Multimodal prognosis of negative symptom severity in individuals at increased risk of developing psychosis

被引:6
|
作者
Hauke, Daniel J. [1 ,2 ]
Schmidt, Andre [1 ]
Studerus, Erich [3 ]
Andreou, Christina [1 ,4 ]
Riecher-Roessler, Anita [1 ]
Radua, Joaquim [5 ,6 ,7 ]
Kambeitz, Joseph [8 ,9 ]
Ruef, Anne [10 ]
Dwyer, Dominic B. [10 ]
Kambeitz-Ilankovic, Lana [8 ,9 ,10 ]
Lichtenstein, Theresa [8 ,9 ]
Sanfelici, Rachele [10 ,11 ]
Penzel, Nora [8 ,9 ,10 ]
Haas, Shalaila S. [12 ]
Antonucci, Linda A. [13 ]
Lalousis, Paris Alexandros [14 ,15 ]
Chisholm, Katharine [14 ]
Schultze-Lutter, Frauke [16 ,17 ,18 ]
Ruhrmann, Stephan [8 ,9 ]
Hietala, Jarmo [19 ]
Brambilla, Paolo [20 ,21 ]
Koutsouleris, Nikolaos [10 ]
Meisenzahl, Eva [16 ]
Pantelis, Christos [22 ]
Rosen, Marlene [8 ,9 ]
Salokangas, Raimo K. R. [19 ]
Upthegrove, Rachel [14 ,23 ]
Wood, Stephen J. [14 ,24 ,25 ]
Borgwardt, Stefan [1 ,4 ]
机构
[1] Univ Basel, Dept Psychiat UPK, Basel, Switzerland
[2] Univ Basel, Dept Math & Comp Sci, Basel, Switzerland
[3] Univ Basel, Dept Psychol, Basel, Switzerland
[4] Univ Lubeck, Dept Psychiat & Psychotherapy, Lubeck, Germany
[5] CIBERSAM, Inst Invest Biomed August Pi i Sunyer IDIBAP, Imaging Mood & Anxiety Related Disorders IMARD Gr, Barcelona, Spain
[6] Kings Coll London, Inst Psychiat, Dept Psychosis Studies, Early Psychosis Intervent & Clin Detect EPIC Lab, London, England
[7] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[8] Univ Cologne, Fac Med, Dept Psychiat & Psychotherapy, Cologne, Germany
[9] Univ Cologne, Univ Hosp, Cologne, Germany
[10] Ludwig Maximilians Univ Munchen, Dept Psychiat & Psychotherapy, Munich, Germany
[11] Max Planck Sch Cognit, Leipzig, Germany
[12] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY USA
[13] Univ Bari Aldo Moro, Dept Educ, Psychol, Commun, Bari, Italy
[14] Univ Birmingham, Inst Mental Hlth, Birmingham, W Midlands, England
[15] Univ Birmingham, Ctr Human Brain Hlth, Birmingham, W Midlands, England
[16] Heinrich Heine Univ, Med Fac, Dept Psychiat & Psychotherapy, Dusseldorf, Germany
[17] Univ Bern, Univ Hosp Child & Adolescent Psychiat & Psychothe, Bern, Switzerland
[18] Airlangga Univ, Fac Psychol, Dept Psychol & Mental Hlth, Surabaya, Indonesia
[19] Univ Turku, Dept Psychiat, Turku, Finland
[20] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Neurosci & Mental Hlth, Milan, Italy
[21] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy
[22] Univ Melbourne & Melbourne Hlth, Melbourne Neuropsychiat Ctr, Carlton, Vic, Australia
[23] Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England
[24] Orygen, Melbourne, Vic, Australia
[25] Univ Melbourne, Ctr Youth Mental Hlth, Melbourne, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
CLINICAL HIGH-RISK; ULTRA-HIGH RISK; STRUCTURED INTERVIEW; MENTAL STATE; SCHIZOPHRENIA; PREDICTION; SYSTEM; PSYCHOPATHOLOGY; PSYCHIATRY; TRANSITION;
D O I
10.1038/s41398-021-01409-4
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Negative symptoms occur frequently in individuals at clinical high risk (CHR) for psychosis and contribute to functional impairments. The aim of this study was to predict negative symptom severity in CHR after 9 months. Predictive models either included baseline negative symptoms measured with the Structured Interview for Psychosis-Risk Syndromes (SIPS-N), whole-brain gyrification, or both to forecast negative symptoms of at least moderate severity in 94 CHR. We also conducted sequential risk stratification to stratify CHR into different risk groups based on the SIPS-N and gyrification model. Additionally, we assessed the models' ability to predict functional outcomes in CHR and their transdiagnostic generalizability to predict negative symptoms in 96 patients with recent-onset psychosis (ROP) and 97 patients with recent-onset depression (ROD). Baseline SIPS-N and gyrification predicted moderate/severe negative symptoms with significant balanced accuracies of 68 and 62%, while the combined model achieved 73% accuracy. Sequential risk stratification stratified CHR into a high (83%), medium (40-64%), and low (19%) risk group regarding their risk of having moderate/severe negative symptoms at 9 months follow-up. The baseline SIPS-N model was also able to predict social (61%), but not role functioning (59%) at above-chance accuracies, whereas the gyrification model achieved significant accuracies in predicting both social (76%) and role (74%) functioning in CHR. Finally, only the baseline SIPS-N model showed transdiagnostic generalization to ROP (63%). This study delivers a multimodal prognostic model to identify those CHR with a clinically relevant negative symptom severity and functional impairments, potentially requiring further therapeutic consideration.
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页数:11
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