Using combined environmental-clinical classification models to predict role functioning outcome in clinical high-risk states for psychosis and recent-onset depression

被引:2
|
作者
Antonucci, Linda A. [1 ,2 ]
Penzel, Nora [2 ,3 ,4 ]
Sanfelici, Rachele [2 ,5 ]
Pigoni, Alessandro [6 ,7 ]
Kambeitz-Ilankovic, Lana [2 ,3 ,4 ]
Dwyer, Dominic [2 ]
Ruef, Anne [2 ]
Sen Dong, Mark [2 ]
Ozturk, Omer Faruk [2 ,8 ]
Chisholm, Katharine [9 ,10 ]
Haidl, Theresa [3 ,4 ]
Rosen, Marlene [3 ,4 ]
Ferro, Adele [6 ]
Pergola, Giulio [11 ]
Andriola, Ileana [11 ]
Blasi, Giuseppe [11 ]
Ruhrmann, Stephan [3 ,4 ]
Schultze-Lutter, Frauke [12 ,13 ,14 ]
Falkai, Peter [2 ]
Kambeitz, Joseph [3 ,4 ]
Lencer, Rebekka [15 ,16 ]
Dannlowski, Udo [15 ]
Upthegrove, Rachel [9 ,17 ]
Salokangas, Raimo K. R. [18 ]
Pantelis, Christos [19 ]
Meisenzahl, Eva [12 ]
Wood, Stephen J. [2 ,20 ,21 ,22 ]
Brambilla, Paolo [6 ,23 ]
Borgwardt, Stefan [15 ,24 ]
Bertolino, Alessandro [11 ]
Koutsouleris, Nikolaos [2 ]
机构
[1] Univ Bari Aldo Moro, Dept Educ Sci Psychol & Commun Sci, Bari, Italy
[2] Ludwig Maximilians Univ Munchen, Dept Psychiat & Psychotherapy, Munich, Germany
[3] Univ Cologne, Dept Psychiat & Psychotherapy, Fac Med, Cologne, Germany
[4] Univ Cologne, Univ Hosp Cologne, Cologne, Germany
[5] Max Planck Sch Cognit, Inst Psychiat, Leipzig, Germany
[6] Fdn IRCCS CaGranda Osped Maggiore Policlin, Dept Neurosci & Mental Hlth, Milan, Italy
[7] IMT Sch Adv Studies Lucca, MoMiLab, Social & Affect Neurosci Grp, Lucca, Italy
[8] Int Max Planck Res Sch Translat Psychiat, Inst Psychiat, Munich, Germany
[9] Univ Birmingham, Inst Mental Hlth, Birmingham, W Midlands, England
[10] Aston Univ, Dept Psychol, Birmingham, W Midlands, England
[11] Univ Bari Aldo Moro, Dept Basic Med Sci Neurosci & Sense Organs, Bari, Italy
[12] Heinrich Heine Univ Dusseldorf, Dept Psychiat & Psychotherapy, Dusseldorf, Germany
[13] Airlangga Univ, Fac Psychol, Dept Psychol & Mental Hlth, Kota SBY, Indonesia
[14] Univ Bern, Univ Hosp Child & Adolescent Psychiat & Psychothe, Bern, Switzerland
[15] Univ Munster, Inst Translat Psychiat, Munster, Germany
[16] Univ Lubeck, Dept Psychiat & Psycnotherapy, Lubeck, Germany
[17] Birmingham Womens & Childrens NHS Fdn Trust, Early Intervent Serv, Birmingham, W Midlands, England
[18] Univ Turku, Dept Psychiat, Turku, Finland
[19] Univ Melbourne, Dept Psychiat, Melbourne Neuropsychiat Ctr, Melbourne, Vic, Australia
[20] Orygen, Parkville, Vic, Australia
[21] Univ Melbourne, Ctr Youth Mental Hlth, Melbourne, Vic, Australia
[22] Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England
[23] Univ Milan, Dept Pathoplysiol & Transplantat, Milan, Italy
[24] Univ Basel, Dept Psychiat, Psychiat Univ Hosp, Univ Psychiat Clin Basel, Basel, Switzerland
基金
欧盟第七框架计划;
关键词
Machine learning; role functioning; personalised psychiatry; psychosis; PRONIA; MACHINE-LEARNING ALGORITHM; QUALITY-OF-LIFE; PSYCHOMETRIC PROPERTIES; CHILDHOOD TRAUMA; INDIVIDUALS; ADVERSITY; SCHIZOPHRENIA; PERSISTENCE; VALIDATION; CALCULATOR;
D O I
10.1192/bjp.2022.16
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Clinical high-risk states for psychosis (CHR) are associated with functional impairments and depressive disorders. A previous PRONIA study predicted social functioning in CHR and recent-onset depression (ROD) based on structural magnetic resonance imaging (sMRI) and clinical data. However, the combination of these domains did not lead to accurate role functioning prediction, calling for the investigation of additional risk dimensions. Role functioning may be more strongly associated with environmental adverse events than social functioning. Aims We aimed to predict role functioning in CHR, ROD and transdiagnostically, by adding environmental adverse events-related variables to clinical and sMRI data domains within the PRONIA sample. Method Baseline clinical, environmental and sMRI data collected in 92 CHR and 95 ROD samples were trained to predict lower versus higher follow-up role functioning, using support vector classification and mixed k-fold/leave-site-out cross-validation. We built separate predictions for each domain, created multimodal predictions and validated them in independent cohorts (74 CHR, 66 ROD). Results Models combining clinical and environmental data predicted role outcome in discovery and replication samples of CHR (balanced accuracies: 65.4% and 67.7%, respectively), ROD (balanced accuracies: 58.9% and 62.5%, respectively), and transdiagnostically (balanced accuracies: 62.4% and 68.2%, respectively). The most reliable environmental features for role outcome prediction were adult environmental adjustment, childhood trauma in CHR and childhood environmental adjustment in ROD. Conclusions Findings support the hypothesis that environmental variables inform role outcome prediction, highlight the existence of both transdiagnostic and syndrome-specific predictive environmental adverse events, and emphasise the importance of implementing real-world models by measuring multiple risk dimensions.
引用
收藏
页码:229 / 245
页数:17
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