Prediction of Early Symptom Remission in Two Independent Samples of First-Episode Psychosis Patients Using Machine Learning
Abstract Background Validated clinical prediction models of short-term remission in psychosis are lacking. Our aim was to develop a clinical prediction model aimed at predicting 4−6-week remission following a first episode of psychosis. Method Baseline clinical data from the Athens First Episode Res...
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Veröffentlicht in: | Schizophrenia bulletin 2022-01, Vol.48 (1), p.122-133 |
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creator | Soldatos, Rigas F Cearns, Micah Nielsen, Mette Ø Kollias, Costas Xenaki, Lida-Alkisti Stefanatou, Pentagiotissa Ralli, Irene Dimitrakopoulos, Stefanos Hatzimanolis, Alex Kosteletos, Ioannis Vlachos, Ilias I Selakovic, Mirjana Foteli, Stefania Nianiakas, Nikolaos Mantonakis, Leonidas Triantafyllou, Theoni F Ntigridaki, Aggeliki Ermiliou, Vanessa Voulgaraki, Marina Psarra, Evaggelia Sørensen, Mikkel E Bojesen, Kirsten B Tangmose, Karen Sigvard, Anne M Ambrosen, Karen S Meritt, Toni Syeda, Warda Glenthøj, Birte Y Koutsouleris, Nikolaos Pantelis, Christos Ebdrup, Bjørn H Stefanis, Nikos |
description | Abstract
Background
Validated clinical prediction models of short-term remission in psychosis are lacking. Our aim was to develop a clinical prediction model aimed at predicting 4−6-week remission following a first episode of psychosis.
Method
Baseline clinical data from the Athens First Episode Research Study was used to develop a Support Vector Machine prediction model of 4-week symptom remission in first-episode psychosis patients using repeated nested cross-validation. This model was further tested to predict 6-week remission in a sample of two independent, consecutive Danish first-episode cohorts.
Results
Of the 179 participants in Athens, 120 were male with an average age of 25.8 years and average duration of untreated psychosis of 32.8 weeks. 62.9% were antipsychotic-naïve. Fifty-seven percent attained remission after 4 weeks. In the Danish cohort, 31% attained remission. Eleven clinical scale items were selected in the Athens 4-week remission cohort. These included the Duration of Untreated Psychosis, Personal and Social Performance Scale, Global Assessment of Functioning and eight items from the Positive and Negative Syndrome Scale. This model significantly predicted 4-week remission status (area under the receiver operator characteristic curve (ROC-AUC) = 71.45, P < .0001). It also predicted 6-week remission status in the Danish cohort (ROC-AUC = 67.74, P < .0001), demonstrating reliability.
Conclusions
Using items from common and validated clinical scales, our model significantly predicted early remission in patients with first-episode psychosis. Although replicated in an independent cohort, forward testing between machine learning models and clinicians’ assessment should be undertaken to evaluate the possible utility as a routine clinical tool. |
doi_str_mv | 10.1093/schbul/sbab107 |
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Background
Validated clinical prediction models of short-term remission in psychosis are lacking. Our aim was to develop a clinical prediction model aimed at predicting 4−6-week remission following a first episode of psychosis.
Method
Baseline clinical data from the Athens First Episode Research Study was used to develop a Support Vector Machine prediction model of 4-week symptom remission in first-episode psychosis patients using repeated nested cross-validation. This model was further tested to predict 6-week remission in a sample of two independent, consecutive Danish first-episode cohorts.
Results
Of the 179 participants in Athens, 120 were male with an average age of 25.8 years and average duration of untreated psychosis of 32.8 weeks. 62.9% were antipsychotic-naïve. Fifty-seven percent attained remission after 4 weeks. In the Danish cohort, 31% attained remission. Eleven clinical scale items were selected in the Athens 4-week remission cohort. These included the Duration of Untreated Psychosis, Personal and Social Performance Scale, Global Assessment of Functioning and eight items from the Positive and Negative Syndrome Scale. This model significantly predicted 4-week remission status (area under the receiver operator characteristic curve (ROC-AUC) = 71.45, P < .0001). It also predicted 6-week remission status in the Danish cohort (ROC-AUC = 67.74, P < .0001), demonstrating reliability.
