Metabolic syndrome risk prediction in an Australian sample with first-episode psychosis using the psychosis metabolic risk calculator: A validation study

被引:0
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作者
Teasdale, Scott B. [1 ,2 ]
Ardill-Young, Oliver [1 ,2 ]
Morell, Rachel [1 ,2 ]
Ward, Philip B. [1 ,3 ,4 ]
Khandaker, Golam M. [5 ,6 ,7 ]
Upthegrove, Rachel [8 ,9 ,10 ]
Curtis, Jackie [1 ,2 ,11 ]
Perry, Benjamin, I [5 ,12 ]
机构
[1] UNSW Sydney, Sch Clin Med, Discipline Psychiat & Mental Hlth, High St, Kensington, NSW 2052, Australia
[2] Mindgardens Neurosci Network, Randwick, NSW, Australia
[3] Liverpool Hosp, South Western Sydney Local Hlth Dist, Schizophrenia Res Unit, Liverpool, NSW, Australia
[4] Liverpool Hosp, Ingham Inst Appl Med Res, Liverpool, NSW, Australia
[5] Univ Cambridge, Dept Psychiat, Trinity Lane, Cambridge CB2 1TN, England
[6] Univ Bristol, Ctr Acad Mental Hlth, Bristol Med Sch, Populat Hlth Sci, Bristol, England
[7] Univ Bristol, Bristol Med Sch, MRC Integrat Epidemiol Unit, Populat Hlth Sci, Bristol, England
[8] Univ Birmingham, Inst Mental Hlth, Birmingham, England
[9] Univ Birmingham, Ctr Human Brain Hlth, Birmingham, England
[10] Birmingham Womens & Childrens NHS Fdn Trust, Early Intervent Serv, Birmingham, England
[11] South Eastern Sydney Local Hlth Dist, Australia & Early Psychosis Programme, Bondi Jct, NSW, Australia
[12] Cambridgeshire & Peterborough NHS Fdn Trust, Dept Gen Psychiat, Cambridge, England
基金
英国医学研究理事会; 芬兰科学院; 英国惠康基金;
关键词
mental disorders; psychosis; antipsychotic; metabolic syndrome; risk prediction; validation study; CARDIOMETABOLIC RISK; CONSENSUS STATEMENT; YOUNG-PEOPLE; SCHIZOPHRENIA; HEALTH;
D O I
10.1177/10398562241269171
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective To examine the accuracy and likely clinical usefulness of the Psychosis Metabolic Risk Calculator (PsyMetRiC) in predicting up-to six-year risk of incident metabolic syndrome in an Australian sample of young people with first-episode psychosis.Method We conducted a retrospective study at a secondary care early psychosis treatment service among people aged 16-35 years, extracting relevant data at the time of antipsychotic commencement and between one-to-six-years later. We assessed algorithm accuracy primarily via discrimination (C-statistic), calibration (calibration plots) and clinical usefulness (decision curve analysis). Model updating and recalibration generated a site-specific (Australian) PsyMetRiC version.Results We included 116 people with baseline and follow-up data: 73% male, mean age 20.1 years, mean follow-up 2.6 years, metabolic syndrome prevalence 13%. C-statistics for both partial- (C = 0.71, 95% CI 0.64-0.75) and full-models (C = 0.72, 95% CI 0.65-0.77) were acceptable; however, calibration plots demonstrated consistent under-prediction of risk. Recalibration and updating led to slightly improved C-statistics, greatly improved agreement between observed and predicted risk, and a narrow window of likely clinical usefulness improved significantly.Conclusion An updated and recalibrated PsyMetRiC model, PsyMetRiC-Australia, shows promise. Validation in a large sample is required to confirm its accuracy and clinical usefulness for the Australian population.
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页数:8
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