4.8 Article

Sodium Glucose Cotransporter-2 Inhibition in Heart Failure Potential Mechanisms, Clinical Applications, and Summary of Clinical Trials

期刊

CIRCULATION
卷 136, 期 17, 页码 1643-1658

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCULATIONAHA.117.030012

关键词

clinical trial; heart failure; sodium glucose transporter 2

资金

  1. Canadian Diabetes Association Fellowship
  2. Sunnybrook Health Sciences Center, University of Toronto
  3. NIH [T32-DK063687]
  4. Thrasher Foundation
  5. Juvenile Diabetes Research Foundation (JDRF)
  6. International Society of Pediatric and Adolescent Diabetes (ISPAD)
  7. Center for Women's Health Research at University of Colorado
  8. Heart and Stroke Foundation of Canada National New Investigator/Ontario Clinician Scientist Award
  9. Ontario Ministry of Research and Innovation Early Researcher Award
  10. Women's College Research Institute, Women's College Hospital
  11. Peter Munk Cardiac Center, University Health Network
  12. Department of Medicine and Heart and Stroke Richard Lewar Center of Excellence in Cardiovascular Research, University of Toronto
  13. Canadian Institutes of Health Research, and Diabetes Action Canada, a Strategy for Patient-Oriented Research
  14. Canadian Institutes for Health Research
  15. Heart and Stroke Richard Lewar Center of Excellence in Cardiovascular Research
  16. Banting and Best Diabetes Center, University of Toronto
  17. University of Toronto, Department of Medicine Merit Award
  18. Department of Medicine, Women's College Hospital

向作者/读者索取更多资源

Despite current established therapy, heart failure (HF) remains a leading cause of hospitalization and mortality worldwide. Novel therapeutic targets are therefore needed to improve the prognosis of patients with HF. The EMPA-REG OUTCOME trial ([Empagliflozin] Cardiovascular Outcome Event Trial in Type 2 Diabetes Mellitus Patients) demonstrated significant reductions in mortality and HF hospitalization risk in patients with type 2 diabetes mellitus (T2D) and cardiovascular disease with the antihyperglycemic agent, empagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor. The CANVAS trial (Canagliflozin Cardiovascular Assessment Study) subsequently reported a reduction in 3-point major adverse cardiovascular events and HF hospitalization risk. Although SGLT2 inhibition may have potential application beyond T2D, including HF, the mechanisms responsible for the cardioprotective effects of SGLT2 inhibitors remain incompletely understood. SGLT2 inhibition promotes natriuresis and osmotic diuresis, leading to plasma volume contraction and reduced preload, and decreases in blood pressure, arterial stiffness, and afterload as well, thereby improving subendocardial blood flow in patients with HF. SGLT2 inhibition is also associated with preservation of renal function. Based on data from mechanistic studies and clinical trials, large clinical trials with SGLT2 inhibitors are now investigating the potential use of SGLT2 inhibition in patients who have HF with and without T2D. Accordingly, in this review, we summarize the key pharmacodynamic effects of SGLT2 inhibitors and the clinical evidence that support the rationale for the use of SGLT2 inhibitors in patients with HF who have T2D. Because these favorable effects presumably occur independent of blood glucose lowering, we also explore the potential use of SGLT2 inhibition in patients without T2D with HF or at risk of HF, such as in patients with coronary artery disease or hypertension. Finally, we provide a detailed overview and summary of ongoing cardiovascular outcome trials with SGLT2 inhibitors.

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