Evidence map›Paper›PMID 32306485›Full record

Trial reportDepression and anxiety2020

Neural function during emotion processing and modulation associated with treatment response in a randomized clinical trial for posttraumatic stress disorder.

Elizabeth R Duval, Jony Sheynin, Anthony P King, K Luan Phan, Naomi M Simon, Brian Martis, Katherine E Porter, Sonya B Norman, Israel Liberzon, Sheila A M Rauch

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Depression and anxiety, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.8field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Elizabeth R DuvalVA Ann Arbor Healthcare System, Ann Arbor, Michigan.ORCID 0000-0002-3883-863X
Jony SheyninVA Ann Arbor Healthcare System, Ann Arbor, Michigan.ORCID 0000-0002-8463-2317
Anthony P KingVA Ann Arbor Healthcare System, Ann Arbor, Michigan.ORCID 0000-0002-0764-9625
K Luan PhanDepartment of Psychiatry and Behavioral Health, The Ohio State University, Columbus, Ohio.
Naomi M SimonDepartment of Psychiatry, Massachusetts General Hospital, Boston, Massachusetts.
Brian MartisDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan.
Katherine E PorterVA Ann Arbor Healthcare System, Ann Arbor, Michigan.
Sonya B NormanResearch Service, VA San Diego Healthcare System, San Diego, California.
Israel LiberzonVA Ann Arbor Healthcare System, Ann Arbor, Michigan.
Sheila A M RauchMental Health Service Line, VA Atlanta Healthcare System, Decatur, Georgia.ORCID 0000-0001-9686-4011
University of Michigan · USTexas A&M Health Science Center · USEmory University · USMassachusetts General Hospital · USOhio Department of Health · USUniversity of California San Diego · US

Funding

Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Neural Mechanisms Involved in Contextual Processing in PTSDK23MH109762 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUVAL, ELIZABETH · 2017 to 2021
$759k
NCATS NIH HHS UL1 TR000433NIMH NIH HHS K23 MH109762US Department of Defense Medical Research and Materiel Command W81XWH-11-1-0073
6 · The paper itself

Abstract

backgroundPosttraumatic stress disorder (PTSD) has been associated with exaggerated threat processing and deficits in emotion modulation circuitry. It remains unknown how neural circuits are associated with response to evidence-based treatments for PTSD.

methodWe examined associations between PTSD symptoms and indicators of neural response in key emotion processing and modulation regions. Fifty-six military Veterans with PTSD were randomly assigned to one of three evidence-based treatments (prolonged exposure, sertraline, and PE plus sertraline) in a randomized clinical trial ("PROGrESS"; 2018, Contemp Clin Trials, 64, 128-138). Twenty-seven combat-exposed controls (CCs) served as a comparison group at pretreatment. Before and after PTSD treatment, functional magnetic resonance imaging was used to assess brain activation and connectivity during the validated Shifted Attention Emotion Appraisal Task (2003, J Neurosci, 23, 5627-5633; 2013, Biol Psychiatry, 73, 1045-1053).

resultsGreater activation in emotion processing (anterior insula) and modulation (prefrontal cortex) regions and increased connectivity between attentional control (dorsolateral prefrontal cortex and superior parietal cortex) and emotion processing (amygdala) regions, at pretreatment, were associated with subsequent PTSD symptom improvement.

conclusionsThis study is one of the first to examine task-based activation and functional connectivity in a PTSD treatment trial, and provides evidence to suggest that activation in and connectivity between emotion processing and modulation regions are important predictors of treatment response.

Indexed as

Stress Disorders, Post-TraumaticAmygdalaBrainEmotionsHumansMagnetic Resonance ImagingCognitive Behavioral Therapyfunctional MRIpharmacotherapyPTSDtrauma

Identifiers

PMID32306485
PMCPMC8010611
OpenAlexW3016883955

What OpenQuestion holds

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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.