Participants with SAD underwent fMRI scanning while performing an implicit emotion regulation task prior to treatment (n=62). Following 12 weeks of cognitive behavioral therapy, acceptance and commitment therapy, or wait-list, participants completed a second scan (n=42). Psychophysiological interaction analyses using amygdala seed regions demonstrated differences between SAD and healthy control participants (HC; n=16) in right amygdala-vmPFC connectivity. SAD participants demonstrated more negative amygdala-to-vmPFC connectivity, compared to HC participants, an effect that was correlated with SAD symptom severity. Post-treatment symptom reduction was correlated with altered amygdala-to-vm/vlPFC connectivity, independent of treatment type. Greater symptom reduction was associated with more negative amygdala-to-vm/vlPFC connectivity. These findings suggest that effective psychological treatment for SAD enhances amygdala-prefrontal functional connectivity.

Indexed as

Cognitive Behavioral TherapyAcceptance and Commitment TherapyAdultAmygdalaEmotionsFemaleHumansMagnetic Resonance ImagingMaleNerve NetPhobia, SocialTreatment OutcomeYoung AdultACTAmygdalaCBTFMRIPrefrontal cortexPsychophysiological interactionsRandomized controlled trial

Identifiers

PMID28129555
PMCPMC5330298
OpenAlexW2577085700

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.