Empagliflozin Improves Kidney Outcomes in Patients With or Without Heart Failure.
Adult
Aged
Albuminuria
/ drug therapy
Benzhydryl Compounds
/ therapeutic use
Cardiovascular Diseases
/ complications
Diabetes Mellitus, Type 2
/ drug therapy
Female
Glomerular Filtration Rate
/ drug effects
Glucosides
/ therapeutic use
Heart Failure
/ drug therapy
Humans
Hypoglycemic Agents
/ therapeutic use
Kidney
/ drug effects
Male
Middle Aged
Risk Factors
Sodium-Glucose Transporter 2 Inhibitors
/ therapeutic use
cardiovascular diseases
chronic kidney disease
diabetes mellitus, type 2
heart failure
sodium-glucose transporter 2
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
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
e005875Subventions
Organisme : NIGMS NIH HHS
ID : U54 GM115428
Pays : United States