Evidence map›Paper›PMID 36280453›Full record

ArticleBiological psychiatry2023

A Neurobiological Profile Underlying Comorbidity Load and Prospective Increases in Dysphoria in a Focal Fear Sample.

Elizabeth A Bauer, Kayla A Wilson, K Luan Phan, Stewart A Shankman, Annmarie MacNamara

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Amygdala-insula response to neutral stimuli and the prospective prediction of anxiety sensitivity.Progress in neuro-psychopharmacology & biological psychiatry · 2025
    Article
  3. Review
  4. 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

5 authors at 3 institutions in 1 country.

Elizabeth A BauerDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, Texas. Electronic address: eabauer@tamu.edu.
Kayla A WilsonDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, Texas.
K Luan PhanDepartment of Psychiatry and Behavioral Health, Ohio State University, Columbus, Ohio.
Stewart A ShankmanDepartment of Psychiatry and Behavioral Sciences, Northwestern University, Evanston, Illinois.
Annmarie MacNamaraDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, Texas.
Texas A&M University · USNorthwestern University · USThe Ohio State University · US

Funding

HARM-A: A neurobiological predictor of comorbidity and stress reactivity in anxiety disordersR01MH125083 · NIMH · TEXAS A&M UNIVERSITY · PI MACNAMARA, ANNMARIE EILEEN · 2021 to 2025
$3.3M
Brain-Behavior Markers of Negative Affectivity, Comorbidity in Anxiety DisordersK23MH105553 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MACNAMARA, ANNMARIE EILEEN · 2015 to 2018
$648k
NIMH NIH HHS K23 MH105553NIMH NIH HHS R01 MH125083
6 · The paper itself

Abstract

backgroundKnowledge of the neural mechanisms underlying increased disease burden in anxiety disorders that is unaccounted for by individual categorical diagnoses could lead to improved clinical care. Here, we tested the utility of a joint functional magnetic resonance imaging-electroencephalography neurobiological profile characterized by overvaluation of negative stimuli (amygdala) in combination with blunted elaborated processing of these same stimuli (the late positive potential [LPP], an event-related potential) in predicting increased psychopathology across a 2-year period in people with anxiety disorders.

methodsOne hundred ten participants (64 female, 45 male, 1 other) including 78 participants with phobias who varied in the extent of their internalizing comorbidity and 32 participants who were free from psychopathology viewed negative and neutral pictures during separate functional magnetic resonance imaging blood oxygen level-dependent and electroencephalogram recordings. Dysphoria was assessed at baseline and 2 years later.

resultsParticipants with both heightened amygdala activation and blunted LPPs to negative pictures showed the greatest increases in dysphoria 2 years later. Cross-sectionally, participants with higher comorbidity load (≥2 additional diagnoses, n = 34) showed increased amygdala activation to negative pictures compared with participants with lower comorbidity load (≤1 additional diagnosis, n = 44) and compared with participants free from psychopathology. In addition, high comorbid participants showed reduced LPPs to negative pictures compared with low comorbid participants.

conclusionsHeightened amygdala in response to negative stimuli in combination with blunted LPPs could indicate overvaluation of threatening stimuli in the absence of elaborated processing that might otherwise help regulate threat responding. This brain profile could underlie the worsening and maintenance of internalizing psychopathology over time.

Indexed as

BrainFearAnxiety DisordersComorbidityElectroencephalographyEmotionsEvoked PotentialsFemaleHumansMagnetic Resonance ImagingMaleProspective StudiesAmygdalaDysphoriaEmotionEvent-related potentialsLate positive potentialResearch domain criteria

Identifiers

PMID36280453
PMCPMC10866641
OpenAlexW4292241948

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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.