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    The metabolic syndrome and cancer: Is the metabolic syndrome useful for predicting cancer risk above and beyond its individual components?

    Access Status
    Fulltext not available
    Authors
    Harding, J.
    Sooriyakumaran, M.
    Anstey, K.
    Adams, R.
    Balkau, B.
    Briffa, T.
    Davis, T.
    Davis, W.
    Dobson, A.
    Giles, G.
    Grant, J.
    Knuiman, M.
    Luszcz, M.
    Mitchell, P.
    Pasco, J.
    Reid, Christopher
    Simmons, D.
    Simons, L.
    Tonkin, A.
    Woodward, M.
    Shaw, J.
    Magliano, D.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Harding, J. and Sooriyakumaran, M. and Anstey, K. and Adams, R. and Balkau, B. and Briffa, T. and Davis, T. et al. 2015. The metabolic syndrome and cancer: Is the metabolic syndrome useful for predicting cancer risk above and beyond its individual components? Diabetes and Metabolism. 41 (6): pp. 463-469.
    Source Title
    Diabetes and Metabolism
    DOI
    10.1016/j.diabet.2015.04.006
    ISSN
    1262-3636
    School
    Department of Health Policy and Management
    URI
    http://hdl.handle.net/20.500.11937/27405
    Collection
    • Curtin Research Publications
    Abstract

    © 2015 Elsevier Masson SAS. Aims: The metabolic syndrome (MetS) is a risk factor for cancer. However, it is not known if the MetS confers a greater cancer risk than the sum of its individual components, which components drive the association, or if the MetS predicts future cancer risk. Materials and methods: We linked 20,648 participants from the Australian and New Zealand Diabetes and Cancer Collaboration with complete data on the MetS to national cancer registries and used Cox proportional hazards models to estimate associations of the MetS, the number of positive MetS components, and each of the five MetS components separately with the risk for overall, colorectal, prostate and breast cancer. Hazard ratios (HR) and 95% confidence intervals (95%CI) are reported. We assessed predictive ability of the MetS using Harrell's c-statistic. Results: The MetS was inversely associated with prostate cancer (HR 0.85; 95% CI 0.72-0.99). We found no evidence of an association between the MetS overall, colorectal and breast cancers. For those with five positive MetS components the HR was 1.12 (1.02-1.48) and 2.07 (1.26-3.39) for overall, and colorectal cancer, respectively, compared with those with zero positive MetS components. Greater waist circumference (WC) (1.38; 1.13-1.70) and elevated blood pressure (1.29; 1.01-1.64) were associated with colorectal cancer. Elevated WC and triglycerides were (inversely) associated with prostate cancer. MetS models were only poor to moderate discriminators for all cancer outcomes. Conclusions: We show that the MetS is (inversely) associated with prostate cancer, but is not associated with overall, colorectal or breast cancer. Although, persons with five positive components of the MetS are at a 1.2 and 2.1 increased risk for overall and colorectal cancer, respectively, and these associations appear to be driven, largely, by elevated WC and BP. We also demonstrate that the MetS is only a moderate discriminator of cancer risk.

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