Conclusions
Using items from common and validated clinical scales, our model significantly predicted early remission in patients with first-episode psychosis. Although replicated in an independent cohort, forward testing between machine learning models and clinicians’ assessment should be undertaken to evaluate the possible utility as a routine clinical tool.</description><identifier>ISSN: 0586-7614</identifier><identifier>EISSN: 1745-1701</identifier><identifier>DOI: 10.1093/schbul/sbab107</identifier><identifier>PMID: 34535800</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adolescent ; Adult ; Cohort Studies ; Female ; Humans ; Male ; Models, Statistical ; Outcome Assessment, Health Care - methods ; Prognosis ; Psychotic Disorders - diagnosis ; Psychotic Disorders - physiopathology ; Psychotic Disorders - therapy ; Regular ; Remission Induction ; Remission, Spontaneous ; Schizophrenia - diagnosis ; Schizophrenia - physiopathology ; Schizophrenia - therapy ; Support Vector Machine ; Young Adult</subject><ispartof>Schizophrenia bulletin, 2022-01, Vol.48 (1), p.122-133</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center.All rights reserved. For permissions, please email: journals.permissions@oup.com 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center.All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-10be7b84d30f0804ee41b7288e32c24b9833e4197e39281b878d96c91c39e8ed3</citedby><cites>FETCH-LOGICAL-c424t-10be7b84d30f0804ee41b7288e32c24b9833e4197e39281b878d96c91c39e8ed3</cites><orcidid>0000-0001-8337-5366 ; 0000-0002-6623-7225 ; 0000-0001-9044-7081 ; 0000-0002-9565-0238</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781312/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781312/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,1585,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34535800$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soldatos, Rigas F</creatorcontrib><creatorcontrib>Cearns, Micah</creatorcontrib><creatorcontrib>Nielsen, Mette Ø</creatorcontrib><creatorcontrib>Kollias, Costas</creatorcontrib><creatorcontrib>Xenaki, Lida-Alkisti</creatorcontrib><creatorcontrib>Stefanatou, Pentagiotissa</creatorcontrib><creatorcontrib>Ralli, Irene</creatorcontrib><creatorcontrib>Dimitrakopoulos, Stefanos</creatorcontrib><creatorcontrib>Hatzimanolis, Alex</creatorcontrib><creatorcontrib>Kosteletos, Ioannis</creatorcontrib><creatorcontrib>Vlachos, Ilias I</creatorcontrib><creatorcontrib>Selakovic, Mirjana</creatorcontrib><creatorcontrib>Foteli, Stefania</creatorcontrib><creatorcontrib>Nianiakas, Nikolaos</creatorcontrib><creatorcontrib>Mantonakis, Leonidas</creatorcontrib><creatorcontrib>Triantafyllou, Theoni F</creatorcontrib><creatorcontrib>Ntigridaki, Aggeliki</creatorcontrib><creatorcontrib>Ermiliou, Vanessa</creatorcontrib><creatorcontrib>Voulgaraki, Marina</creatorcontrib><creatorcontrib>Psarra, Evaggelia</creatorcontrib><creatorcontrib>Sørensen, Mikkel E</creatorcontrib><creatorcontrib>Bojesen, Kirsten B</creatorcontrib><creatorcontrib>Tangmose, Karen</creatorcontrib><creatorcontrib>Sigvard, Anne M</creatorcontrib><creatorcontrib>Ambrosen, Karen S</creatorcontrib><creatorcontrib>Meritt, Toni</creatorcontrib><creatorcontrib>Syeda, Warda</creatorcontrib><creatorcontrib>Glenthøj, Birte Y</creatorcontrib><creatorcontrib>Koutsouleris, Nikolaos</creatorcontrib><creatorcontrib>Pantelis, Christos</creatorcontrib><creatorcontrib>Ebdrup, Bjørn H</creatorcontrib><creatorcontrib>Stefanis, Nikos</creatorcontrib><title>Prediction of Early Symptom Remission in Two Independent Samples of First-Episode Psychosis Patients Using Machine Learning</title><title>Schizophrenia bulletin</title><addtitle>Schizophr Bull</addtitle><description>Abstract
Background
Validated clinical prediction models of short-term remission in psychosis are lacking. Our aim was to develop a clinical prediction model aimed at predicting 4−6-week remission following a first episode of psychosis.
Method
Baseline clinical data from the Athens First Episode Research Study was used to develop a Support Vector Machine prediction model of 4-week symptom remission in first-episode psychosis patients using repeated nested cross-validation. This model was further tested to predict 6-week remission in a sample of two independent, consecutive Danish first-episode cohorts.
