Empagliflozin Improves Kidney Outcomes in Patients With or Without Heart Failure.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
06 2019
Historique:
entrez: 6 6 2019
pubmed: 6 6 2019
medline: 9 4 2020
Statut: ppublish

Résumé

Background In EMPA-REG OUTCOME (Empagliflozin Cardiovascular Outcome Event Trial in Type 2 Diabetes Mellitus Patients) empagliflozin significantly reduced the risk of cardiovascular and kidney outcomes in patients with type 2 diabetes mellitus and established cardiovascular disease. Post hoc, we evaluated empagliflozin on kidney outcomes in patients with or without heart failure (HF). Methods and Results Individuals were randomized to empagliflozin 10 mg, 25 mg, or placebo. Prespecified analyses by baseline HF status included risk of incident or worsening nephropathy and estimated glomerular filtration rate slope analyses. Cox proportional hazards models assessed consistency of treatment effect across subgroups. Safety evaluations included kidney-related adverse events. At baseline, 244 (10.5%) and 462 (9.9%) patients had HF in the placebo and empagliflozin groups, respectively. Overall, the incidence of kidney outcome events was numerically higher in patients with than without HF. In the HF group, empagliflozin reduced risk of incident or worsening nephropathy or cardiovascular death by 43% (hazard ratio, 0.57 [95% CI, 0.42-0.77]) and progression to macroalbuminuria by 50% (hazard ratio, 0.50 [0.33-0.75]). After an initial transient decrease, estimated glomerular filtration rate stabilized over time with empagliflozin but gradually declined with placebo. Kidney effects in patients with HF were consistent with those in the overall study population (all P values for interaction >0.05). Across groups, the incidence rate of kidney-related adverse events/100 patient-years was higher in patients with than without HF; however, overall rates were comparable between groups. Conclusions These findings from EMPA-REG OUTCOME support the hypothesis that empagliflozin could reduce the risk of clinically relevant kidney events and may slow progression of chronic kidney disease in individuals with type 2 diabetes mellitus regardless of HF status. Clinical Trial Registration URL: https://www.clinicaltrials.gov . Unique identifier: NCT01131676.

Identifiants

pubmed: 31163986
doi: 10.1161/CIRCHEARTFAILURE.118.005875
doi:

Substances chimiques

Benzhydryl Compounds 0
Glucosides 0
Hypoglycemic Agents 0
Sodium-Glucose Transporter 2 Inhibitors 0
empagliflozin HDC1R2M35U

Banques de données

ClinicalTrials.gov
['NCT01131676']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e005875

Subventions

Organisme : NIGMS NIH HHS
ID : U54 GM115428
Pays : United States

Auteurs

Javed Butler (J)

Department of Medicine, University of Mississippi Medical Center, Jackson (J.B.).

Faiez Zannad (F)

Institut Lorrain du Coeur et des Vaisseaux, Nancy, France (F.Z.).

David Fitchett (D)

Division of Cardiology, St Michael's Hospital (D.F.), University of Toronto, Canada.

Bernard Zinman (B)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital (B.Z.), University of Toronto, Canada.

Audrey Koitka-Weber (A)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (A.K.-W., M.v.E., J.G., M.B.).
Department of Diabetes, Central Clinical School, Monash University, Melbourne, Australia (A.K.-W.).
Department of Medicine, Würzburg University Clinic, Germany (A.K.-W., C.W.).

Maximilian von Eynatten (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (A.K.-W., M.v.E., J.G., M.B.).

Isabella Zwiener (I)

Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany (I.Z.).

Jyothis George (J)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (A.K.-W., M.v.E., J.G., M.B.).

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (A.K.-W., M.v.E., J.G., M.B.).
Faculty of Medicine, University of Heidelberg, Mannheim, Germany (M.B.).

Alfred K Cheung (AK)

Division of Nephrology & Hypertension, University of Utah, Salt Lake City (A.K.C.).

Christoph Wanner (C)

Department of Medicine, Würzburg University Clinic, Germany (A.K.-W., C.W.).

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Classifications MeSH