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Empagliflozin and Cardiovascular and Kidney Outcomes across KDIGO Risk Categories: Post Hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Multinational Trial.
- Source :
-
Clinical journal of the American Society of Nephrology : CJASN [Clin J Am Soc Nephrol] 2020 Oct 07; Vol. 15 (10), pp. 1433-1444. Date of Electronic Publication: 2020 Sep 29. - Publication Year :
- 2020
-
Abstract
- Background and Objectives: In the Empagliflozin Cardiovascular Outcome Event Trial in Type 2 Diabetes Mellitus Patients (EMPA-REG Outcome), empagliflozin, in addition to standard of care, significantly reduced risk of cardiovascular death by 38%, hospitalization for heart failure by 35%, and incident or worsening nephropathy by 39% compared with placebo in patients with type 2 diabetes and established cardiovascular disease. Using EMPA-REG Outcome data, we assessed whether the Kidney Disease Improving Global Outcomes (KDIGO) CKD classification had an influence on the treatment effect of empagliflozin.<br />Design, Setting, Participants, & Measurements: Patients with type 2 diabetes, established atherosclerotic cardiovascular disease, and eGFR≥30 ml/min per 1.73 m <superscript>2</superscript> at screening were randomized to receive empagliflozin 10 mg, empagliflozin 25 mg, or placebo once daily in addition to standard of care. Post hoc , we analyzed cardiovascular and kidney outcomes, and safety, using the two-dimensional KDIGO classification framework.<br />Results: Of 6952 patients with baseline eGFR and urinary albumin-creatinine ratio values, 47%, 29%, 15%, and 8% were classified into low, moderately increased, high, and very high KDIGO risk categories, respectively. Empagliflozin showed consistent risk reductions across KDIGO categories for cardiovascular outcomes ( P values for treatment by subgroup interactions ranged from 0.26 to 0.85) and kidney outcomes ( P values for treatment by subgroup interactions ranged from 0.16 to 0.60). In all KDIGO risk categories, placebo and empagliflozin had similar adverse event rates, the notable exception being genital infection events, which were more common with empagliflozin for each category.<br />Conclusions: The observed effects of empagliflozin versus placebo on cardiovascular and kidney outcomes were consistent across the KDIGO risk categories, indicating that the effect of treatment benefit of empagliflozin was unaffected by baseline CKD status.<br />Clinical Trial Registry Name and Registration Number: EMPA-REG OUTCOME, NCT01131676.<br /> (Copyright © 2020 by the American Society of Nephrology.)
- Subjects :
- Adams-Stokes Syndrome etiology
Aged
Albuminuria urine
Benzhydryl Compounds adverse effects
Creatinine urine
Diabetes Mellitus, Type 2 complications
Double-Blind Method
Female
Genital Diseases, Female chemically induced
Genital Diseases, Male chemically induced
Glomerular Filtration Rate
Glucosides adverse effects
Heart Failure etiology
Hospitalization
Humans
Infections chemically induced
Male
Middle Aged
Mortality
Myocardial Infarction etiology
Placebos
Renal Insufficiency, Chronic complications
Sodium-Glucose Transporter 2 Inhibitors adverse effects
Benzhydryl Compounds therapeutic use
Cardiovascular Diseases complications
Diabetes Mellitus, Type 2 drug therapy
Glucosides therapeutic use
Renal Insufficiency, Chronic classification
Renal Insufficiency, Chronic physiopathology
Sodium-Glucose Transporter 2 Inhibitors therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1555-905X
- Volume :
- 15
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Clinical journal of the American Society of Nephrology : CJASN
- Publication Type :
- Academic Journal
- Accession number :
- 32994159
- Full Text :
- https://doi.org/10.2215/CJN.14901219