SGLT2 Inhibition for CKD and Cardiovascular Disease in Type 2 Diabetes: Report of a Scientific Workshop Sponsored by the National Kidney Foundation

Author:

Tuttle Katherine R.1,Brosius Frank C.2ORCID,Cavender Matthew A.3,Fioretto Paola4,Fowler Kevin J.5,Heerspink Hiddo J.L.6,Manley Tom7,McGuire Darren K.8,Molitch Mark E.9,Mottl Amy K.3,Perreault Leigh10,Rosas Sylvia E.11,Rossing Peter1213,Sola Laura14,Vallon Volker15,Wanner Christoph16,Perkovic Vlado17

Affiliation:

1. Providence Health Care and University of Washington School of Medicine, Spokane, WA

2. University of Arizona College of Medicine, Tucson, AZ

3. University of North Carolina School of Medicine, Chapel Hill, NC

4. Department of Medicine, University of Padua, Padua, Italy

5. The Voice of the Patient, Inc, Elmhurst, IL

6. University of Groningen, Groningen, the Netherlands

7. National Kidney Foundation, New York, NY

8. University of Texas Southwestern Medical Center, Dallas, TX

9. Division of Endocrinology, Metabolism and Molecular Medicine, Northwestern, University Feinberg School of Medicine, Chicago, IL

10. University of Colorado Anschutz Medical Campus, Aurora, CO

11. Joslin Diabetes Center and Harvard Medical School, Boston, MA

12. Steno Diabetes Center Copenhagen, Gentofte, Denmark

13. University of Copenhagen, Copenhagen, Denmark

14. University of the Republic, Montevideo, Uruguay

15. University of California-San Diego, La Jolla, CA

16. Division of Nephrology, University Hospital Würzburg, Würzburg, Germany

17. George Institute for Global Health, UNSW Sydney, Australia

Abstract

Diabetes is the most frequent cause of chronic kidney disease (CKD), leading to nearly half of all cases of kidney failure requiring replacement therapy. The principal cause of death among patients with diabetes and CKD is cardiovascular disease (CVD). Sodium/glucose cotransporter 2 (SGLT2) inhibitors were developed to lower blood glucose levels by inhibiting glucose reabsorption in the proximal tubule. In clinical trials designed to demonstrate the CVD safety of SGLT2 inhibitors in type 2 diabetes mellitus (T2DM), consistent reductions in risks for secondary kidney disease end points (albuminuria and a composite of serum creatinine doubling or 40% estimated glomerular filtration rate decline, kidney failure, or death), along with reductions in CVD events, were observed. In patients with CKD, the kidney and CVD benefits of canagliflozin were established by the CREDENCE (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation) trial in patients with T2DM, urinary albumin-creatinine ratio >300 mg/g, and estimated glomerular filtration rate of 30 to <90 mL/min/1.73 m2. To clarify and support the role of SGLT2 inhibitors for treatment of T2DM and CKD, the National Kidney Foundation convened a scientific workshop with an international panel of more than 80 experts. They discussed the current state of knowledge and unanswered questions in order to propose therapeutic approaches and delineate future research. SGLT2 inhibitors improve glomerular hemodynamic function and are thought to ameliorate other local and systemic mechanisms involved in the pathogenesis of CKD and CVD. SGLT2 inhibitors should be used when possible by people with T2DM to reduce risks for CKD and CVD in alignment with the clinical trial entry criteria. Important risks of SGLT2 inhibitors include euglycemic ketoacidosis, genital mycotic infections, and volume depletion. Careful consideration should be given to the balance of benefits and harms of SGLT2 inhibitors and risk mitigation strategies. Effective implementation strategies are needed to achieve widespread use of these life-saving medications.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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