Evidence map›Paper›PMID 36684686›Full record

ArticleFrontiers in rehabilitation sciences2022

Frontoamygdala hyperconnectivity predicts affective dysregulation in adolescent moderate-severe TBI.

Kevin C Bickart, Alexander Olsen, Emily L Dennis, Talin Babikian, Ann N Hoffman, Aliyah Snyder, Christopher A Sheridan, Jesse T Fischer, Christopher C Giza, Meeryo C Choe and 1 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in rehabilitation sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06073886 (Personalized Circuit-Based Frontoamygdala Neuromodulation for Persistent Post-Concussive Symptoms), which is not on this map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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.

NCT06073886 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Personalized Circuit-Based Frontoamygdala Neuromodulation for Persistent Post-Concussive Symptoms

TypeinterventionalSponsorUniversity of California, Los AngelesRan2024 to 2027Enrolled75ConditionsPost-Concussion Syndrome, Concussion, Brain, Mild Traumatic Brain Injury, Head InjuryArmsActive cTBS, Inactive/Sham cTBS, Imaginal exposure
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. 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

11 authors at 5 institutions in 2 countries.

Kevin C BickartBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Alexander OlsenDepartment of Psychiatry and Biobehavioral Sciences, UCLA, Los Angeles, CA, United States.
Emily L DennisTBI and Concussion Center, Department of Neurology, University of Utah, Salt Lake City, UT, United States.
Talin BabikianBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Ann N HoffmanBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Aliyah SnyderBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Christopher A SheridanWake Forest School of Medicine, Radiology Informatics and Image Processing Laboratory, Winston-Salem, NC, United States.
Jesse T FischerBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Christopher C GizaBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Meeryo C ChoeBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Robert F AsarnowBrainSPORT, Department of Neurosurgery, UCLA, Los Angeles, CA, United States.
Neurobehavioral Systems · USMattel Children's Hospital · USNorwegian University of Science and Technology · NOUniversity of Utah · USWake Forest University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In survivors of moderate to severe traumatic brain injury (msTBI), affective disruptions often remain underdetected and undertreated, in part due to poor understanding of the underlying neural mechanisms. We hypothesized that limbic circuits are integral to affective dysregulation in msTBI. To test this, we studied 19 adolescents with msTBI 17 months post-injury (TBI: M age 15.6, 5 females) as well as 44 matched healthy controls (HC: M age 16.4, 21 females). We leveraged two previously identified, large-scale resting-state (rsfMRI) networks of the amygdala to determine whether connectivity strength correlated with affective problems in the adolescents with msTBI. We found that distinct amygdala networks differentially predicted externalizing and internalizing behavioral problems in patients with msTBI. Specifically, patients with the highest medial amygdala connectivity were rated by parents as having greater externalizing behavioral problems measured on the BRIEF and CBCL, but not cognitive problems. The most correlated voxels in that network localize to the rostral anterior cingulate (rACC) and posterior cingulate (PCC) cortices, predicting 48% of the variance in externalizing problems. Alternatively, patients with the highest ventrolateral amygdala connectivity were rated by parents as having greater internalizing behavioral problems measured on the CBCL, but not cognitive problems. The most correlated voxels in that network localize to the ventromedial prefrontal cortex (vmPFC), predicting 57% of the variance in internalizing problems. Both findings were independent of potential confounds including ratings of TBI severity, time since injury, lesion burden based on acute imaging, demographic variables, and other non-amygdalar rsfMRI metrics (e.g., rACC to PCC connectivity), as well as macro- and microstructural measures of limbic circuitry (e.g., amygdala volume and uncinate fasciculus fractional anisotropy). Supporting the clinical significance of these findings, patients with msTBI had significantly greater externalizing problem ratings than healthy control participants and all the brain-behavior findings were specific to the msTBI group in that no similar correlations were found in the healthy control participants. Taken together, frontoamygdala pathways may underlie chronic dysregulation of behavior and mood in patients with msTBI. Future work will focus on neuromodulation techniques to directly affect frontoamygdala pathways with the aim to mitigate such dysregulation problems.

Indexed as

affective dysregulationamygdalabehavioral dysregulationfrontoamygdalamoderate to severe TBIresting-state fMRI

Identifiers

PMID36684686
PMCPMC9845889
OpenAlexW4313585610

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.