Evidence map›Paper›PMID 28848413›Full record

ArticleFrontiers in human neuroscience2017

Disrupted Working Memory Circuitry in Adolescent Psychosis.

Ariel Eckfeld, Katherine H Karlsgodt, Kristen M Haut, Peter Bachman, Maria Jalbrzikowski, Jamie Zinberg, Theo G M van Erp, Tyrone D Cannon, Carrie E Bearden

Open access · goldAbstract read
In one paragraph

Article in Frontiers in human neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 4 institutions in 1 country.

Ariel EckfeldDepartment of Psychology, UCLALos Angeles, CA, United States.
Katherine H KarlsgodtDepartment of Psychology, UCLALos Angeles, CA, United States.
Kristen M HautDepartment of Psychiatry, Rush University Medical CenterChicago, IL, United States.
Peter BachmanDepartment of Psychiatry, University of PittsburghPittsburgh, PA, United States.
Maria JalbrzikowskiDepartment of Psychiatry, University of PittsburghPittsburgh, PA, United States.
Jamie ZinbergSemel Institute for Neuroscience and Human Behavior, UCLALos Angeles, CA, United States.
Theo G M van ErpDepartment of Psychiatry and Human Behavior, University of California, IrvineIrvine, CA, United States.
Tyrone D CannonDepartments of Psychology and Psychiatry, Yale UniversityNew Haven, CT, United States.
Carrie E BeardenDepartment of Psychology, UCLALos Angeles, CA, United States.
University of Pittsburgh · USRush University Medical Center · USUniversity of California, Irvine · USYale University · US

Funding

UCLA Center for Translational Research in Neurodevelopment: UC-TRaNU54HD087101 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCCRACKEN, JAMES T. · 2016 to 2020
$6.5M
Working Memory and Social Functioning in SchizophreniaR01MH065079 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CANNON, TYRONE D · 2003 to 2007
$2.7M
Cognitive Neuroscience of the Psychosis ProdromeK23MH087708 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NIENDAM, TARA ANN · 2010 to 2014
$784k
NICHD NIH HHS U54 HD087101NIMH NIH HHS K23 MH087708NIMH NIH HHS R01 MH065079
6 · The paper itself

Abstract

Individuals with schizophrenia (SZ) consistently show deficits in spatial working memory (WM) and associated atypical patterns of neural activity within key WM regions, including the dorsolateral prefrontal cortex (dlPFC) and parietal cortices. However, little research has focused on adolescent psychosis (AP) and potential age-associated disruptions of WM circuitry that may occur in youth with this severe form of illness. Here we utilized each subject's individual spatial WM capacity to investigate task-based neural dysfunction in 17 patients with AP (16.58 ± 2.60 years old) as compared to 17 typically developing, demographically comparable adolescents (18.07 ± 3.26 years old). AP patients showed lower behavioral performance at higher WM loads and lower overall WM capacity compared to healthy controls. Whole-brain activation analyses revealed greater bilateral precentral and right postcentral activity in controls relative to AP patients, when controlling for individual WM capacity. Seed-based psychophysiological interaction (PPI) analyses revealed significantly greater co-activation between the left dlPFC and left frontal pole in controls relative to AP patients. Significant group-by-age interactions were observed in both whole-brain and PPI analyses, with AP patients showing atypically greater neural activity and stronger coupling between WM task activated brain regions as a function of increasing age. Additionally, AP patients demonstrated positive relationships between right dlPFC neural activity and task performance, but unlike healthy controls, failed to show associations between neural activity and out-of-scanner neurocognitive performance. Collectively, these findings are consistent with atypical WM-related functioning and disrupted developmental processes in youth with AP.

Indexed as

adolescenceconnectivitydevelopmentschizophreniaworking memory capacity

Identifiers

PMID28848413
PMCPMC5550407
OpenAlexW2744303279

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.