Evidence map›Paper›PMID 35144716›Full record

ArticlePsychological medicine2023

Characterizing sustained social anxiety in individuals at clinical high risk for psychosis: trajectory, risk factors, and functional outcomes.

Wisteria Deng, Jean Addington, Carrie E Bearden, Kristin S Cadenhead, Barbara A Cornblatt, Daniel H Mathalon, Diana O Perkins, Larry J Seidman, Ming T Tsuang, Scott W Woods and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Psychological medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

12 authors at 8 institutions in 2 countries.

Wisteria DengDepartment of Psychology, Yale University, New Haven, CT, USA.ORCID https://orcid.org/0000-0001-6563-7772
Jean AddingtonDepartment of Psychiatry, Hotchkiss Brain Institute, Calgary, Canada.
Carrie E BeardenDepartment of Psychiatry and Biobehavioral Sciences and Psychology, UCLA, Los Angeles, USA.
Kristin S CadenheadDepartment of Psychiatry, UCSD, San Diego, USA.
Barbara A CornblattDepartment of Psychiatry, Zucker Hillside Hospital, Queens, USA.
Daniel H MathalonDepartment of Psychiatry, UCSF, SFVA Medical Center, San Francisco, USA.
Diana O PerkinsDepartment of Psychiatry, University of North Carolina, Chapel Hill, USA.
Larry J SeidmanDepartment of Psychiatry, Harvard Medical School, Boston, USA.
Ming T TsuangDepartment of Psychiatry, UCSD, San Diego, USA.
Scott W WoodsDepartment of Psychiatry, Yale University, New Haven, CT, USA.
Elaine F WalkerDepartment of Psychology and Psychiatry, Emory University, Atlanta, USA.
Tyrone D CannonDepartment of Psychology, Yale University, New Haven, CT, USA.
Yale University · USUniversity of California San Diego · USEmory University · USHarvard University · USNeurobehavioral Systems · USOntario Brain Institute · CAUniversity of North Carolina at Chapel Hill · USZucker Hillside Hospital · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
5/9 Predictors and Mechanisms of Conversion to PsychosisU01MH082004 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PERKINS, DIANA O. · 2008 to 2018
$7.5M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

backgroundWhile comorbidity of clinical high-risk for psychosis (CHR-P) status and social anxiety is well-established, it remains unclear how social anxiety and positive symptoms covary over time in this population. The present study aimed to determine whether there are more than one covariant trajectory of social anxiety and positive symptoms in the North American Prodrome Longitudinal Study cohort (NAPLS 2) and, if so, to test whether the different trajectory subgroups differ in terms of genetic and environmental risk factors for psychotic disorders and general functional outcome.

methodsIn total, 764 CHR individuals were evaluated at baseline for social anxiety and psychosis risk symptom severity and followed up every 6 months for 2 years. Application of group-based multi-trajectory modeling discerned three subgroups based on the covariant trajectories of social anxiety and positive symptoms over 2 years.

resultsOne of the subgroups showed sustained social anxiety over time despite moderate recovery in positive symptoms, while the other two showed recovery of social anxiety below clinically significant thresholds, along with modest to moderate recovery in positive symptom severity. The trajectory group with sustained social anxiety had poorer long-term global functional outcomes than the other trajectory groups. In addition, compared with the other two trajectory groups, membership in the group with sustained social anxiety was predicted by higher levels of polygenic risk for schizophrenia and environmental stress exposures.

conclusionsTogether, these analyses indicate differential relevance of sustained

Indexed as

Psychotic DisordersSchizophreniaAnxietyHumansLongitudinal StudiesProdromal SymptomsRisk FactorsComorbiditycovariant trajectoriesoutcome studiespolygenic riskstress exposure

Identifiers

PMID35144716
PMCPMC10277760
OpenAlexW4210997590

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LicenceCC BY
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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.