The association between clinical, sociodemographic, familial, and environmental factors and treatment resistance in schizophrenia: A machine-learning-based approach

被引:1
作者
Van Hooijdonk, Carmen F. M. [1 ,2 ,9 ]
van der Pluijm, Marieke [3 ,4 ]
de Vries, Bart M. [3 ]
Cysouw, Matthijs [3 ]
Alizadeh, Behrooz Z. [5 ,6 ]
Simons, Claudia J. P. [1 ,7 ]
van Amelsvoort, Therese A. M. J. [1 ]
Booij, Jan [3 ]
Selten, Jean-Paul [1 ,2 ]
de Haan, Lieuwe [4 ]
Schirmbeck, Frederike [4 ]
van de Giessen, Elsmarieke [3 ,8 ]
机构
[1] Maastricht Univ, Sch Mental Hlth & Neurosci MHeNS, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[2] Inst Mental Hlth Care, Rivierduinen, Leiden, Netherlands
[3] Univ Amsterdam, Dept Radiol & Nucl Med, Amsterdam UMC, Amsterdam, Netherlands
[4] Univ Amsterdam, Dept Psychiat, Amsterdam UMC, Amsterdam, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Univ Ctr Psychiat, Rob Giel Res Ctr, Groningen, Netherlands
[6] Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[7] GGzE Inst Mental Hlth Care, Eindhoven, Netherlands
[8] Amsterdam Neurosci, Brain Imaging, Amsterdam, Netherlands
[9] Inst Mental Hlth Care, Rivierduinen, POB 405, NL-2300 AK Leiden, Netherlands
关键词
Psychotic disorders; Treatment response; Clozapine; Prediction; Precision medicine; FUNCTIONAL CONNECTIVITY; CLOZAPINE TREATMENT; TREATMENT RESPONSE; 1ST EPISODE; PSYCHOSIS; PREDICTORS; REMISSION; BIOMARKERS; ONSET; BIRTH;
D O I
10.1016/j.schres.2023.10.030
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Prediction of treatment resistance in schizophrenia (TRS) would be helpful to reduce the duration of ineffective treatment and avoid delays in clozapine initiation. We applied machine learning to identify clinical, sociodemographic, familial, and environmental variables that are associated with TRS and could potentially predict TRS in the future.Study design: Baseline and follow-up data on trait(-like) variables from the Genetic Risk and Outcome of Psychosis (GROUP) study were used. For the main analysis, we selected patients with non-affective psychotic disorders who met TRS (n = 200) or antipsychotic-responsive criteria (n = 423) throughout the study. For a sensitivity analysis, we only selected patients who met TRS (n = 76) or antipsychotic-responsive criteria (n = 123) at followup but not at baseline. Random forest models were trained to predict TRS in both datasets. SHapley Additive exPlanation values were used to examine the variables' contributions to the prediction.Study results: Premorbid functioning, age at onset, and educational degree were most consistently associated with TRS across both analyses. Marital status, current household, intelligence quotient, number of moves, and family loading score for substance abuse also consistently contributed to the prediction of TRS in the main or sensitivity analysis. The diagnostic performance of our models was modest (area under the curve: 0.66-0.69).Conclusions: We demonstrate that various clinical, sociodemographic, familial, and environmental variables are associated with TRS. Our models only showed modest performance in predicting TRS. Prospective large multi centre studies are needed to validate our findings and investigate whether the model's performance can be improved by adding data from different modalities.
引用
收藏
页码:132 / 141
页数:10
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