The Present and Future
JACC State-of-the-Art Review
Clinical Benefit of Cardiorenal Effects of Sodium-Glucose Cotransporter 2 Inhibitors: JACC State-of-the-Art Review

https://doi.org/10.1016/j.jacc.2019.11.036Get rights and content
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Highlights

  • Patients with T2DM are at high risk of major vascular complications, HF, and chronic kidney disease.

  • SGLT2i reduce MACE and progression of chronic kidney disease in patients with T2DM.

  • SGLT2i also reduce HF and cardiovascular death in patients with established HF and reduced ejection fraction.

  • Ongoing trials are addressing the role of SGLT2i in patients with HF and preserved ejection fraction and chronic kidney disease, with and without T2DM.

Abstract

Changes in the regulatory guidelines by the U.S. Food and Drug Administration and the European Medical Agency requiring large-scale trials that study the cardiovascular safety of new glucose-lowering drugs have improved our understanding of type 2 diabetes mellitus. Unexpectedly, these trials demonstrated that sodium-glucose cotransporter 2 inhibitors reduce adverse cardiovascular outcomes. This second part of this 2-part review summarizes the findings of recent clinical trials and their clinical implications and describes ongoing trials and future areas of research.

Key Words

cardiorenal interaction
diabetes
heart failure
renal function
sodium-glucose cotransporter 2 inhibitor

Abbreviations and Acronyms

CI
confidence interval
eGFR
estimated glomerular filtration rate
HbA1c
glycosylated hemoglobin
HF
heart failure
HFpEF
heart failure with preserved ejection fraction
HFrEF
heart failure with reduced ejection fraction
HR
hazard ratio
MACE
major adverse cardiovascular events
SGLT2i
sodium-glucose cotransporter 2 inhibitor
T1DM
type 1 diabetes mellitus
T2DM
type 2 diabetes mellitus
UACR
urinary albumin-to-creatinine ratio

Cited by (0)

Dr. Zelniker is currently affiliated with the Division of Cardiology, Vienna General Hospital, Medical University of Vienna, Vienna, Austria. Dr. Zelniker has received grant support from the German Research Foundation (Deutsche Forschungsgemeinschaft ZE 1109/1-1); and has received lecture fees from AstraZeneca. Dr. Braunwald has received research grants through his institution from AstraZeneca, Daiichi-Sankyo, GlaxoSmithKline, Merck, and Novartis; has consultancies with Amgen, Cardurion, MyoKardia, NovoNordisk, and Verve; has received personal fees for lectures from Medscape; and has performed uncompensated consultancies and lectures with Novartis and The Medicines Company.

Listen to this manuscript's audio summary by Editor-in-Chief Dr. Valentin Fuster on JACC.org.