Evidence map›Paper›PMID 34843625›Full record

ArticleDepression and anxiety2022

Longitudinal hippocampal circuit change differentiates persistence and remission of pediatric posttraumatic stress disorder.

Grace C George, Taylor J Keding, Sara A Heyn, Ryan J Herringa

Open access · greenAbstract read
In one paragraph

Article in Depression and anxiety, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 11 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

4 authors at 1 institution in 1 country.

Grace C GeorgeNeuroscience & Public Policy Program, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0001-6700-9964
Taylor J KedingNeuroscience Training Program, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-0507-6712
Sara A HeynDepartment of Psychiatry, BRAVE Youth Lab, Madison, Wisconsin, USA.ORCID 0000-0003-0907-1342
Ryan J HerringaNeuroscience Training Program, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-1936-7959
University of Wisconsin–Madison · US

Funding

University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
Neurobehavioral mechanisms of parent-child extinction learning in adolescent PTSDR01MH117141 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI HERRINGA, RYAN J · 2019 to 2023
$3.7M
Normative and atypical trajectories of cognitive-emotional development in adolescenceR01MH115910 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI HERRINGA, RYAN J · 2018 to 2023
$3.3M
Neural Basis of Emotion Regulation in Pediatric Post-traumatic Stress DisorderK08MH100267 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI HERRINGA, RYAN J · 2014 to 2018
$990k
NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1 TR002373NIMH NIH HHS K08 MH100267NIMH NIH HHS R01 MH115910NIMH NIH HHS R01 MH117141
6 · The paper itself

Abstract

backgroundPrevious studies have identified functional brain abnormalities in pediatric posttraumatic stress disorder (pPTSD) suggesting altered frontoparietal-subcortical function during emotion processing. However, little is known about how the brain functionally changes over time in recovery versus the persistence of pPTSD.

methodsThis longitudinal study recruited 23 youth with PTSD and 28 typically developing (TD) youth (ages: 8.07-17.99). Within the PTSD group, nine remitted by the 1-year follow-up (Remit) while the remaining 14 persisted (PTSD). At each visit, youth completed an emotional processing task in which they viewed threat and neutral images during functional magnetic resonance imaging (fMRI). Voxelwise activation analyses using linear mixed-effects regression were conducted using a group (TD, Remit, PTSD) by time (baseline, follow-up) by valence (threat, neutral) design. Based on activation findings, a subsequent analysis of hippocampal functional connectivity was performed using a similar model.

resultsPTSD youth showed significantly increasing hippocampal activation to threatening images compared to TD youth, while the Remit group showed more similar patterns to TD youth. Subsequent hippocampal functional connectivity analyses reveal the Remit group showed increasing functional connectivity between the hippocampus and visual cortex (V4) while viewing threat stimuli.

conclusionsThese findings represent one of the first preliminary reports of functional brain substrates of persistence and remission in pPTSD. Notably, increased hippocampal activation to threat and decreased connectivity in the hippocampal-V4 network over time may contribute to persistence in pPTSD. These findings suggest potential biomarkers that could be utilized to advance the treatment of pediatric PTSD.

Indexed as

Stress Disorders, Post-TraumaticAdolescentBrain MappingChildHippocampusHumansLongitudinal StudiesMagnetic Resonance Imagingadolescenceemotionfunctional magnetic resonance imagingneurodevelopmentposttraumatic stress disorderremission

Identifiers

PMID34843625
PMCPMC8763137
OpenAlexW3214785488

What OpenQuestion holds

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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.