Sodium-glucose cotransporter 2 inhibition: towards an indication to treat diabetic kidney disease

Author:

Górriz Jose Luis12ORCID,Navarro-González Juan F234,Ortiz Alberto25,Vergara Ander67,Nuñez Julio89,Jacobs-Cachá Conxita67,Martínez-Castelao Alberto210,Soler Maria Jose267ORCID

Affiliation:

1. Hospital Clínico Universitario de Valencia, Universitat de València, INCLIVA, GEENDIAB, Valencia, Spain

2. REDINREN, Madrid, Spain

3. Unidad de Investigación y Servicio de Nefrología, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain

4. Instituto de Tecnologías Biomédicas, Universidad de La Laguna, GEENDIAB, Santa Cruz de Tenerife, Spain

5. IIS-Fundación Jimenez Diaz UAM and School of Medicine, UAM, GEENDIAB, Madrid, Spain

6. Department of Nephrology, Hospital Universitari Vall d’Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain

7. Nephrology Research Group, Vall d’Hebron Research Institute (VHIR), GEENDIAB, Barcelona, Spain

8. Department of Cardiology, Hospital Clínico Universitario de Valencia, Universitat de Valencia, INCLIVA, Valencia, Spain

9. CIBER Cardiovascular

10. Bellvitge University Hospital, Hospitalet, GEENDIAB, Barcelona, Spain

Abstract

Abstract Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have clearly demonstrated their beneficial effect in diabetic kidney disease (DKD) on top of the standard of care [blood glucose control, renin–angiotensin system blockade, smoking cessation and blood pressure (BP) control], even in patients with overt DKD. However, the indication of this drug class is still blood glucose lowering in type 2 diabetic patients with estimated glomerular filtration rate >45 mL/min/1.73 m2. Based on the new evidence, several scientific societies have emphasized the preferential prescription of SGLT2i for patients at risk of heart failure or kidney disease, but still within the limits set by health authorities. A rapid positioning of both the European Medicines Agency and the US Food and Drug Administration will allow patients with overt DKD to benefit from SGLT2i. Clinical experience suggests that SGLT2i safety management may in part mirror renin–angiotensin blockade safety management in patients with overt DKD. This review focuses on the rationale for an indication of SGTL2i in DKD. We further propose clinical steps for maximizing the safety of SGLT2i in DKD patients on other antidiabetic, BP or diuretic medication.

Funder

FIS/Fondos FEDER

FRIAT

Sociedad Española de Nefrología, Comunidad de Madrid en Biomedicina

CIFRA2-CM

CIBER

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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