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Psychosis metabolic risk calculator (PsyMetRiC) in early psychosis: External validation study in Finland

Keinänen, Jaakko; Eskelinen, Saana; From, Tiina; Laurikainen, Heikki; Hietala, Jarmo; Murray, Graham K.; Suvisaari, Jaana; Perry, Benjamin I.

Psychosis metabolic risk calculator (PsyMetRiC) in early psychosis: External validation study in Finland

Keinänen, Jaakko
Eskelinen, Saana
From, Tiina
Laurikainen, Heikki
Hietala, Jarmo
Murray, Graham K.
Suvisaari, Jaana
Perry, Benjamin I.
Katso/Avaa
Acta Psychiatr Scand - 2024 - Keinänen - Psychosis metabolic risk calculator PsyMetRiC in early psychosis External.pdf (1.383Mb)
Lataukset: 

WILEY
doi:10.1111/acps.13752
URI
https://doi.org/10.1111/acps.13752
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082791798
Tiivistelmä

Introduction

Accurate detection of cardiometabolic risk in early psychosis is crucial to reducing somatic morbidity and mortality in people with psychotic disorders. We conducted an external validation of the psychosis metabolic risk calculator (PsyMetRiC), a cardiometabolic risk prediction tool developed in the UK and tailored for young people with psychosis. We compared the predictive accuracy and clinical usefulness of PsyMetRiC and a general population-based risk prediction tool for type 2 diabetes, the Finnish Diabetes Risk Score (FINDRISC).

Methods

We included first-episode psychosis and ultra-high-risk for psychosis patients without metabolic syndrome aged 18-35 years from the Helsinki Early Psychosis and Turku Early Psychosis Study cohorts. We tested two versions of PsyMetRiC: the full model including age, sex, ethnicity, body-mass index, smoking status, prescription of metabolically-active antipsychotic medication, high-density lipoprotein, and triglyceride concentrations, and the partial-model excluding biochemical predictors, and the simplified FINDRISC including BMI, sex, systolic blood pressure, and fasting glucose. Discrimination, calibration, and decision curve analyses were used to assess the predictive performance and clinical usefulness of both PsyMetRiC and FINDRISC. We performed a site-specific re-calibration of PsyMetRiC (PsyMetRiC-Fi).

Results

The study sample consisted of 278 individuals (all White European ethnicity, 58.6% male, mean age 24.8 years, 37.8% smoking, mean BMI 23.5). Discrimination was marginally better in the PsyMetRiC full model (C = 0.72, 95% CI, 0.59-0.82) compared with partial model (C = 0.70, 95% CI 0.59-0.80) or FINDRISC (C = 0.63, 95% CI 0.54-0.71). Calibration plots displayed evidence of minor miscalibration for PsyMetRiC, which corrected following recalibration. Miscalibration was more pronounced for FINDRISC. Decision curve analysis showed that PsyMetRiC offers likely clinical usefulness in improving cardiometabolic risk management in early psychosis compared with giving everyone or no one an intervention.

Conclusion

PsyMetRiC has utility in predicting cardiometabolic risk in Finnish patients with early psychosis. It has better discriminatory accuracy and offers more accurate risk prediction compared to other available strategies.

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