Evidence map›Paper›PMID 24080895›Full record

ArticleSchizophrenia bulletin2014

Elevated antisaccade error rate as an intermediate phenotype for psychosis across diagnostic categories.

James L Reilly, Kyle Frankovich, Scot Hill, Elliot S Gershon, Richard S E Keefe, Matcheri S Keshavan, Godfrey D Pearlson, Carol A Tamminga, John A Sweeney

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–field-weighted citation impact
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

51 citing papers in PubMed.

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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

9 authors.

James L ReillyDepartment of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL; james.reilly@northwestern.edu.
Kyle FrankovichCenter for Mind and Brain and Department of Psychology, University of California at Davis, Davis, CA;
Scot HillDepartment of Psychology, Rosalind Franklin University of Medicine and Science, Chicago, IL;
Elliot S GershonDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL;
Richard S E KeefeDepartment of Psychiatry, Duke University, Durham, NC;
Matcheri S KeshavanBeth Israel Deaconess Hospital and Massachusetts Mental Health Center, Harvard Medical School, Boston, MA;
Godfrey D PearlsonOlin Neuropsychiatry Research Center, Yale School of Medicine, New Haven, CT; Department of Psychiatry, Institute of Living/Hartford Hospital, Hartford, CT;
Carol A TammingaDepartment of Psychiatry, UT Southwestern Medical School, Dallas, TX.
John A SweeneyDepartment of Psychiatry, UT Southwestern Medical School, Dallas, TX.

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Bipolar & Schizophrenia Consortium for Parsing Intermediate PhenotypesR01MH077851 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2007 to 2019
$7.8M
Bipolar & Schizophrenia Consortium for Parsing Intermediate PhenotypesR01MH077945 · NIMH · YALE UNIVERSITY · PI PEARLSON, GODFREY D · 2007 to 2019
$7.6M
Stability of Biotypes: a Longitudinal EvaluationR01MH078113 · NIMH · WAYNE STATE UNIVERSITY · PI KESHAVAN, MATCHERI S. · 2007 to 2019
$6.2M
Stability of Biotypes: a Longitudinal Evaluation (STABLE)R01MH103368 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S, KEEDY, SARAH K · 2015 to 2019
$4.5M
Bipolar & Schizophrenia Consortium for Parsing Intermediate PhenotypesR01MH077852 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI THAKER, GUNVANT K · 2007 to 2010
$3.5M
Bipolar & Schizophrenia Consortium for Parsing Intermediate PhenotypesR01MH077862 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI SWEENEY, JOHN A · 2007 to 2010
$3.1M
Psychosis and Affective Research Domains and Intermediate Phenotypes (PARDIP)R01MH096913 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2013 to 2015
$950k
Antipsychotic Treatment Effects on Attention & Working Memory in SchizophreniaK23MH083126 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REILLY, JAMES L · 2009 to 2013
$819k
NCATS NIH HHS UL1 TR000430NIMH NIH HHS MH077851NIMH NIH HHS MH077852NIMH NIH HHS MH077862NIMH NIH HHS MH077945NIMH NIH HHS MH078113NIMH NIH HHS MH083126NIMH NIH HHS R01 MH096913NIMH NIH HHS R01 MH103368
6 · The paper itself

Abstract

backgroundElevated antisaccade error rate, reflecting problems with inhibitory behavioral control, is a promising intermediate phenotype for schizophrenia. Here, we consider whether it marks liability across psychotic disorders via common or different neurophysiological mechanisms and whether it represents a neurocognitive risk indicator apart from the generalized cognitive deficit.

methodsSchizophrenia (n = 267), schizoaffective (n = 150), and psychotic bipolar (n = 202) probands, their first-degree relatives (ns = 304, 193, 242, respectively), and healthy controls (n = 244), participating in the Bipolar-Schizophrenia Network on Intermediate Phenotypes consortium, performed antisaccade and prosaccade tasks and completed a neuropsychological battery.

resultsAntisaccade error rate was elevated in proband groups with greatest deficit observed in schizophrenia and was unrelated to symptoms and antipsychotic treatment. Increased error rate was also observed among relatives, even those without history of psychosis or psychosis spectrum personality traits. Relatives' deficits were similar across proband diagnoses. Error rate was familial and remained elevated in proband and relative groups after accounting for generalized cognitive impairment. Speed of attentional shifting, indexed by prosaccade latency, was similarly influenced in all groups by manipulations that freed vs increasingly engaged attention systems and was inversely associated with antisaccade error rate in all but schizophrenia probands.

conclusionsThese findings indicate that elevated antisaccade error rate represents an intermediate phenotype for psychosis across diagnostic categories, and that it tracks risk beyond that attributable to the generalized cognitive deficit. The greater severity of antisaccade impairment in schizophrenia and its independence from attention shifting processes suggest more severe and specific prefrontal inhibitory control deficits in this disorder.

Indexed as

EndophenotypesAdultBipolar DisorderExecutive FunctionFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedNuclear FamilyPsychomotor PerformancePsychotic DisordersSaccadesSchizophreniabipolar disorderendophenotypefamily studyschizoaffective disorderschizophrenia

Identifiers

PMID24080895
PMCPMC4133662

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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.