S219. SINGLE-SUBJECT PREDICTION OF FUNCTIONAL OUTCOMES ACROSS DIAGNOSTIC GROUPS USING CLINICAL DATA
BackgroundPsychotic disorders are associated with serious deterioration in functioning even before the first psychotic episode. Also on clinical high risk (CHR) states of developing a first psychotic episode, several studies reported a decreased global functioning. In a considerable proportion of CH...
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Published in | Schizophrenia bulletin Vol. 46; no. Supplement_1; p. S122 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
US
Oxford University Press
18.05.2020
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Subjects | |
Online Access | Get full text |
ISSN | 0586-7614 1745-1701 |
DOI | 10.1093/schbul/sbaa031.285 |
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Abstract | BackgroundPsychotic disorders are associated with serious deterioration in functioning even before the first psychotic episode. Also on clinical high risk (CHR) states of developing a first psychotic episode, several studies reported a decreased global functioning. In a considerable proportion of CHR individuals, functional deterioration remains even after (transient) remission of symptomatic risk indicators. Furthermore, deficits in functioning cause immense costs for the health care system and are often more debilitating for individuals than positive symptoms. However in the past, CHR research has mostly focused on clinical outcomes like transition. Prediction of functioning in CHR populations has received less attention. Therefore, the current study aims at predicting functioning in CHR individuals at a single subject level applying multi pattern recognition to clinical data. Patients with a first depressive episode who frequently have persistent functional deficits comparable to patients in the CHR state were investigated in addition.MethodsPRONIA (‘Personalized Prognostic Tools for Early Psychosis Management’) is a prospective collaboration project funded by the European Union under the 7th Framework Programme (grant agreement n°602152). Considering a broad set of variables (MRI, clinical data, neurocognition, genomics and other blood derived parameters) as well as advanced statistical methods, PRONIA aims at developing an innovative multivariate prognostic tool enabling an individualized prediction of illness trajectories and outcome. 11 university centers in five European countries and in Australia (Munich, Basel, Birmingham, Cologne, Düsseldorf, Münster, Melbourne, Milan, Udine, Bari, Turku) participate in the evaluation of three clinical groups (subjects clinically at high risk of developing a psychosis [CHR], patients with a recent onset psychosis [ROP] and patients with a recent onset depression [ROD]) as well as healthy controls.In the current study, we analysed data of 114 CHR and 106 ROD patients. Functioning was measured by the ‘Global Functioning: Social and Role’ Scales (GF S/R). In a repeated, nested cross validation framework we trained a l1-regularized SVM to predict good versus bad outcome. Multivariate pattern recognition analysis allowed to identify most predictive variables from a multitude of clinical, environmental as well as sociodemographic potential predictors assessed in PRONIA.ResultsBased on the 5 to 20 identified most predictive features, prediction models revealed a balanced accuracy (BAC) up to 77/72 for social functioning in CHR/ROD patients and up to 73/69 for role functioning. These models showed satisfying performance of BACs up to 69/63 for social functioning and 67/60 for role functioning in an independent test sample. As expected, prior functioning levels were identified as main predictive factor but also distinct protective and risk factors were selected into the prediction models.DiscussionResults suggest that especially prediction of the multi-faceted construct of role functioning could benefit from inclusion of a rich set of clinical variables.To the best of our knowledge this is the first study that has validated clinical prediction models of functioning in an independent test sample. Identification of predictive variables enables a much more efficient prognostic process. Moreover, understanding the mechanisms underlying functional decline and its illness related pattern might enable an improved definition of targets for intervention. Future research should aim at further maximisation of prediction accuracy and cross-centre generalisation capacity. In addition, other functioning outcomes as well as clinical outcomes need to be focused on. |
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AbstractList | BackgroundPsychotic disorders are associated with serious deterioration in functioning even before the first psychotic episode. Also on clinical high risk (CHR) states of developing a first psychotic episode, several studies reported a decreased global functioning. In a considerable proportion of CHR individuals, functional deterioration remains even after (transient) remission of symptomatic risk indicators. Furthermore, deficits in functioning cause immense costs for the health care system and are often more debilitating for individuals than positive symptoms. However in the past, CHR research has mostly focused on clinical outcomes like transition. Prediction of functioning in CHR populations has received less attention. Therefore, the current study aims at predicting functioning in CHR individuals at a single subject level applying multi pattern recognition to clinical data. Patients with a first depressive episode who frequently have persistent functional deficits comparable to patients in the CHR state were investigated in addition.MethodsPRONIA (‘Personalized Prognostic Tools for Early Psychosis Management’) is a prospective collaboration project funded by the European Union under the 7th Framework Programme (grant agreement n°602152). Considering a broad set of variables (MRI, clinical data, neurocognition, genomics and other blood derived parameters) as well as advanced statistical methods, PRONIA aims at developing an innovative multivariate prognostic tool enabling an individualized prediction of illness trajectories and outcome. 