Evidence map›Paper›PMID 32201031›Full record

ArticleSchizophrenia research2020

Clarifying the direction of impact of negative symptoms and neurocognition on prospective work functioning in psychosis: A 20-year longitudinal study.

Lauren Luther, Jennifer H Suor, Cherise Rosen, Thomas H Jobe, Robert N Faull, Martin Harrow

Abstract read
In one paragraph

Article in Schizophrenia research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  11. Activation of Internal Correctness Monitoring Circuitry in Youths With Psychosis Spectrum Symptoms.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2023
    Article
  12. Mediators of quality of life change in people with severe psychotic disorders treated in integrated care: ACCESS II study.European psychiatry : the journal of the Association of European Psychiatrists · 2022
    Article
  13. Article
  14. Frontiers in psychiatry · 2022
    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.

Lauren LutherMassachusetts General Hospital, Department of Psychiatry, 149 13th Street, Charlestown, MA 02129, USA; Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA; University of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: lluther1@mgh.harvard.edu.
Jennifer H SuorUniversity of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: jesuor@uic.edu.
Cherise RosenUniversity of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: ccrosen@uic.edu.
Thomas H JobeUniversity of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: thjobe@gmail.com.
Robert N FaullUniversity of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: rfaul@uic.edu.
Martin HarrowUniversity of Illinois at Chicago, Department of Psychiatry, 1601 West Taylor, Chicago, IL 60612, USA. Electronic address: mharrow@uic.edu.

Funding

Stuart T. Hauser Research Training Program in Biological and Social Psychiatry.T32MH016259 · NIMH · JUDGE BAKER CHILDREN'S CENTER · PI Marek Kubicki, Martha E. Shenton · 1985 to 2026
$8.4M
Predicting and Preventing High-Risk Adolescent Behavior F32HD100075 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUOR, JENNIFER · 2019 to 2022
$205k
NICHD NIH HHS F32 HD100075NIMH NIH HHS T32 MH016259
6 · The paper itself

Abstract

Both neurocognition and negative symptoms have demonstrated strong links to functional outcomes, such as work functioning, among those with severe mental illness (SMI). Prior models have suggested that reduced neurocognition 1) precedes or predicts greater negative symptoms and 2) indirectly influences functional outcomes via its impact on negative symptoms. The current study sought to also test a divergent model: whether greater negative symptoms predict reduced neurocognition and indirectly influence work functioning through their impact on neurocognition. Both models were tested using cross-sectional and prospective data spanning 20-years in a sample of 277 people with a SMI with psychotic features. Results showed that both models were supported in cross-sectional analyses. However, in prospective models predicting work functioning, only the models examining the indirect influence of negative symptoms on work functioning (7.5 to up to 20-years later) through neurocognition demonstrated significant mediation (i.e., a significant indirect effect); further, higher negative symptoms significantly predicted lower prospective neurocognition, while lower neurocognition did not significantly predict greater prospective negative symptoms. Although cross-sectional data were consistent with prior models, our prospective models offered greater support for a putative causal pathway running from negative symptoms to neurocognition-rather than the reverse-to work functioning. Findings have implications for mechanisms contributing to longitudinal work functioning and suggest that targeting negative symptoms prior to neurocognition could be more beneficial for long-term work outcomes.

Indexed as

Psychotic DisordersCross-Sectional StudiesHumansLongitudinal StudiesNeuropsychological TestsProspective StudiesNegative symptomsNeurocognitionPsychosisSevere mental illnessVocational rehabilitationWork

Identifiers

PMID32201031
PMCPMC8523216

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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.