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Improving Prognostic Accuracy in Subjects at Clinical High Risk for Psychosis: Systematic Review of Predictive Models and Meta-analytical Sequential Testing Simulation
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3720849
Author(s) Schmidt, André; Cappucciati, Marco; Radua, Joaquim; Rutigliano, Grazia; Rocchetti, Matteo; Dell'Osso, Liliana; Politi, Pierluigi; Borgwardt, Stefan; Reilly, Thomas; Valmaggia, Lucia; McGuire, Philip; Fusar-Poli, Paolo
Author(s) at UniBasel Schmidt, André
Year 2016
Title Improving Prognostic Accuracy in Subjects at Clinical High Risk for Psychosis: Systematic Review of Predictive Models and Meta-analytical Sequential Testing Simulation
Journal Schizophrenia bulletin
Volume 43
Number 2
Pages / Article-Number 375-388
Mesh terms Humans; Models, Theoretical; Prognosis; Psychotic Disorders, physiopathology
Abstract Discriminating subjects at clinical high risk (CHR) for psychosis who will develop psychosis from those who will not is a prerequisite for preventive treatments. However, it is not yet possible to make any personalized prediction of psychosis onset relying only on the initial clinical baseline assessment. Here, we first present a systematic review of prognostic accuracy parameters of predictive modeling studies using clinical, biological, neurocognitive, environmental, and combinations of predictors. In a second step, we performed statistical simulations to test different probabilistic sequential 3-stage testing strategies aimed at improving prognostic accuracy on top of the clinical baseline assessment. The systematic review revealed that the best environmental predictive model yielded a modest positive predictive value (PPV) (63%). Conversely, the best predictive models in other domains (clinical, biological, neurocognitive, and combined models) yielded PPVs of above 82%. Using only data from validated models, 3-stage simulations showed that the highest PPV was achieved by sequentially using a combined (clinical + electroencephalography), then structural magnetic resonance imaging and then a blood markers model. Specifically, PPV was estimated to be 98% (number needed to treat, NNT = 2) for an individual with 3 positive sequential tests, 71%-82% (NNT = 3) with 2 positive tests, 12%-21% (NNT = 11-18) with 1 positive test, and 1% (NNT = 219) for an individual with no positive tests. This work suggests that sequentially testing CHR subjects with predictive models across multiple domains may substantially improve psychosis prediction following the initial CHR assessment. Multistage sequential testing may allow individual risk stratification of CHR individuals and optimize the prediction of psychosis.
Publisher Oxford University Press
ISSN/ISBN 0586-7614 ; 1745-1701
URL https://academic.oup.com/schizophreniabulletin/article/43/2/375/2503511
edoc-URL https://edoc.unibas.ch/63108/
Full Text on edoc Available
Digital Object Identifier DOI 10.1093/schbul/sbw098
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/27535081
ISI-Number WOS:000396511600006
Document type (ISI) Journal Article, Review
 
   

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