TY - JOUR
T1 - Development and Validation of Predictive Model for a Diagnosis of First Episode Psychosis Using the Multinational EU-GEI Case-control Study and Modern Statistical Learning Methods
AU - Ajnakina, Olesya
AU - Fadilah, Ihsan
AU - Quattrone, Diego
AU - Arango, Celso
AU - Berardi, Domenico
AU - Bernardo, Miguel
AU - Bobes, Julio
AU - De Haan, Lieuwe
AU - Del-Ben, Cristina Marta
AU - Gayer-Anderson, Charlotte
AU - Stilo, Simona
AU - Jongsma, Hannah E.
AU - Lasalvia, Antonio
AU - Tosato, Sarah
AU - Llorca, Pierre Michel
AU - Menezes, Paulo Rossi
AU - Rutten, Bart P.
AU - Santos, Jose Luis
AU - Sanjuán, Julio
AU - Selten, Jean Paul
AU - Szöke, Andrei
AU - Tarricone, Ilaria
AU - D'Andrea, Giuseppe
AU - Tortelli, Andrea
AU - Velthorst, Eva
AU - Jones, Peter B.
AU - Romero, Manuel Arrojo
AU - La Cascia, Caterina
AU - Kirkbride, James B.
AU - Van Os, Jim
AU - O'Donovan, Michael
AU - Morgan, Craig
AU - Di Forti, Marta
AU - Murray, Robin M.
AU - Hubbard, Kathryn
AU - Stahl, Daniel
N1 - Funding Information:
OA is funded by the National Institute for Health Research (NIHR) (NIHR Post-Doctoral Fellowship—PDF-2018-11-ST2-020). IF is funded by NIHR Predoctoral Fellowship (NIHR300493). MDF is funded by Clinician Scientist Medical Research Council fellowship (project reference MR/M008436/1). DQ is funded by Post-Doctoral Guarantors of Brain Clinical Fellowship. DS is funded part funded by the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. JBK is supported by National Institute for Health Research, University College London Hospital, Biomedical Research Centre. The EU-GEI Project is funded by the European Community’s Seventh Framework Programme under grant agreement No. HEALTH-F2-2010-241909 (Project EU-GEI). The Brazilian study was funded by the São Paulo Research Foundation under grant number 2012/0417-0. The views expressed in this publication are those of the authors and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health and Social Care.
Publisher Copyright:
© 2023 The Author(s). Published by Oxford University Press on behalf of the University of Maryland's school of medicine, Maryland Psychiatric Research Center.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background and Hypothesis: It is argued that availability of diagnostic models will facilitate a more rapid identification of individuals who are at a higher risk of first episode psychosis (FEP). Therefore, we developed, evaluated, and validated a diagnostic risk estimation model to classify individual with FEP and controls across six countries. Study Design: We used data from a large multi-center study encompassing 2627 phenotypically well-defined participants (aged 18-64 years) recruited from six countries spanning 17 research sites, as part of the European Network of National Schizophrenia Networks Studying Gene-Environment Interactions study. To build the diagnostic model and identify which of important factors for estimating an individual risk of FEP, we applied a binary logistic model with regularization by the least absolute shrinkage and selection operator. The model was validated employing the internal-external cross-validation approach. The model performance was assessed with the area under the receiver operating characteristic curve (AUROC), calibration, sensitivity, and specificity. Study Results: Having included preselected 22 predictor variables, the model was able to discriminate adults with FEP and controls with high accuracy across all six countries (rangesAUROC=0.84-0.86). Specificity (range=73.9-78.0%) and sensitivity (range=75.6-79.3%) were equally good, cumulatively indicating an excellent model accuracy; though, calibration slope for the diagnostic model showed a presence of some overfitting when applied specifically to participants from France, the UK, and The Netherlands. Conclusions: The new FEP model achieved a good discrimination and good calibration across six countries with different ethnic contributions supporting its robustness and good generalizability.
AB - Background and Hypothesis: It is argued that availability of diagnostic models will facilitate a more rapid identification of individuals who are at a higher risk of first episode psychosis (FEP). Therefore, we developed, evaluated, and validated a diagnostic risk estimation model to classify individual with FEP and controls across six countries. Study Design: We used data from a large multi-center study encompassing 2627 phenotypically well-defined participants (aged 18-64 years) recruited from six countries spanning 17 research sites, as part of the European Network of National Schizophrenia Networks Studying Gene-Environment Interactions study. To build the diagnostic model and identify which of important factors for estimating an individual risk of FEP, we applied a binary logistic model with regularization by the least absolute shrinkage and selection operator. The model was validated employing the internal-external cross-validation approach. The model performance was assessed with the area under the receiver operating characteristic curve (AUROC), calibration, sensitivity, and specificity. Study Results: Having included preselected 22 predictor variables, the model was able to discriminate adults with FEP and controls with high accuracy across all six countries (rangesAUROC=0.84-0.86). Specificity (range=73.9-78.0%) and sensitivity (range=75.6-79.3%) were equally good, cumulatively indicating an excellent model accuracy; though, calibration slope for the diagnostic model showed a presence of some overfitting when applied specifically to participants from France, the UK, and The Netherlands. Conclusions: The new FEP model achieved a good discrimination and good calibration across six countries with different ethnic contributions supporting its robustness and good generalizability.
KW - cannabis use
KW - diagnostic prediction modeling/risk prediction
KW - psychosis/diagnostic factors
UR - http://www.scopus.com/inward/record.url?scp=85172381864&partnerID=8YFLogxK
U2 - 10.1093/schizbullopen/sgad008
DO - 10.1093/schizbullopen/sgad008
M3 - Article
AN - SCOPUS:85172381864
SN - 2632-7899
VL - 4
JO - Schizophrenia Bulletin Open
JF - Schizophrenia Bulletin Open
IS - 1
M1 - sgad008
ER -