Background Inhibitors of sodium-glucose cotransporters type 2 (SGLT-2) are a class of oral antidiabetic drugs with a novel specific mode of action in the kidneys. Objective The effects of SGLT-2 inhibitors on cardiovascular (CV) and renal endpoints in outcome trials with type 2 diabetes patients. Material and methods Differential analysis and interpretation of the results of outcome trials with the SGLT-2 inhibitors empagliflozin, canagliflozin and dapagliflozin in type 2 diabetes mellitus. Results In the EMPA-REG OUTCOME trial, empagliflozin demonstrated a significant reduction in major cardiac adverse events (MACE), hospitalization for heart failure (HHI), renal endpoints, CV and total mortality vs. placebo in >7000 patients with type 2 diabetes and established CV disease over 3.1 years. In the CANVAS program, canagliflozin demonstrated a significant reduction of MACE, HHI and renal endpoints vs. placebo in >10,000 patients with type 2 diabetes and high CV risk over 2.4 years. In the CREDENCE trial, canagliflozin demonstrated a significant reduction of a combined renal endpoint and CV endpoints vs. placebo in >4000 patients with type 2 diabetes and established kidney disease with albuminuria over 2.6 years. In the DECLARE-TIMI 58 trial, dapagliflozin demonstrated a significant reduction in a combined endpoint of CV death and HHI vs. placebo in >17,000 patients with type 2 diabetes and established CV disease or with multiple CV risk factors over 3.1 years. Conclusion Outcome trials with SGLT-2 inhibitors have collectively demonstrated cardioprotective and nephroprotective effects in patients with type 2 diabetes and high CV risk. The use of SGLT-2 inhibitors is recommended in current guidelines and consensus statements as primary combination partners for metformin in patients with type 2 diabetes and established CV disease, high CV risk, heart failure or kidney disease.
机构:
Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USABrigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USA
Zelniker, Thomas A.
Wiviott, Stephen D.
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Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USABrigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USA
Wiviott, Stephen D.
Raz, Itamar
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Hadassah Med Ctr, Dept Endocrinol & Metab, Diabet Unit, Jerusalem, IsraelBrigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USA
Raz, Itamar
Sabatine, Marc S.
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Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USABrigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, Boston, MA 02115 USA
机构:
Università di Pisa,Dipartimento di Medicina Clinica e SperimentaleUniversità di Pisa,Dipartimento di Medicina Clinica e Sperimentale
Martina Chiriacò
Kyriazoula Chatzianagnostou
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Fondazione CNR Regione Toscana G. Monasterio,Centro di Ricerca Interdisciplinare “Health Science”Università di Pisa,Dipartimento di Medicina Clinica e Sperimentale
Kyriazoula Chatzianagnostou
Michele Emdin
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Fondazione CNR Regione Toscana G. Monasterio,Centro di Ricerca Interdisciplinare “Health Science”Università di Pisa,Dipartimento di Medicina Clinica e Sperimentale
Michele Emdin
Stefano Del Prato
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Scuola Superiore Sant’Anna,undefinedUniversità di Pisa,Dipartimento di Medicina Clinica e Sperimentale