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Introduction 95% CI=1.01-1.11), driven by a 13% increase in risk of MI. Compared with SUs, DPP-4i had a 10% decrease in the risk of MACE. Conclusion: This study suggests robust reductions in rates of MACE with SGLT2i and GLP-1RA compared to DPP-4i or SUs in patients with T2D and no CV disease. Although differences were not large, the risk of MACE was lower with GLP-1RA (vs SGLT2i) and DPP-4i (vs SUs). Disclosure E. Patorno: Research Support; Boehringer-Ingelheim, Food and Drug Administration (FDA), National Institutes of Health, Patient-Centered Outcomes Research Institute. H. Tesfaye: None. C. Alix: None. E.C. DiCesare: None. S. Cromer: Other Relationship; Johnson Alexion Pharmaceuticals, Inc. Other Relationship; Wolters Kluwer Health. B.M. Everett: Consultant; Novo Nordisk. Research Support; Novo Nordisk. Consultant; Eli Lilly and Company, Janssen Pharmaceuticals, Inc., Ipsen Pharmaceuticals, Provention Bio, Inc. R. Glynn: Research Support; Amarin Corporation, Kowa Pharmaceuticals America, Inc., Novartis AG, Pfizer Inc. D.J. Wexler: Other Relationship; Novo Nordisk. J.M. Paik: None. Funding Patient Centered Outcomes Research Institute (DB-2020C2-20326)
PATORNO et al. (Fri,) studied this question.