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    Cardiovascular risk prediction in a population with the metabolic syndrome: Framingham vs. UKPDS algorithms

    Access Status
    Fulltext not available
    Authors
    Zomer, E.
    Liew, D.
    Owen, A.
    Magliano, D.
    Ademi, Z.
    Reid, Christopher
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Zomer, E. and Liew, D. and Owen, A. and Magliano, D. and Ademi, Z. and Reid, C. 2014. Cardiovascular risk prediction in a population with the metabolic syndrome: Framingham vs. UKPDS algorithms. European Journal of Preventive Cardiology. 21 (3): pp. 384-390.
    Source Title
    European Journal of Preventive Cardiology
    DOI
    10.1177/2047487312449307
    ISSN
    2047-4873
    School
    Department of Health Policy and Management
    URI
    http://hdl.handle.net/20.500.11937/23405
    Collection
    • Curtin Research Publications
    Abstract

    Background: Cardiovascular disease (CVD) risk-prediction algorithms are key in determining one’s eligibility for prevention strategies, but are often population-specific. Metabolic syndrome (MetS), a clustering of risk factors that increase the risk of CVD, does not currently have a risk-prediction algorithm available for prediction of CVD. The aim of this study was to compare the predictive capacities of an algorithm intended for ‘healthy’ individuals and one intended for ‘diabetic’ individuals. Methods: Individual-specific data from 2700 subjects defined as MetS but free of diagnosed CVD from the Australian Diabetes, Obesity and Lifestyle study was used to estimate 5-year risk of CVD using the two algorithms, and compared using Wilcoxon-signed rank test. CVD end point data was used to assess the performance using discrimination and calibration techniques of the two algorithms. Results: Five-year risk-prediction comparisons demonstrated that the UKPDS algorithm overpredicted risk in the younger age groups (25–54 years) and underpredicted risk in the older age groups (≥55 years) compared to the Framingham algorithm. A total of 133 CVD events occurred over a median follow up of 5.0 years. Model performance analyses demonstrated both the Framingham and UKPDS algorithms were poor at discrimination (area under receiver operator curve 0.513 and 0.524, respectively) and calibration (Hosmer-Lemeshow 467.1 and 297.0, respectively). Conclusions: Neither the Framingham or UKPDS algorithms are ideal for prediction of CVD risk in a MetS population. This study highlights the need for development of population-specific risk-prediction algorithms for this growing population group.

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