An association between anti-platelet drug use and reduced cancer prevalence in diabetic patients: Results from the Vermont Diabetes Information System Study

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Abstract

Background: Diabetes is associated with an increased risk of several malignancies. Both diabetic patients and patients with cancer have an increase in platelet reactivity and platelet activation has recently emerged as a potential mediator of cancer progression. Drug therapies, such as aspirin, that reduce platelet reactivity reduce both cardiovascular and cancer risk.Methods: We performed a cross-sectional analysis to assess the association between history of cancer and current anti-platelet drug use in a primary care population of adults with diabetes enrolled in the Vermont Diabetes Information System.Results: Self-reported characteristics, medical history, and a complete medication list were recorded on 1007 diabetic adults. Fifty percent of diabetic patients used an anti-platelet drug. In unadjusted analysis, no association was seen between anti-platelet drug use and cancer history (OR = 0.93; P = .70). Platelet inhibitor use was associated with a decreased patient-reported history of malignancy in a multivariate logistic regression adjusted for age, sex, body mass index, comorbidity, and number of medications (OR = 0.66; CI 0.44-0.99; P = .045). Similar odds of association were seen in both males and females, and for aspirin and non-aspirin platelet inhibitor therapy.Conclusions: Our data suggest an association between anti-platelet drug use and reduced cancer prevalence in patients with diabetes. Given the potentially large implications of our observations in the diabetic population, further studies are required to determine if this association is causal. © 2010 Holmes et al; licensee BioMed Central Ltd.

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Holmes, C. E., Ramos-Nino, M. E., & Littenberg, B. (2010). An association between anti-platelet drug use and reduced cancer prevalence in diabetic patients: Results from the Vermont Diabetes Information System Study. BMC Cancer, 10. https://doi.org/10.1186/1471-2407-10-289

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