Results
Of the 179 participants in Athens, 120 were male with an average age of 25.8 years and average duration of untreated psychosis of 32.8 weeks. 62.9% were antipsychotic-naïve. Fifty-seven percent attained remission after 4 weeks. In the Danish cohort, 31% attained remission. Eleven clinical scale items were selected in the Athens 4-week remission cohort. These included the Duration of Untreated Psychosis, Personal and Social Performance Scale, Global Assessment of Functioning and eight items from the Positive and Negative Syndrome Scale. This model significantly predicted 4-week remission status (area under the receiver operator characteristic curve (ROC-AUC) = 71.45, P < .0001). It also predicted 6-week remission status in the Danish cohort (ROC-AUC = 67.74, P < .0001), demonstrating reliability.
Conclusions
Using items from common and validated clinical scales, our model significantly predicted early remission in patients with first-episode psychosis. Although replicated in an independent cohort, forward testing between machine learning models and clinicians’ assessment should be undertaken to evaluate the possible utility as a routine clinical tool.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Models, Statistical</subject><subject>Outcome Assessment, Health Care - methods</subject><subject>Prognosis</subject><subject>Psychotic Disorders - diagnosis</subject><subject>Psychotic Disorders - physiopathology</subject><subject>Psychotic Disorders - therapy</subject><subject>Regular</subject><subject>Remission Induction</subject><subject>Remission, Spontaneous</subject><subject>Schizophrenia - diagnosis</subject><subject>Schizophrenia - physiopathology</subject><subject>Schizophrenia - therapy</subject><subject>Support Vector Machine</subject><subject>Young Adult</subject><issn>0586-7614</issn><issn>1745-1701</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhyhH5CIe0duzEzgUJVVuotKirfpwt25ntGiVx8CRUq_55vNqlghMXW5p55vHILyHvOTvjrBHn6Ldu7s7RWceZekEWXMmq4Irxl2TBKl0XqubyhLxB_MEYl01dviYnQlai0owtyNM6QRv8FOJA44Yubep29HbXj1Ps6Q30AXHfCgO9e4z0amhhhHwME721_dgB7qcuQ8KpWI4BYwt0jTu_jRiQru0UMor0HsPwQL9bvw0D0BXYNOTCW_JqYzuEd8f7lNxfLu8uvhWr669XF19WhZelnArOHCinZSvYhmkmASR3qtQaROlL6RotRC41CkRTau600m1T-4Z70YCGVpySzwfvOLseWp9XSrYzYwq9TTsTbTD_doawNQ_xl8kmLniZBR-PghR_zoCTyf_ioevsAHFGU1ZKSlZzzjJ6dkB9iogJNs_PcGb2iZlDYuaYWB748Pdyz_ifiDLw6QDEefyf7Dda8KTM</recordid><startdate>20220121</startdate><enddate>20220121</enddate><creator>Soldatos, Rigas F</creator><creator>Cearns, Micah</creator><creator>Nielsen, Mette Ø</creator><creator>Kollias, Costas</creator><creator>Xenaki, Lida-Alkisti</creator><creator>Stefanatou, Pentagiotissa</creator><creator>Ralli, Irene</creator><creator>Dimitrakopoulos, Stefanos</creator><creator>Hatzimanolis, Alex</creator><creator>Kosteletos, Ioannis</creator><creator>Vlachos, Ilias I</creator><creator>Selakovic, Mirjana</creator><creator>Foteli, Stefania</creator><creator>Nianiakas, Nikolaos</creator><creator>Mantonakis, Leonidas</creator><creator>Triantafyllou, Theoni F</creator><creator>Ntigridaki, Aggeliki</creator><creator>Ermiliou, Vanessa</creator><creator>Voulgaraki, Marina</creator><creator>Psarra, Evaggelia</creator><creator>Sørensen, Mikkel E</creator><creator>Bojesen, Kirsten B</creator><creator>Tangmose, Karen</creator><creator>Sigvard, Anne M</creator><creator>Ambrosen, Karen S</creator><creator>Meritt, Toni</creator><creator>Syeda, Warda</creator><creator>Glenthøj, Birte Y</creator><creator>Koutsouleris, Nikolaos</creator><creator>Pantelis, Christos</creator><creator>Ebdrup, Bjørn