Evidence map›Paper›PMID 32512402›Full record

ArticleNeuroImage. Clinical2020

Adolescents at clinical high risk for psychosis show qualitatively altered patterns of activation during rule learning.

Joseph M Orr, Jesus Lopez, Michael J Imburgio, Andrea Pelletier-Baldelli, Jessica A Bernard, Vijay A Mittal

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. 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 58% 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, 2 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

Joseph M OrrDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, TX, United States; Texas A&M Institute for Neuroscience, Texas A&M University, College Station, TX, United States. Electronic address: joseph.orr@tamu.edu.
Jesus LopezDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, TX, United States. Electronic address: jesusjlopez619@tamu.edu.
Michael J ImburgioDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, TX, United States. Electronic address: mimburgi@tamu.edu.
Andrea Pelletier-BaldelliDepartment of Psychiatry, UNC-Chapel Hill School of Medicine, Chapel Hill, NC, United States. Electronic address: andrea_baldelli@med.unc.edu.
Jessica A BernardDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, TX, United States; Texas A&M Institute for Neuroscience, Texas A&M University, College Station, TX, United States. Electronic address: jessica.bernard@tamu.edu.
Vijay A MittalDepartment of Psychiatry, Northwestern University, Evanston, IL, United States; Medical Social Sciences, Northwestern University, Evanston, IL, United States; Institute for Policy Research (IPR), Northwestern University, Evanston, IL, United States; Institute for Innovations in Developmental Sciences (DevSci), Northwestern University, Evanston, IL, United States. Electronic address: vijay.mittal@northwestern.edu.
Texas A&M University · USNorthwestern University · USUniversity of North Carolina at Chapel Hill · US

Funding

Frontal-Subcortical Development, Movement Abnormalities, and Risk for PsychosisR01MH094650 · NIMH · UNIVERSITY OF COLORADO · PI MITTAL, VIJAY A · 2011 to 2015
$2.3M
Organization and timecourse of the neural mechanisms for cognitive flexibilityF32DA034412 · NIDA · UNIVERSITY OF COLORADO · PI ORR, JOSEPH M. · 2013 to 2015
$122k
Social Processes in individuals at clinical high-risk for psychosisF31MH100821 · NIMH · UNIVERSITY OF COLORADO · PI BALDELLI, ANDREA PELLETIER · 2013 to 2016
$102k
Cerebellar Contributions to Disease Course in Youth At High-Risk of PsychosisF32MH102898 · NIMH · UNIVERSITY OF COLORADO · PI BERNARD, JESSICA ANN · 2013 to 2014
$95k
NIDA NIH HHS F32 DA034412NIMH NIH HHS F31 MH100821NIMH NIH HHS F32 MH102898NIMH NIH HHS R01 MH094650
6 · The paper itself

Abstract

backgroundThe ability to flexibly apply rules to novel situations is a critical aspect of adaptive human behavior. While executive function deficits are known to appear early in the course of psychosis, it is unclear which specific facets are affected. Identifying whether rule learning is impacted at the early stages of psychosis is necessary for truly understanding the etiology of psychosis and may be critical for designing novel treatments. Therefore, we examined rule learning in healthy adolescents and those meeting criteria for clinical high risk (CHR) for psychosis.

methods24 control and 22 CHR adolescents underwent rapid, high-resolution fMRI while performing a paradigm which required them to apply novel or practiced task rules.

resultsPrevious work has suggested that practiced rules rely on rostrolateral prefrontal cortex (RLPFC) during rule encoding and dorsolateral prefrontal cortex (DLPFC) during task performance, while novel rules show the opposite pattern. We failed to replicate this finding, with greater activity for novel rules during performance. Comparing the HC and CHR group, there were no statistically significant effects, but an effect size analysis found that the CHR group showed less activation during encoding and greater activation during performance. This suggests the CHR group may use less efficient reactive control to retrieve task rules at the time of task performance, rather than proactively during rule encoding.

conclusionsThese findings suggest that flexibility is qualitatively altered in the clinical high risk state, however, more data is needed to determine whether these deficits predict disease progression.

Indexed as

AdolescentBrainBrain MappingExecutive FunctionFemaleHumansLearningMagnetic Resonance ImagingMalePrefrontal CortexPsychotic DisordersRiskExecutive functionfMRIHigh riskImagingPsychosisRule learning

Identifiers

PMID32512402
PMCPMC7281799
OpenAlexW3031924390

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.