TY - JOUR
T1 - Prediction of relapse in a French cohort of outpatients with schizophrenia (FACE-SZ)
T2 - Prediction, not association
AU - Barbosa, Susana
AU - Tamouza, Ryad
AU - Leboyer, Marion
AU - Aouizerate, Bruno
AU - Andrieu, Christelle
AU - Andre, Myrtille
AU - Boukouaci, Wahid
AU - Capdevielle, Delphine
AU - Chereau, Isabelle
AU - Kobayashi, Julie Clauss
AU - Coulon, Nathalie
AU - Dorey, Jean-Michel
AU - Davidovic, Laetitia
AU - Dubertret, Caroline
AU - Fakra, Eric
AU - Fond, Guillaume
AU - Goze, Tudi
AU - Khalfallah, Olfa
AU - Leignier, Sylvain
AU - Llorca, Pierre Michel
AU - Mallet, Jasmina
AU - Martinuzzi, Emanuela
AU - Misdrahi, David
AU - Oriol, Nicolas
AU - Pignon, Baptiste
AU - Rey, Romain
AU - Roux, Paul
AU - Schürhoff, Franck
AU - Schorr, Benoit
AU - Urbach, Mathieu
AU - Very, Etienne
AU - Wu, Ching-Lien
AU - Benros, Michael
AU - Simon, Judit
AU - Hasan, Alkomiet
AU - Glaichenhaus, Nicolas
AU - Godin, Ophélia
AU - FondaMental Academic Centers of Expertise for Schizophrenia (FACE-SZ) collaborators
N1 - Copyright © 2024. Published by Elsevier Inc.
PY - 2025/3/20
Y1 - 2025/3/20
N2 - BACKGROUND: Schizophrenia (SZ) commonly manifests through multiple relapses, each impeding the path to recovery and incurring personal and societal costs. Despite the identification of various risk factors associated to the risk of relapse, the development of accurate algorithms predictive of relapse has been limited, partly due to inadequate statistical methods. Additionally, despite the wealth of data showing strong associations between inflammation and schizophrenia, the two existing studies failed to demonstrate whether inflammatory parameters could predict relapse. Our goal is then to identify clinical and inflammatory parameters associated with relapse in schizophrenia and to develop model to predict relapse in each patient.METHODS: We have used classical Cox regression, survival penalized regression, as well as survival random forests to analyze clinical and inflammatory biological data collected in the network of the Schizophrenia Expert Centers in France in which individuals with SZ are clinically assessed and followed up annually for 3 years.RESULTS: Among 247 individuals with SZ, 71 (29 %) experienced a psychotic relapse during the 3-year follow-up period. The variables most consistently associated with relapses were smoking status, severity of positive symptoms and low global functioning. From a panel of inflammatory parameters, only IL-8 serum levels were associated with time to relapse. The predictive performance, assessed using C-index, was 0.54 using both penalized regression and random forests.CONCLUSIONS: We found several clinical and biological variables consistently associated with relapses across three distinct statistical methods. However, despite these associations, the predictive capacity of these models remained low, highlighting that association does not necessarily mean prediction.
AB - BACKGROUND: Schizophrenia (SZ) commonly manifests through multiple relapses, each impeding the path to recovery and incurring personal and societal costs. Despite the identification of various risk factors associated to the risk of relapse, the development of accurate algorithms predictive of relapse has been limited, partly due to inadequate statistical methods. Additionally, despite the wealth of data showing strong associations between inflammation and schizophrenia, the two existing studies failed to demonstrate whether inflammatory parameters could predict relapse. Our goal is then to identify clinical and inflammatory parameters associated with relapse in schizophrenia and to develop model to predict relapse in each patient.METHODS: We have used classical Cox regression, survival penalized regression, as well as survival random forests to analyze clinical and inflammatory biological data collected in the network of the Schizophrenia Expert Centers in France in which individuals with SZ are clinically assessed and followed up annually for 3 years.RESULTS: Among 247 individuals with SZ, 71 (29 %) experienced a psychotic relapse during the 3-year follow-up period. The variables most consistently associated with relapses were smoking status, severity of positive symptoms and low global functioning. From a panel of inflammatory parameters, only IL-8 serum levels were associated with time to relapse. The predictive performance, assessed using C-index, was 0.54 using both penalized regression and random forests.CONCLUSIONS: We found several clinical and biological variables consistently associated with relapses across three distinct statistical methods. However, despite these associations, the predictive capacity of these models remained low, highlighting that association does not necessarily mean prediction.
KW - Immune system
KW - Inflammation
KW - Machine learning
KW - Prediction
KW - Relapse
KW - Schizophrenia
KW - Word count = 3637.
UR - https://www.scopus.com/pages/publications/85219060103
U2 - 10.1016/j.pnpbp.2025.111304
DO - 10.1016/j.pnpbp.2025.111304
M3 - Journal article
C2 - 40023308
SN - 0278-5846
VL - 137
JO - Progress in neuro-psychopharmacology & biological psychiatry
JF - Progress in neuro-psychopharmacology & biological psychiatry
M1 - 111304
ER -