Real-world digital implementation of the Psychosis Polyrisk Score (PPS): A pilot feasibility study

被引:13
|
作者
Oliver, Dominic [1 ,2 ]
Spada, Giulia [1 ,2 ]
Englund, Amir [3 ]
Chesney, Edward [3 ]
Radua, Joaquim [1 ,4 ,5 ]
Reichenberg, Abraham [3 ,6 ,7 ,8 ]
Uher, Rudolf [9 ]
McGuire, Philip [3 ]
Fusar-Poli, Paolo [1 ,2 ,10 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, Early Psychosis Intervent & Clin Detect EPIC Lab, London, England
[2] South London & Maudsley NHS Fdn Trust, OASIS Serv, London, England
[3] Kings Coll London, Inst Psychiat Psychol & Neurosci, London, England
[4] CIBERSAM, Inst Invest Biomed August Pi & Sunyer IDIBAPS, Imaging Mood & Anxiety Related Disorders IMARD, Barcelona, Spain
[5] Karolinska Inst, Ctr Psychiat Res, Dept Clin Neurosci, Stockholm, Sweden
[6] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY USA
[7] Icahn Sch Med Mt Sinai, Dept Environm Med & Publ Hlth, New York, NY USA
[8] Icahn Sch Med Mt Sinai, Frieman Brain Inst, New York, NY USA
[9] Dalhousie Univ, Dept Psychiat, Halifax, NS, Canada
[10] Univ Pavia, Dept Brain & Behav Sci, Pavia, Italy
基金
英国医学研究理事会;
关键词
Clinical high risk; Risk; Prediction; Environment; Polygenic risk; Implementation; CLINICAL HIGH-RISK; 1ST-EPISODE PSYCHOSIS; PROGNOSTIC ACCURACY; MENTAL STATES; HELP-SEEKING; INDIVIDUALS; PREDICTION; SCHIZOPHRENIA; METAANALYSIS; CALCULATOR;
D O I
10.1016/j.schres.2020.04.015
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: The Psychosis Polyrisk Score (PPS) is a potential biomarker integrating non-purely genetic risk/protective factors for psychosis that may improve identification of individuals at risk and prediction of their outcomes at the individual subject level. Biomarkers that are easy to administer are direly needed in early psychosis to facilitate clinical implementation. This study digitally implements the PPS and pilots its feasibility of use in the real world. Methods: The PPS was implemented digitally and prospectively piloted across individuals referred for a CHR-P assessment (n=16) and healthy controls (n=66). Distribution of PPS scores was further simulated in the general population. Results: 98.8% of individuals referred for a CHR-P assessment and healthy controls completed the PPS assessment with only one drop-out. 96.3% of participants completed the assessment in under 15 min. Individuals referred for a CHR-P assessment had high PPS scores (mean=6.2, SD=7.23) than healthy controls (mean=-1.79, SD=6.78, p < 0.001). In simulated general population data, scores were normally distributed ranging from -15 (lowest risk, RR=0.03) to 39.5 (highest risk, RR=8912.51). Discussion: The PPS is a promising biomarker which has been implemented digitally. The PPS can be easily administered to both healthy controls and individuals at potential risk for psychosis on a range of devices. It is feasible to use the PPS in real world settings to assess individuals with emerging mental disorders. The next phase of research should be to include the PPS in large-scale international cohort studies to evaluate its ability to refine the prognostication of outcomes. (C) 2020 The Authors. Published by Elsevier B.V.
引用
收藏
页码:176 / 183
页数:8
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