Evidence map›Paper›PMID 35144059›Full record

ArticleSchizophrenia research2022

Longitudinal and cross-sectional validation of the WERCAP screen for assessing psychosis risk and conversion.

Daniel Mamah, Victoria N Mutiso, David M Ndetei

Abstract read
In one paragraph

Article in Schizophrenia research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  4. Real-world comprehensive care of people living with schizophrenia: recommendations across different settings and clinical stages.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2026
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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

3 authors.

Daniel MamahDepartment of Psychiatry, Washington University Medical School, St. Louis, MO, United States of America. Electronic address: mamahd@wustl.edu.
Victoria N MutisoAfrica Mental Health Research and Training Foundation, Nairobi, Kenya.
David M NdeteiAfrica Mental Health Research and Training Foundation, Nairobi, Kenya; Department of Psychiatry, University of Nairobi, Kenya.

Funding

ProNET: Psychosis-Risk Outcomes NetworkU01MH124639 · NIMH · YALE UNIVERSITY · PI CARRIE E BEARDEN, JOHN M KANE · 2020 to 2026
$81.2M
Clinical and Biomarker-Based Trajectories of Psychosis-Risk Populations in KenyaR01MH127571 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2021 to 2025
$3.3M
Neurodevelopment and Psychosis in the 22q11.2 Copy Number VariantsR37MH085953 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CARRIE E BEARDEN · 2023 to 2026
$2.9M
Genes, Behavior and Psychosis Risk in KenyaR56MH111300 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2016 to 2016
$640k
Identifying Imaging Biomarkers of Schizophrenia-Risk in KenyaR21MH124060 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2020 to 2020
$334k
IDENTIFICATION OF PSYCHOSIS-RISK TRAITS IN AFRICAR21MH095645 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL · 2013 to 2014
$270k
NIMH NIH HHS R01 MH127571NIMH NIH HHS R21 MH095645NIMH NIH HHS R21 MH124060NIMH NIH HHS R37 MH085953NIMH NIH HHS R56 MH111300NIMH NIH HHS U01 MH124639
6 · The paper itself

Abstract

backgroundThe Washington Early Recognition Center Affectivity and Psychosis (WERCAP) Screen was developed to assess risk for developing psychosis. Its validity has not been investigated in a large population-based study or with longitudinal analyses.

methods825 participants, aged 14-25, were recruited from Kenya. Symptoms were assessed using the WERCAP Screen, as experienced over the prior 3-months (3MO), 12-months (12MO) or lifetime (LIF). ROC curve analysis was used to determine the validity of the WERCAP Screen against the Structured Interview of Psychosis-Risk Syndromes. Longitudinal validity was assessed by comparing baseline p-WERCAP scores in psychotic disorder converters and non-converters, and using ROC curve analysis. Relationship of the p-WERCAP was examined against clinical variables.

resultsROC curve analyses against SIPS showed an AUC of 0.83 for 3MO, 0.79 for 12MO and 0.65 for LIF psychosis scores. The optimal cut-point on 3MO was a score of >12 (sens: 0.78; spec: 0.77; ppv: 0.41), and >32 for 12MO (sens: 0.71; spec: 0.74; ppv: 0.24). Baseline 3MO scores (but not LIF scores) were higher in converters compared to high-risk non-converters (p = 0.02). 3MO scores against conversion status had an AUC of 0.75, with an optimal cutoff point of >16 (sens: 1.0; spec: 0.53). All p-WERCAP scores significantly correlated with substance use and stress severity. 12 MO scores were most related to cognitive impairment.

conclusionsThe WERCAP Screen is a valid instrument for assessing psychosis severity and conversion risk. It can be used in the community to identify those who may require clinical assessment and care, and for recruitment in psychosis-risk research.

Indexed as

Psychotic DisordersAdolescentAdultCross-Sectional StudiesHumansProdromal SymptomsRecognition, PsychologyROC CurveWashingtonYoung AdultKenyaPsychosisRiskStress screenValidationWERCAP

Identifiers

PMID35144059
PMCPMC10448956

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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.