Effect of Empagliflozin on Cardiovascular and Renal Outcomes in Patients With Heart Failure by Baseline Diabetes Status: Results From the EMPEROR-Reduced Trial.
Aged
Benzhydryl Compounds
/ pharmacology
Cardiovascular Diseases
/ drug therapy
Diabetes Mellitus, Type 2
/ drug therapy
Female
Glucosides
/ pharmacology
Heart Failure
/ complications
Humans
Male
Renal Insufficiency, Chronic
/ drug therapy
Sodium-Glucose Transporter 2 Inhibitors
/ pharmacology
Treatment Outcome
diabetes mellitus
empagliflozin
heart failure
Journal
Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763
Informations de publication
Date de publication:
26 01 2021
26 01 2021
Historique:
pubmed:
12
11
2020
medline:
29
12
2021
entrez:
11
11
2020
Statut:
ppublish
Résumé
Sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with heart failure with reduced ejection fraction, but additional information is needed about whether glycemic status influences the magnitude of their benefits on heart failure and renal events. Patients with Class II-IV heart failure and a left ventricular ejection fraction ≤40% were randomized to receive empagliflozin (10 mg daily) or placebo in addition to recommended therapy. We prespecified a comparison of the effect of empagliflozin in patients with and without diabetes. Of the 3730 patients enrolled, 1856 (50%) had diabetes, 1268 (34%) had prediabetes (hemoglobin A1c [HbA1c] 5.7-6.4%), and 606 (16%) had normoglycemia (HbA1c <5.7%). The risks of the primary outcome (cardiovascular death or hospitalization for heart failure), total hospitalizations for heart failure, and adverse renal outcomes were higher in patients with diabetes, but were similar between patients with prediabetes and normoglycemia. Empagliflozin reduced the risk of the primary outcome in patients with and without diabetes (hazard ratio, 0.72 [95% CI, 0.60-0.87] and 0.78 [95% CI, 0.64-0.97], respectively, In EMPEROR-Reduced (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Reduced Ejection Fraction), empagliflozin significantly improved cardiovascular and renal outcomes in patients with heart failure and a reduced ejection fraction, independent of baseline diabetes status and across the continuum of HbA1c. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03057977.
Sections du résumé
BACKGROUND
Sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with heart failure with reduced ejection fraction, but additional information is needed about whether glycemic status influences the magnitude of their benefits on heart failure and renal events.
METHODS
Patients with Class II-IV heart failure and a left ventricular ejection fraction ≤40% were randomized to receive empagliflozin (10 mg daily) or placebo in addition to recommended therapy. We prespecified a comparison of the effect of empagliflozin in patients with and without diabetes.
RESULTS
Of the 3730 patients enrolled, 1856 (50%) had diabetes, 1268 (34%) had prediabetes (hemoglobin A1c [HbA1c] 5.7-6.4%), and 606 (16%) had normoglycemia (HbA1c <5.7%). The risks of the primary outcome (cardiovascular death or hospitalization for heart failure), total hospitalizations for heart failure, and adverse renal outcomes were higher in patients with diabetes, but were similar between patients with prediabetes and normoglycemia. Empagliflozin reduced the risk of the primary outcome in patients with and without diabetes (hazard ratio, 0.72 [95% CI, 0.60-0.87] and 0.78 [95% CI, 0.64-0.97], respectively,
CONCLUSIONS
In EMPEROR-Reduced (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Reduced Ejection Fraction), empagliflozin significantly improved cardiovascular and renal outcomes in patients with heart failure and a reduced ejection fraction, independent of baseline diabetes status and across the continuum of HbA1c. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03057977.
Identifiants
pubmed: 33175585
doi: 10.1161/CIRCULATIONAHA.120.051824
pmc: PMC7834911
doi:
Substances chimiques
Benzhydryl Compounds
0
Glucosides
0
Sodium-Glucose Transporter 2 Inhibitors
0
empagliflozin
HDC1R2M35U
Banques de données
ClinicalTrials.gov
['NCT03057977']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
337-349Commentaires et corrections
Type : CommentIn
Références
Lancet. 2019 Jan 5;393(10166):31-39
pubmed: 30424892
Diabetes Care. 2020 Mar;43(3):508-511
pubmed: 32079684
BMJ Open Diabetes Res Care. 2020 May;8(1):
pubmed: 32457053
Lancet Diabetes Endocrinol. 2019 Nov;7(11):845-854
pubmed: 31495651
N Engl J Med. 2020 Oct 8;383(15):1413-1424
pubmed: 32865377
JAMA. 2020 Apr 14;323(14):1353-1368
pubmed: 32219386
Circ Heart Fail. 2016 Jan;9(1):
pubmed: 26754626
Eur J Heart Fail. 2019 Oct;21(10):1270-1278
pubmed: 31584231
Cardiovasc Diabetol. 2019 Aug 7;18(1):100
pubmed: 31391045
Eur J Heart Fail. 2011 Feb;13(2):195-9
pubmed: 21098576
Am J Hypertens. 2019 Nov 15;32(12):1170-1177
pubmed: 31257407
Eur J Heart Fail. 2020 Apr;22(4):604-617
pubmed: 31926059
N Engl J Med. 2019 Nov 21;381(21):1995-2008
pubmed: 31535829
Cardiovasc Drugs Ther. 2017 Dec;31(5-6):545-549
pubmed: 28948430
J Am Coll Cardiol. 2008 Jan 15;51(2):93-102
pubmed: 18191731