4.6 Article

Performance of the UK Prospective Diabetes Study Outcomes Model 2 in a Contemporary UK Type 2 Diabetes Trial Cohort

Journal

VALUE IN HEALTH
Volume 25, Issue 3, Pages 435-442

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jval.2021.09.005

Keywords

ASCEND; type 2 diabetes; UK Prospective Diabetes Study outcomes model; validation

Funding

  1. British Heart Foundation Centre of Research Excellence, Oxford, England, United Kingdom [RE/13/1/30181]

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By using data from ASCEND, the study assessed the performance of the UKPDS-OM2 model in predicting cardiovascular events and death risks in patients with T2D. The findings showed that the model substantially overpredicted risks of myocardial infarction, stroke, cardiovascular death, and other death, indicating the need for appropriate adjustments or a new model for accurate assessments in contemporary T2D cohorts.
Objectives: The UK Prospective Diabetes Study (UKPDS) Outcomes Model (UKPDS-OM) developed using 30-year (1977-2007) data from the UKPDS is widely used for health outcomes' projections and economic evaluations of therapies for patients with type 2 diabetes (T2D). Nevertheless, its reliability for contemporary UK T2D populations is unclear. We assessed the performance of version 2 of the model (UKPDS-OM2) using data from A Study of Cardiovascular Events in Diabetes (ASCEND), which followed participants with diabetes in the UK between 2005 and 2017.Methods: The UKPDS-OM2 was used to predict the occurrence of myocardial infarction (MI), other ischemic heart disease, stroke, cardiovascular (CV) death, and other death among the 14569 participants with T2D in ASCEND, all without previous CV disease at study entry. Calibration (comparison of predicted and observed year-on-year cumulative incidence over 10 years) and discrimination (c-statistics) of the model were assessed for each endpoint. The percentage error in event rates at year 7 (mean duration of follow up) was used to quantify model bias.Results: The UKPDS-OM2 substantially overpredicted MI, stroke, CV death, and other death over the 10-year follow-up period (by 149%, 42%, 269%, and 52%, respectively, at year 7). Discrimination of the model for MI and other ischemic heart disease (c-statistics 0.58 and 0.60, respectively) was poorer than that for other outcomes (c-statistics ranging from 0.66 to 0.72).Conclusions: The UKPDS-OM2 substantially overpredicted risks of key CV outcomes and death in people with T2D in ASCEND. Appropriate adjustments or a new model may be required for assessments of long-term effects of treatments in contemporary T2D cohorts.

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