Evidence map›Paper›PMID 30106252›Full record

Trial reportBrain and behavior2018

Enhanced switching and familial susceptibility for psychosis.

Fred W Sabb, Gerhard Hellemann, Nicholas B Allen, Carrie E Bearden

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Brain and behavior, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Trial
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

4 authors at 3 institutions in 1 country.

Fred W SabbLewis Center for Neuroimaging, University of Oregon, Eugene, Oregon.ORCID 0000-0001-6098-787X
Gerhard HellemannSemel Institute for Neuroscience and Human Behavior, UCLA, Los Angeles, California.
Nicholas B AllenDepartment of Psychology, University of Oregon, Eugene, Oregon.
Carrie E BeardenSemel Institute for Neuroscience and Human Behavior, UCLA, Los Angeles, California.
University of Oregon · USAllen Institute for Brain Science · USCenter for Neurosciences · US

Funding

Translational Research to Enhance Cognitive ControlP50MH077248 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCCRACKEN, JAMES T. · 2006 to 2011
$9.2M
High-Throughput Cognitive Phenomics: A Novel Framework for Psychiatric GWASR01MH091669 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SABB, FRED W. · 2010 to 2012
$841k
NIMH NIH HHS P50 MH077248NIMH NIH HHS R01 MH091669
6 · The paper itself

Abstract

introductionWorking Memory and Task-Switching are essential components of cognitive control, which underlies many symptoms evident across multiple neuropsychiatric disorders, including psychotic and mood disorders. Vulnerability to these disorders has a substantial genetic component, suggesting that clinically unaffected first-degree relatives may carry some vulnerability-related traits. Converging evidence from animal and human studies demonstrates that dopamine transmission, striatal and frontal brain regions, and attention and switching behaviors are essential components of a multilevel circuit involved in salience, and disruptions in that circuit may lead to features of psychosis. Yet, it is possible that unaffected relatives may also possess characteristics that protect against development of illness. We hypothesized that reduced switch cost in a cued task-switching task, may be a behavioral expression of this "resilience" phenotype that will be observable in unaffected relatives.

methodsWe tested a large community sample (n = 536) via the web, to assess different subcomponents of cognitive control, including task-switching and working memory, as well as risk-taking, among individuals who report having an affected relative with a psychotic or mood disorder.

resultsHealthy individuals with suspected genetic risk due to a self-reported familial history of a psychotic disorder demonstrated better task-switching performance compared to healthy people without a psychiatrically ill relative and those with a relative with a mood disorder. This result was specific to illness status and task domain, in that individuals with a personal history of depression or anxiety did not show improved task-switching performance, and this improvement was selective to task-switching and not seen in other putative cognitive control domains (working memory or risk taking).

conclusionsAlthough this study has limitations and independent replication is needed, these preliminary findings suggest a potential avenue for understanding susceptibility to these disorders by highlighting possible protective as well as vulnerability-related aspects of risk phenotypes.

Indexed as

AdultAttentionFemaleFrontal LobeHumansMaleMemory, Short-TermNeuropsychological TestsPhenotypePsychotic DisordersReaction TimeResilience, PsychologicalRisk FactorsSelf ReportSpatial MemoryYoung Adultcognitive controlHeritabilityInternetphenotyperesilienceset shiftingvulnerability

Identifiers

PMID30106252
PMCPMC5991556
OpenAlexW2799930921

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.