11 university centers in five European countries and in Australia (Munich, Basel, Birmingham, Cologne, Düsseldorf, Münster, Melbourne, Milan, Udine, Bari, Turku) participate in the evaluation of three clinical groups (subjects clinically at high risk of developing a psychosis [CHR], patients with a recent onset psychosis [ROP] and patients with a recent onset depression [ROD]) as well as healthy controls.In the current study, we analysed data of 114 CHR and 106 ROD patients. Functioning was measured by the ‘Global Functioning: Social and Role’ Scales (GF S/R). In a repeated, nested cross validation framework we trained a l1-regularized SVM to predict good versus bad outcome. Multivariate pattern recognition analysis allowed to identify most predictive variables from a multitude of clinical, environmental as well as sociodemographic potential predictors assessed in PRONIA.ResultsBased on the 5 to 20 identified most predictive features, prediction models revealed a balanced accuracy (BAC) up to 77/72 for social functioning in CHR/ROD patients and up to 73/69 for role functioning. These models showed satisfying performance of BACs up to 69/63 for social functioning and 67/60 for role functioning in an independent test sample. As expected, prior functioning levels were identified as main predictive factor but also distinct protective and risk factors were selected into the prediction models.DiscussionResults suggest that especially prediction of the multi-faceted construct of role functioning could benefit from inclusion of a rich set of clinical variables.To the best of our knowledge this is the first study that has validated clinical prediction models of functioning in an independent test sample. Identification of predictive variables enables a much more efficient prognostic process. Moreover, understanding the mechanisms underlying functional decline and its illness related pattern might enable an improved definition of targets for intervention. Future research should aim at further maximisation of prediction accuracy and cross-centre generalisation capacity. In addition, other functioning outcomes as well as clinical outcomes need to be focused on. |
Author | Schultze-Lutter, Frauke Chisholm, Katharine Rosen, Marlene Haidl, Theresa Pilgram, Tanja Kambeitz, Joseph Bertolino, Alessandro Brambilla, Paolo Upthegrove, Rachel Salokangas, Raimo K R Wood, Stephen Kaiser, Nathalie Seves, Mauro Borgwardt, Stefan Lencer, Rebekka Meisenzahl, Eva Koutsouleris, Nikolaos Betz, Linda Ruhrmann, Stephan |
AuthorAffiliation | 2 Heinrich-Heine University Düsseldorf 5 University of Basel 9 Orygen, the National Centre of Excellence in Youth Mental Health 10 Ludwig-Maximilian-University 4 University of Bari 3 University of Birmingham 6 University of Milan, Italy 8 University of Turku, Finland 7 Münster University 1 University Cologne , Germany 11 PRONIA |
AuthorAffiliation_xml | – name: 8 University of Turku, Finland – name: 10 Ludwig-Maximilian-University – name: 5 University of Basel – name: 2 Heinrich-Heine University Düsseldorf – name: 7 Münster University – name: 3 University of Birmingham – name: 4 University of Bari – name: 9 Orygen, the National Centre of Excellence in Youth Mental Health – name: 1 University Cologne , Germany – name: 6 University of Milan, Italy – name: 11 PRONIA |
Author_xml | – sequence: 1 givenname: Marlene surname: Rosen fullname: Rosen, Marlene organization: University Cologne, Germany – sequence: 2 givenname: Nathalie surname: Kaiser fullname: Kaiser, Nathalie organization: University Cologne, Germany – sequence: 3 givenname: Linda surname: Betz fullname: Betz, Linda organization: University Cologne, Germany – sequence: 4 givenname: Theresa surname: Haidl fullname: Haidl, Theresa organization: University Cologne, Germany – sequence: 5 givenname: Mauro surname: Seves fullname: Seves, Mauro organization: University Cologne, Germany – sequence: 6 givenname: Tanja surname: Pilgram fullname: Pilgram, Tanja organization: University Cologne, Germany – sequence: 7 givenname: Frauke surname: Schultze-Lutter fullname: Schultze-Lutter, Frauke organization: Heinrich-Heine University Düsseldorf – sequence: 8 givenname: Katharine surname: Chisholm fullname: Chisholm, Katharine organization: University of Birmingham – sequence: 9 givenname: Alessandro surname: Bertolino fullname: Bertolino, Alessandro organization: University of Bari – sequence: 10 givenname: Stefan surname: Borgwardt fullname: Borgwardt, Stefan organization: University of Basel – sequence: 11 givenname: Paolo surname: Brambilla fullname: Brambilla, Paolo organization: University of Milan, Italy – sequence: 12 givenname: Rebekka surname: Lencer fullname: Lencer, Rebekka organization: Münster University – sequence: 13 givenname: Eva surname: Meisenzahl fullname: Meisenzahl, Eva organization: Heinrich-Heine University Düsseldorf – sequence: 14 givenname: Stephan surname: Ruhrmann fullname: Ruhrmann, Stephan organization: University Cologne, Germany – sequence: 15 givenname: Raimo K R surname: Salokangas fullname: Salokangas, Raimo K R organization: University of Turku, Finland – sequence: 16 givenname: Rachel surname: Upthegrove fullname: Upthegrove, Rachel organization: University of Birmingham – sequence: 17 givenname: Stephen surname: Wood fullname: Wood, Stephen organization: Orygen, the National Centre of Excellence in Youth Mental Health – sequence: 18 givenname: Nikolaos surname: Koutsouleris fullname: Koutsouleris, Nikolaos organization: Ludwig-Maximilian-University – sequence: 19 givenname: Joseph surname: Kambeitz fullname: Kambeitz, Joseph organization: University Cologne, Germany |
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Copyright | The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. 2020 The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Title | S219. SINGLE-SUBJECT PREDICTION OF FUNCTIONAL OUTCOMES ACROSS DIAGNOSTIC GROUPS USING CLINICAL DATA |
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