Evidence map›Paper›PMID 30654645›Full record

ArticleThe American journal of psychiatry2019

Altered Uncinate Fasciculus Microstructure in Childhood Anxiety Disorders in Boys But Not Girls.

Do P M Tromp, Lisa E Williams, Andrew S Fox, Jonathan A Oler, Patrick H Roseboom, Gregory M Rogers, Brenda E Benson, Andrew L Alexander, Daniel S Pine, Ned H Kalin

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Review
  9. A preliminary study of the effects of an antimuscarinic agent on anxious behaviors and white matter microarchitecture in nonhuman primates.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  10. Novel mechanism-based treatments for pediatric anxiety and depressive disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Article
  17. The prefrontal cortex, pathological anxiety, and anxiety disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Review
  18. Article
  19. Article
  20. Pediatric PTSD is characterized by age- and sex-related abnormalities in structural connectivity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    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

10 authors at 1 institution in 1 country.

Do P M TrompThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Lisa E WilliamsThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Andrew S FoxThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Jonathan A OlerThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Patrick H RoseboomThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Gregory M RogersThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Brenda E BensonThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Andrew L AlexanderThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Daniel S PineThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Ned H KalinThe Department of Psychiatry (Tromp, Williams, Oler, Roseboom, Rogers, Alexander, Kalin), the Neuroscience Training Program (Tromp, Kalin), the Department of Medical Physics (Alexander), and the HealthEmotions Research Institute (Tromp, Williams, Oler, Roseboom, Kalin), University of Wisconsin, Madison; the Department of Psychology and the California National Primate Research Center, University of California, Davis (Fox); and the Section on Development and Affective Neuroscience, NIMH, Bethesda, Md. (Benson, Pine).
Sherwin Williams (United States) · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
fMRI Studies Of Pediatric Mood And Anxiety DisordersZIAMH002781 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PINE, DANIEL · 2009 to 2025
$41.5M
Fmri Studies Of Risk For Mood And Anxiety Disorders In ChildrenZIAMH002782 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PINE, DANIEL · 2009 to 2025
$28.3M
TRAINING PROGRAM IN EMOTION RESEARCHT32MH018931 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Richard J Davidson · 1989 to 2026
$11.6M
Waisman Intellectual and Developmental Disabilities Research Center Down Syndrome RegistryU54HD090256 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI MESSING, ALBEE · 2016 to 2020
$6.0M
Brain Mechanisms Underlying Childhood Generalized Anxiety DisorderR21MH092581 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI KALIN, NED H · 2012 to 2013
$405k
NICHD NIH HHS U54 HD090256NIH HHS P51 OD011107NIMH NIH HHS R21 MH092581NIMH NIH HHS T32 MH018931
6 · The paper itself

Abstract

objectiveAnxiety disorders are common, can result in lifelong suffering, and frequently begin before adolescence. Evidence from adults suggests that altered prefrontal-limbic connectivity is a pathophysiological feature of anxiety disorders. More specifically, in adults with anxiety disorders, decreased fractional anisotropy (FA), a measure of white matter integrity, has been observed in the uncinate fasciculus, the major tract that connects limbic and prefrontal regions. Because of the early onset of anxiety disorders and the increased incidence in anxiety disorders in females during their reproductive years, it is important to understand whether the reduction in uncinate fasciculus FA exists in children with anxiety disorders and the extent to which this alteration is sex related. To address these issues, the authors assessed FA in the uncinate fasciculus in unmedicated boys and girls with anxiety disorders.

methodsFA measures were derived from diffusion tensor images that were acquired from 98 unmedicated children (ages 8-12); 52 met criteria for generalized anxiety disorder, separation anxiety disorder, social anxiety disorder, or anxiety disorder not otherwise specified, and 46 were matched control subjects.

resultsTract-based results demonstrated that children with anxiety disorders have significant reductions in uncinate fasciculus FA. A significant sex-by-group interaction and post hoc testing revealed that this effect was evident only in boys. No other main effects or sex-by-group interactions were found for other white matter tracts.

conclusionsThese findings provide evidence of uncinate fasciculus white matter alterations in boys with anxiety disorders. The data demonstrate that anxiety disorder-related alterations in prefrontal-limbic structural connectivity are present early in life, are not related to psychotropic medication exposure, and are sex specific. Building on these findings, future research has the potential to provide insights into the genesis and sexual dimorphism of the pathophysiology that leads to anxiety disorders, as well as to identify sex-specific early-life treatment targets.

Indexed as

Anxiety DisordersCase-Control StudiesChildDiffusion Tensor ImagingFemaleFrontal LobeFunctional NeuroimagingHumansMaleNeural PathwaysPrefrontal CortexSex FactorsWhite MatterAnxiety Disorder-GeneralizedBiological Markers

Identifiers

PMID30654645
PMCPMC6661168
OpenAlexW2909971369

What OpenQuestion holds

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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.