Abstract
Hospitalization for major diabetes complications, including myocardial infarction, stroke, lower-extremity amputation, and end-stage kidney disease, is on the rise and represents a great health burden for patients with type 2 diabetes (T2D), in particular for older people. Newer glucose-lowering medications have generated some optimism on the possibility to influence the natural history of cardiorenal complications of T2D. This review summarizes work in the area of sodium-glucose cotransporter 2 inhibitors (SGLT-2i) treatment and prevention of cardiorenal complications in patients with T2D (major adverse cardiovascular events, hospitalization for heart failure, kidney outcomes), with a particular emphasis on the effect of age, the role of primary versus secondary prevention and the possible extension of their cardiorenal benefits to the entire class of SGLT-2i.
Keywords:
Age; Class effect; Diabetic kidney disease; Heart failure; MACE; Primary and secondary prevention; SGLT-2 inhibitors; Type 2 diabetes.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Biomarkers / blood
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Blood Glucose / drug effects*
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Blood Glucose / metabolism
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Diabetes Mellitus, Type 2 / blood
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Diabetes Mellitus, Type 2 / diagnosis
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Diabetes Mellitus, Type 2 / drug therapy*
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Diabetes Mellitus, Type 2 / epidemiology
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Diabetic Cardiomyopathies / diagnosis
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Diabetic Cardiomyopathies / epidemiology
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Diabetic Cardiomyopathies / prevention & control*
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Diabetic Nephropathies / diagnosis
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Diabetic Nephropathies / epidemiology
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Diabetic Nephropathies / prevention & control*
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Glycated Hemoglobin / metabolism
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Glycemic Control* / adverse effects
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Heart Failure / diagnosis
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Heart Failure / epidemiology
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Heart Failure / prevention & control*
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Humans
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Primary Prevention
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Risk Assessment
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Risk Factors
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Secondary Prevention
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Sodium-Glucose Transporter 2 Inhibitors / adverse effects
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Sodium-Glucose Transporter 2 Inhibitors / therapeutic use*
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Treatment Outcome
Substances
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Biomarkers
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Blood Glucose
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Glycated Hemoglobin A
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Sodium-Glucose Transporter 2 Inhibitors
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hemoglobin A1c protein, human