H</creator><creator>Stefanis, Nikos</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8337-5366</orcidid><orcidid>https://orcid.org/0000-0002-6623-7225</orcidid><orcidid>https://orcid.org/0000-0001-9044-7081</orcidid><orcidid>https://orcid.org/0000-0002-9565-0238</orcidid></search><sort><creationdate>20220121</creationdate><title>Prediction of Early Symptom Remission in Two Independent Samples of First-Episode Psychosis Patients Using Machine Learning</title><author>Soldatos, Rigas F ; Cearns, Micah ; Nielsen, Mette Ø ; Kollias, Costas ; Xenaki, Lida-Alkisti ; Stefanatou, Pentagiotissa ; Ralli, Irene ; Dimitrakopoulos, Stefanos ; Hatzimanolis, Alex ; Kosteletos, Ioannis ; Vlachos, Ilias I ; Selakovic, Mirjana ; Foteli, Stefania ; Nianiakas, Nikolaos ; Mantonakis, Leonidas ; Triantafyllou, Theoni F ; Ntigridaki, Aggeliki ; Ermiliou, Vanessa ; Voulgaraki, Marina ; Psarra, Evaggelia ; Sørensen, Mikkel E ; Bojesen, Kirsten B ; Tangmose, Karen ; Sigvard, Anne M ; Ambrosen, Karen S ; Meritt, Toni ; Syeda, Warda ; Glenthøj, Birte Y ; Koutsouleris, Nikolaos ; Pantelis, Christos ; Ebdrup, Bjørn H ; Stefanis, Nikos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-10be7b84d30f0804ee41b7288e32c24b9833e4197e39281b878d96c91c39e8ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Models, Statistical</topic><topic>Outcome Assessment, Health Care - methods</topic><topic>Prognosis</topic><topic>Psychotic Disorders - diagnosis</topic><topic>Psychotic Disorders - physiopathology</topic><topic>Psychotic Disorders - therapy</topic><topic>Regular</topic><topic>Remission Induction</topic><topic>Remission, Spontaneous</topic><topic>Schizophrenia - diagnosis</topic><topic>Schizophrenia - physiopathology</topic><topic>Schizophrenia - therapy</topic><topic>Support Vector Machine</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soldatos, Rigas F</creatorcontrib><creatorcontrib>Cearns, Micah</creatorcontrib><creatorcontrib>Nielsen, Mette Ø</creatorcontrib><creatorcontrib>Kollias, Costas</creatorcontrib><creatorcontrib>Xenaki, Lida-Alkisti</creatorcontrib><creatorcontrib>Stefanatou, Pentagiotissa</creatorcontrib><creatorcontrib>Ralli, Irene</creatorcontrib><creatorcontrib>Dimitrakopoulos, Stefanos</creatorcontrib><creatorcontrib>Hatzimanolis, Alex</creatorcontrib><creatorcontrib>Kosteletos, Ioannis</creatorcontrib><creatorcontrib>Vlachos, Ilias I</creatorcontrib><creatorcontrib>Selakovic, Mirjana</creatorcontrib><creatorcontrib>Foteli, Stefania</creatorcontrib><creatorcontrib>Nianiakas, Nikolaos</creatorcontrib><creatorcontrib>Mantonakis, Leonidas</creatorcontrib><creatorcontrib>Triantafyllou, Theoni F</creatorcontrib><creatorcontrib>Ntigridaki, Aggeliki</creatorcontrib><creatorcontrib>Ermiliou, Vanessa</creatorcontrib><creatorcontrib>Voulgaraki, Marina</creatorcontrib><creatorcontrib>Psarra, Evaggelia</creatorcontrib><creatorcontrib>Sørensen, Mikkel E</creatorcontrib><creatorcontrib>Bojesen, Kirsten B</creatorcontrib><creatorcontrib>Tangmose, Karen</creatorcontrib><creatorcontrib>Sigvard, Anne M</creatorcontrib><creatorcontrib>Ambrosen, Karen S</creatorcontrib><creatorcontrib>Meritt, Toni</creatorcontrib><creatorcontrib>Syeda, Warda</creatorcontrib><creatorcontrib>Glenthøj, Birte Y</creatorcontrib><creatorcontrib>Koutsouleris, Nikolaos</creatorcontrib><creatorcontrib>Pantelis, Christos</creatorcontrib><creatorcontrib>Ebdrup, Bjørn H</creatorcontrib><creatorcontrib>Stefanis, Nikos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Schizophrenia bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soldatos, Rigas F</au><au>Cearns, Micah</au><au>Nielsen, Mette Ø</au><au>Kollias, Costas</au><au>Xenaki, Lida-Alkisti</au><au>Stefanatou, Pentagiotissa</au><au>Ralli, Irene</au><au>Dimitrakopoulos, Stefanos</au><au>Hatzimanolis, Alex</au><au>Kosteletos, Ioannis</au><au>Vlachos, Ilias