Evidence map›Paper›PMID 41643286›Full record

ArticlePsychiatry research. Neuroimaging2026

Local and network neural activations and their associations with sleep parameters during threat conditioning and extinction in persons with generalized anxiety disorder with and without insomnia disorder.

Jeehye Seo, Cagri Yuksel, Katelyn I Oliver, Carolina Daffre, Huijin Song, Natasha B Lasko, Emma R S McCoy, Mohammed R Milad, Byoung-Kyong Min, Edward F Pace-Schott

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In one paragraph

Article in Psychiatry research. Neuroimaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Jeehye SeoLearning Sciences Research Institute, Seoul National University, Seoul, Republic of Korea.
Cagri YukselMcLean Hospital, Belmont, MA, USA; Harvard Medical School, Department of Psychiatry, Boston, MA, USA.
Katelyn I OliverEmory University, Atlanta, GA, USA.
Carolina DaffreDuke University, Durham, NC, USA.
Huijin SongSNUH Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Natasha B LaskoHarvard Medical School, Department of Psychiatry, Boston, MA, USA; Mass General Brigham, Department of Psychiatry, Charlestown MA, USA; Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA, USA.
Emma R S McCoyMcLean Hospital, Belmont, MA, USA.
Mohammed R MiladUniversity of Texas Health Science Center at Houston, McGovern Medical School, Houston TX, USA.
Byoung-Kyong MinLearning Sciences Research Institute, Seoul National University, Seoul, Republic of Korea; Interdisciplinary Program in Neuroscience, Seoul National University, Seoul, Republic of Korea.
Edward F Pace-SchottHarvard Medical School, Department of Psychiatry, Boston, MA, USA; Mass General Brigham, Department of Psychiatry, Charlestown MA, USA; Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA, USA. Electronic address: epace-schott@mgh.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deficient extinction learning and memory are hypothesized mechanisms for pathological anxiety that are associated with sleep disturbance. fMRI neural activations to threat conditioning, extinction learning, and extinction recall were measured. Activations were compared, in persons with Generalized Anxiety Disorder (GAD), between those with moderate to severe Insomnia Disorder (ID) and those with absent or sub-threshold ID. Relationships of activations with measures of sleep quality and physiology were examined. Between-group comparisons and whole-sample correlation with sleep parameters were examined in relation to large-scale brain networks using a liberal cluster-determining threshold. Localized activations were then identified using family-wise error correction. Activations to the reinforced stimulus (CS+) that increased from the beginning to end ("across") threat conditioning were more extensive within the GAD+ID group. Increased activations to the CS+ across extinction learning were greater within the GAD-ID than the GAD+ID group, and delayed 24 h in the latter. Greater sleep efficiency was associated with decreased activations across threat conditioning, but with increased activations across extinction learning. Better sleep quality promoted greater engagement of neural substrates of extinction learning. The GAD+ID group failed to engage brain areas supporting extinction learning immediately following threat conditioning, but did so when stimuli were again presented following a delay.

Indexed as

Anxiety DisordersBrainConditioning, ClassicalExtinction, PsychologicalGeneralized Anxiety DisorderSleepSleep Initiation and Maintenance DisordersAdultBrain MappingFearFemaleHumansMagnetic Resonance ImagingMaleYoung AdultAnxietyArousalAutonomic nervous systemExtinctionFunctional brain imagingGeneralized anxiety disorderInsomnia–comorbidLarge-scale brain networksSleep and psychiatric conditionsThreat conditioning

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Registered trials

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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.