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SGLT2 Inhibitors and the Risk of Venous Thromboembolism: A Population-based Cohort Study.

AIM The cardiovascular benefits of sodium glucose co-transporter 2 inhibitors (SGLT2Is) result from their complex impact on coronary and arterial vessels. However, their effect on veins and the risk of… Click to show full abstract

AIM The cardiovascular benefits of sodium glucose co-transporter 2 inhibitors (SGLT2Is) result from their complex impact on coronary and arterial vessels. However, their effect on veins and the risk of venous thromboembolism (VTE) remains unclear. Meta-analysis of trials has suggested no significant change in risk, but observational studies on the topic are scarce. Our objective was to determine if the use of SGLT2Is, compared to the use of dipeptidyl peptidase 4 inhibitors (DPP-4Is), is associated with the risk of VTE among patients with type 2 diabetes (T2DM). METHODS Using the Clinical Practice Research Datalink linked to hospitalization and vital statistics databases, we conducted a retrospective cohort study using a prevalent new-user design. SGLT2Is were matched to DPP-4I users on calendar time, diabetes treatment intensity, duration of previous DPP-4I use, and time-conditional high-dimensional propensity score. Cox proportional hazard models estimated the hazard ratio (HR) for VTE with SGLT2Is vs DPP-4Is. RESULTS SGLT2I use was not associated with an increased risk of VTE (HR: 0.65, 95% CI: 0.34 to 1.25). This finding was consistent among prevalent (HR: 0.47, 95% CI: 0.16 to 1.42) and incident new users (HR: 0.75, 95 % CI: 0.33 to 1.72). CONCLUSIONS We found that SGLT2Is were not associated with an increased risk of VTE compared to DPP-4Is. Although we observed a numerically decreased risk of VTE with SGLT2Is, estimates were accompanied by wide 95% CIs. Nonetheless, given the morbidity associated with VTE, our results provide some reassurance regarding the safety of SGLT2Is with respect to VTE.

Keywords: sglt2is; venous thromboembolism; vte; risk; risk vte; risk venous

Journal Title: British journal of clinical pharmacology
Year Published: 2023

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