Models Predicting Psychosis in Patients With High Clinical Risk: A Systematic Review

The present study reviews predictive models used to improve prediction of psychosis onset in individuals at clinical high risk for psychosis (CHR), using clinical, biological, neurocognitive, environmental, and combinations of predictors. A systematic literature search on PubMed was carried out (fro...

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Published inFrontiers in psychiatry Vol. 11; p. 223
Main Authors Montemagni, Cristiana, Bellino, Silvio, Bracale, Nadja, Bozzatello, Paola, Rocca, Paola
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 24.03.2020
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Summary:The present study reviews predictive models used to improve prediction of psychosis onset in individuals at clinical high risk for psychosis (CHR), using clinical, biological, neurocognitive, environmental, and combinations of predictors. A systematic literature search on PubMed was carried out (from 1998 through 2019) to find all studies that developed or validated a model predicting the transition to psychosis in CHR subjects. We found 1,406 records. Thirty-eight of them met the inclusion criteria; 11 studies using clinical predictive models, seven studies using biological models, five studies using neurocognitive models, five studies using environmental models, and 18 studies using combinations of predictive models across different domains. While the highest positive predictive value (PPV) in clinical, biological, neurocognitive, and combined predictive models were relatively high (all above 83), the highest PPV across environmental predictive models was modest (63%). Moreover, none of the combined models showed a superiority when compared with more parsimonious models (using only neurocognitive, clinical, biological, or environmental factors). The use of predictive models may allow high prognostic accuracy for psychosis prediction in CHR individuals. However, only ten studies had performed an internal validation of their models. Among the models with the highest PPVs, only the biological and neurocognitive but not the combined models underwent validation. Further validation of predicted models is needed to ensure external validity.
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Edited by: Alexandre Heeren, Catholic University of Louvain, Belgium
Reviewed by: Maria Semkovska, University of Southern Denmark, Denmark; Grazia Rutigliano, University of Pisa, Italy
This article was submitted to Psychopathology, a section of the journal Frontiers in Psychiatry
ISSN:1664-0640
1664-0640
DOI:10.3389/fpsyt.2020.00223