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Midlife metabolic factors and prostate cancer risk in later life
Authors:Barbra A. Dickerman  Johanna E. Torfadottir  Unnur A. Valdimarsdottir  Kathryn M. Wilson  Laufey Steingrimsdottir  Thor Aspelund  Julie L. Batista  Katja Fall  Edward Giovannucci  Lara G. Sigurdardottir  Laufey Tryggvadottir  Vilmundur Gudnason  Lorelei A. Mucci
Affiliation:1. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA;2. Centre for Public Health Sciences, University of Iceland, Reykjavik, Iceland;3. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden;4. Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA;5. Unit for Nutrition Research, University Hospital & the Faculty of Food Science and Nutrition, University of Iceland, Reykjavik, Iceland;6. The Icelandic Heart Association, Kopavogur, Iceland;7. Clinical Epidemiology and Biostatistics, ?rebro University Hospital, ?rebro, Sweden;8. Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA;9. Faculty of Medicine, University of Iceland, Reykjavik, Iceland;10. Department of Education and Prevention, The Icelandic Cancer Society, Reykjavik, Iceland;11. The Icelandic Cancer Registry, Reykjavik, Iceland
Abstract:Metabolic syndrome is associated with several cancers, but evidence for aggressive prostate cancer is sparse. We prospectively investigated the influence of metabolic syndrome and its components on risk of total prostate cancer and measures of aggressive disease in a cohort of Icelandic men. Men in the Reykjavik Study (n = 9,097, enrolled 1967–1987) were followed for incident (n = 1,084 total; n = 378 advanced; n = 148 high‐grade) and fatal (n = 340) prostate cancer until 2014. Cox regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for (1) measured metabolic factors at cohort entry (body mass index (BMI), blood pressure, triglycerides, fasting blood glucose) and (2) a metabolic syndrome score (range 0–4) combining the risk factors: BMI ≥30 kg/m2; systolic blood pressure (SBP) ≥130 or diastolic blood pressure (DBP) ≥85 mm Hg or taking antihypertensives; triglycerides ≥150 mg/dl; fasting blood glucose ≥100 mg/dl or self‐reported type 2 diabetes. Hypertension and type 2 diabetes were associated with a higher risk of total, advanced, high‐grade, and fatal prostate cancer, independent of BMI. Neither BMI nor triglycerides were associated with prostate cancer risk. Higher metabolic syndrome score (3–4 vs 0) was associated with a higher risk of fatal prostate cancer (HR 1.55; 95% CI: 0.89, 2.69; p trend = 0.08), although this finding was not statistically significant. Our findings suggest a positive association between midlife hypertension and diabetes and risk of total and aggressive prostate cancer. Further, metabolic syndrome as a combination of factors was associated with an increased risk of fatal prostate cancer.
Keywords:prostate cancer  metabolic syndrome  BMI  hypertension  triglycerides  fasting blood glucose  diabetes
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