4.4 Article

Statin use and risk of developing diabetes: results from the Diabetes Prevention Program

Journal

BMJ OPEN DIABETES RESEARCH & CARE
Volume 5, Issue 1, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjdrc-2017-000438

Keywords

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Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health [U01 DK048489]
  2. NIDDK
  3. Intramural Research Program
  4. Indian Health Service
  5. National Institute of Child Health and Human Development
  6. National Institute on Aging
  7. National Eye Institute
  8. National Heart Lung and Blood Institute
  9. Office of Research on Women's Health
  10. National Institute on Minority Health and Health Disparities
  11. Centers for Disease Control and Prevention
  12. American Diabetes Association
  13. Bristol-Myers Squibb
  14. Parke-Davis
  15. McKesson BioServices
  16. Matthews Media Group
  17. Henry M Jackson Foundation

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Objective Several clinical trials of cardiovascular disease prevention with statins have reported increased risk of type 2 diabetes (T2DM) with statin therapy. However, participants in these studies were at relatively low risk for diabetes. Further, diabetes was often based on selfreport and was not the primary outcome. It is unknown whether statins similarly modify diabetes risk in higher risk populations. Research design and methods During the Diabetes Prevention Program Outcomes Study (n=3234), the long-term follow-up to a randomized clinical trial of interventions to prevent T2DM, incident diabetes was assessed by annual 75 g oral glucose tolerance testing and semiannual fasting glucose. Lipid profile was measured annually, with statin treatment determined by a participant's own physician outside of the protocol. Statin use was assessed at baseline and semiannual visits. Results At 10 years, the cumulative incidence of statin initiation prior to diabetes diagnosis was 33%-37% among the randomized treatment groups (p=0.36). Statin use was associated with greater diabetes risk irrespective of treatment group, with pooled HR (95% CI) for incident diabetes of 1.36 (1.17 to 1.58). This risk was not materially altered by adjustment for baseline diabetes risk factors and potential confounders related to indications for statin therapy. Conclusions In this population at high risk for diabetes, we observed significantly higher rates of diabetes with statin therapy in all three treatment groups. Confounding by indication for statin use does not appear to explain this relationship. The effect of statins to increase diabetes risk appears to extend to populations at high risk for diabetes.

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