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Saemann, M; Cejka, D; Schmaldienst, S; Rosenkranz, AR; Mayer, G.
Value of SGLT-2 inhibitors in the treatment of chronic kidney disease Clinical and practical implications
WIEN KLIN WOCHENSCHR. 2022;
Doi: 10.1007/s00508-022-02096-x
Web of Science
PubMed
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- Co-Autor*innen der Med Uni Graz
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Rosenkranz Alexander
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- Abstract:
- Chronic kidney disease (CKD) drastically increases the risk for cardiovascular morbidity and mortality and its worldwide prevalence is still rising. Effective treatment slows CKD progression, prevents development of end-stage kidney disease and cardiovascular disease thereby prolonging survival of patients. Recently, several large-scale studies with sodium-glucose cotransport-2 inhibitors (SGLT-2i) have demonstrated profound nephroprotective and cardioprotective properties in patients with type 2 diabetes mellitus with both CKD and heart failure. Recently, the dapagliflozin and prevention of adverse outcomes in chronic kidney disease (DAPA-CKD) trial demonstrated that the selective SGLT-2i dapagliflozin reduced the hazard ratio for a composite renal and cardiovascular death endpoint in patients with CKD with or without type 2 diabetes. Furthermore, dapagliflozin exerted strong nephroprotection in CKD patients with diverse etiologies like IgA nephropathy. Furthermore, other promising CKD trials such as with empagliflozin are underway. Hence, individualized treatment with SGLT2i represents a promising therapeutic option for patients with both diabetic and non-diabetic CKD. Here we summarize the current knowledge on the treatment with SGLT-2i in CKD patients underscoring a strong rationale for SGLT2 inhibition to be incorporated into standard of care for most CKD patients also with non-diabetic kidney disease. Finally, we aim to translate the current evidence into recommendations for the clinical practice in the management of patients with CKD.
- Find related publications in this database (Keywords)
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Endstage-kidney disease
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Albuminuria
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Heart failure
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Nephroprotection
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Cardiorenal syndrome