Evidence map›Paper›PMID 30207258›Full record

ArticlePsychological medicine2019

Linking genes, circuits, and behavior: network connectivity as a novel endophenotype of externalizing.

Naomi Sadeh, Jeffrey M Spielberg, Mark W Logue, Jasmeet P Hayes, Erika J Wolf, Regina E McGlinchey, William P Milberg, Steven A Schichman, Annjanette Stone, Mark W Miller

Open access · greenAbstract read
In one paragraph

Article in Psychological medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Validity and utility of Hierarchical Taxonomy of Psychopathology (HiTOP): II. Externalizing superspectrum.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2021
    Article
  5. Article
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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

10 authors at 5 institutions in 1 country.

Naomi SadehDepartment of Psychological and Brain Sciences,University of Delaware,Newark, DE,USA.
Jeffrey M SpielbergDepartment of Psychological and Brain Sciences,University of Delaware,Newark, DE,USA.
Mark W LogueNational Center for PTSD,Behavioral Science Division,VA Boston Healthcare System,Boston, MA,USA.
Jasmeet P HayesNational Center for PTSD,Behavioral Science Division,VA Boston Healthcare System,Boston, MA,USA.
Erika J WolfNational Center for PTSD,Behavioral Science Division,VA Boston Healthcare System,Boston, MA,USA.
Regina E McGlincheyTranslational Research Center for TBI and Stress Disorders and Geriatric Research, Educational and Clinical Center, VA Boston Healthcare System,Boston, MA,USA.
William P MilbergTranslational Research Center for TBI and Stress Disorders and Geriatric Research, Educational and Clinical Center, VA Boston Healthcare System,Boston, MA,USA.
Steven A SchichmanPharmacogenomics Analysis Laboratory,Research Service, Central Arkansas Veterans Healthcare System,Little Rock, AR,USA.
Annjanette StonePharmacogenomics Analysis Laboratory,Research Service, Central Arkansas Veterans Healthcare System,Little Rock, AR,USA.
Mark W MillerNational Center for PTSD,Behavioral Science Division,VA Boston Healthcare System,Boston, MA,USA.
VA Boston Healthcare System · USBoston University · USCentral Arkansas Veterans Healthcare System · USNational Center for PTSD · USUniversity of Delaware · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI BERNICE PORJESZ · 1989 to 2026
$162.7M
Updated confocal microscope in the Imaging Core facility to support biomedical researchP20GM103653 · NIGMS · DELAWARE STATE UNIVERSITY · PI HARRINGTON, MELISSA A · 2012 to 2022
$22.7M
Vivarium CoreP30GM145765 · NIGMS · DELAWARE STATE UNIVERSITY · PI MELISSA A HARRINGTON · 2022 to 2026
$7.7M
Neuroimaging Genetics of PTSDR21MH102834 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MILLER, MARK W · 2014 to 2015
$355k
NIAAA NIH HHS U10 AA008401NIGMS NIH HHS P20 GM103653NIGMS NIH HHS P30 GM145765NIMH NIH HHS R21 MH102834
6 · The paper itself

Abstract

backgroundExternalizing disorders are known to be partly heritable, but the biological pathways linking genetic risk to the manifestation of these costly behaviors remain under investigation. This study sought to identify neural phenotypes associated with genomic vulnerability for externalizing disorders.

methodsOne-hundred fifty-five White, non-Hispanic veterans were genotyped using a genome-wide array and underwent resting-state functional magnetic resonance imaging. Genetic susceptibility was assessed using an independently developed polygenic score (PS) for externalizing, and functional neural networks were identified using graph theory based network analysis. Tasks of inhibitory control and psychiatric diagnosis (alcohol/substance use disorders) were used to measure externalizing phenotypes.

resultsA polygenic externalizing disorder score (PS) predicted connectivity in a brain circuit (10 nodes, nine links) centered on left amygdala that included several cortical [bilateral inferior frontal gyrus (IFG) pars triangularis, left rostral anterior cingulate cortex (rACC)] and subcortical (bilateral amygdala, hippocampus, and striatum) regions. Directional analyses revealed that bilateral amygdala influenced left prefrontal cortex (IFG) in participants scoring higher on the externalizing PS, whereas the opposite direction of influence was observed for those scoring lower on the PS. Polygenic variation was also associated with higher Participation Coefficient for bilateral amygdala and left rACC, suggesting that genes related to externalizing modulated the extent to which these nodes functioned as communication hubs.

conclusionsFindings suggest that externalizing polygenic risk is associated with disrupted connectivity in a neural network implicated in emotion regulation, impulse control, and reinforcement learning. Results provide evidence that this network represents a genetically associated neurobiological vulnerability for externalizing disorders.

Indexed as

EndophenotypesInhibition, PsychologicalAdultAmygdalaConnectomeCorpus StriatumEmotional RegulationExecutive FunctionFemaleGenetic Predisposition to DiseaseGyrus CinguliHippocampusHumansImpulsive BehaviorMagnetic Resonance ImagingMaleAlcohol usedisinhibitionneural circuitspolygenic risk scoresubstance use

Identifiers

PMID30207258
PMCPMC6414280
OpenAlexW2892009114

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.