I</au><au>Selakovic, Mirjana</au><au>Foteli, Stefania</au><au>Nianiakas, Nikolaos</au><au>Mantonakis, Leonidas</au><au>Triantafyllou, Theoni F</au><au>Ntigridaki, Aggeliki</au><au>Ermiliou, Vanessa</au><au>Voulgaraki, Marina</au><au>Psarra, Evaggelia</au><au>Sørensen, Mikkel E</au><au>Bojesen, Kirsten B</au><au>Tangmose, Karen</au><au>Sigvard, Anne M</au><au>Ambrosen, Karen S</au><au>Meritt, Toni</au><au>Syeda, Warda</au><au>Glenthøj, Birte Y</au><au>Koutsouleris, Nikolaos</au><au>Pantelis, Christos</au><au>Ebdrup, Bjørn H</au><au>Stefanis, Nikos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of Early Symptom Remission in Two Independent Samples of First-Episode Psychosis Patients Using Machine Learning</atitle><jtitle>Schizophrenia bulletin</jtitle><addtitle>Schizophr Bull</addtitle><date>2022-01-21</date><risdate>2022</risdate><volume>48</volume><issue>1</issue><spage>122</spage><epage>133</epage><pages>122-133</pages><issn>0586-7614</issn><eissn>1745-1701</eissn><abstract>Abstract
Background
Validated clinical prediction models of short-term remission in psychosis are lacking. Our aim was to develop a clinical prediction model aimed at predicting 4−6-week remission following a first episode of psychosis.
Method
Baseline clinical data from the Athens First Episode Research Study was used to develop a Support Vector Machine prediction model of 4-week symptom remission in first-episode psychosis patients using repeated nested cross-validation. This model was further tested to predict 6-week remission in a sample of two independent, consecutive Danish first-episode cohorts.
Results
Of the 179 participants in Athens, 120 were male with an average age of 25.8 years and average duration of untreated psychosis of 32.8 weeks. 62.9% were antipsychotic-naïve. Fifty-seven percent attained remission after 4 weeks. In the Danish cohort, 31% attained remission. Eleven clinical scale items were selected in the Athens 4-week remission cohort. These included the Duration of Untreated Psychosis, Personal and Social Performance Scale, Global Assessment of Functioning and eight items from the Positive and Negative Syndrome Scale. This model significantly predicted 4-week remission status (area under the receiver operator characteristic curve (ROC-AUC) = 71.45, P < .0001). It also predicted 6-week remission status in the Danish cohort (ROC-AUC = 67.74, P < .0001), demonstrating reliability.
Conclusions
Using items from common and validated clinical scales, our model significantly predicted early remission in patients with first-episode psychosis. Although replicated in an independent cohort, forward testing between machine learning models and clinicians’ assessment should be undertaken to evaluate the possible utility as a routine clinical tool.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>34535800</pmid><doi>10.1093/schbul/sbab107</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8337-5366</orcidid><orcidid>https://orcid.org/0000-0002-6623-7225</orcidid><orcidid>https://orcid.org/0000-0001-9044-7081</orcidid><orcidid>https://orcid.org/0000-0002-9565-0238</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); PubMed Central; Alma/SFX Local Collection |
subjects | Adolescent Adult Cohort Studies Female Humans Male Models, Statistical Outcome Assessment, Health Care - methods Prognosis Psychotic Disorders - diagnosis Psychotic Disorders - physiopathology Psychotic Disorders - therapy Regular Remission Induction Remission, Spontaneous Schizophrenia - diagnosis Schizophrenia - physiopathology Schizophrenia - therapy Support Vector Machine Young Adult |
title | Prediction of Early Symptom Remission in Two Independent Samples of First-Episode Psychosis Patients Using Machine Learning |
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