{"title":"Machine Learning-Based Discrimination of Treatment-Resistant Schizophrenia Using Structural Brain Imaging: A Multi-Site Proof-of-Concept Study.","authors":"Edgardo Torres-Carmona, Mario Graff-Guerrero, Shinichiro Nakajima, Yusuke Iwata, Fumihiko Ueno, Teruki Koizumi, Shiori Honda, Sakiko Tsugawa, Saki Homma, Kamiyu Ogyu, Ryosuke Tarumi, Jianmeng Song, Vincenzo Deluca, Gary Remington, Philip Gerretsen, Ariel Graff-Guerrero","doi":"10.1016/j.biopsych.2026.08.009","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Treatment-resistant schizophrenia (TRS) affects 20-30% of individuals with schizophrenia, with persistent symptoms, functional impairment, and reduced quality of life. Clinical identification remains dependent on sequential antipsychotic trials despite reported structural brain differences between TRS and treatment-responsive schizophrenia (TxR). This study evaluated whether structural MRI features could discriminate clinically defined TRS from TxR using machine learning.</p><p><strong>Methods: </strong>A total of 225 participants (122 TRS, 103 TxR) from multi-site studies in Canada and Japan were included. Cortical thickness, brain volume, surface area, and intrinsic curvature were derived from T1-weighted MRI using FreeSurfer, with feature engineering generating volumetric-cortical thickness interaction terms. A voting ensemble was evaluated under a primary leakage-controlled NeuroComBat harmonization and a secondary exploratory full-dataset harmonization. Performance was assessed using ROC-AUC, F1 score, precision, and recall.</p><p><strong>Results: </strong>In the leakage-controlled analysis, the voting ensemble achieved a held-out ROC-AUC of 0.57 and macro F1 of 0.56; training cross-validation yielded ROC-AUC of 0.715. The full-dataset harmonization analysis yielded ROC-AUC of 0.60 and macro F1 of 0.62, interpreted cautiously due to leakage. Temporal-occipital cortical thickness and choroid plexus volume interaction terms contributed most to model performance.</p><p><strong>Conclusion: </strong>Structural MRI features may support cross-sectional discrimination of TRS from TxR. The divergence between harmonization strategies highlights the importance of leakage-aware preprocessing in neuroimaging. Validation in independent cohorts is required to establish whether these features contribute to earlier identification of treatment resistance.</p>","PeriodicalId":8918,"journal":{"name":"Biological Psychiatry","volume":" ","pages":""},"PeriodicalIF":10.3000,"publicationDate":"2026-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.biopsych.2026.08.009","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Treatment-resistant schizophrenia (TRS) affects 20-30% of individuals with schizophrenia, with persistent symptoms, functional impairment, and reduced quality of life. Clinical identification remains dependent on sequential antipsychotic trials despite reported structural brain differences between TRS and treatment-responsive schizophrenia (TxR). This study evaluated whether structural MRI features could discriminate clinically defined TRS from TxR using machine learning.
Methods: A total of 225 participants (122 TRS, 103 TxR) from multi-site studies in Canada and Japan were included. Cortical thickness, brain volume, surface area, and intrinsic curvature were derived from T1-weighted MRI using FreeSurfer, with feature engineering generating volumetric-cortical thickness interaction terms. A voting ensemble was evaluated under a primary leakage-controlled NeuroComBat harmonization and a secondary exploratory full-dataset harmonization. Performance was assessed using ROC-AUC, F1 score, precision, and recall.
Results: In the leakage-controlled analysis, the voting ensemble achieved a held-out ROC-AUC of 0.57 and macro F1 of 0.56; training cross-validation yielded ROC-AUC of 0.715. The full-dataset harmonization analysis yielded ROC-AUC of 0.60 and macro F1 of 0.62, interpreted cautiously due to leakage. Temporal-occipital cortical thickness and choroid plexus volume interaction terms contributed most to model performance.
Conclusion: Structural MRI features may support cross-sectional discrimination of TRS from TxR. The divergence between harmonization strategies highlights the importance of leakage-aware preprocessing in neuroimaging. Validation in independent cohorts is required to establish whether these features contribute to earlier identification of treatment resistance.
期刊介绍:
Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.