Effect of Empagliflozin on Left Ventricular Volumes in Patients With Type 2 Diabetes, or Prediabetes, and Heart Failure With Reduced Ejection Fraction (SUGAR-DM-HF).
Aged
Benzhydryl Compounds
/ pharmacology
Diabetes Mellitus, Type 2
/ drug therapy
Double-Blind Method
Female
Glucosides
/ pharmacology
Heart Failure
/ drug therapy
Humans
Male
Prediabetic State
/ drug therapy
Sodium-Glucose Transporter 2 Inhibitors
/ pharmacology
Stroke Volume
/ drug effects
Ventricular Remodeling
clinical trial
diabetes mellitus
empagliflozin
heart failure
magnetic resonance imaging
myocardium
sodium-glucose transporter 2 inhibitors
ventricular remodeling
Journal
Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763
Informations de publication
Date de publication:
09 02 2021
09 02 2021
Historique:
pubmed:
14
11
2020
medline:
22
12
2021
entrez:
13
11
2020
Statut:
ppublish
Résumé
Sodium-glucose cotransporter 2 inhibitors reduce the risk of heart failure hospitalization and cardiovascular death in patients with heart failure and reduced ejection fraction (HFrEF). However, their effects on cardiac structure and function in HFrEF are uncertain. We designed a multicenter, randomized, double-blind, placebo-controlled trial (the SUGAR-DM-HF trial [Studies of Empagliflozin and Its Cardiovascular, Renal and Metabolic Effects in Patients With Diabetes Mellitus, or Prediabetes, and Heart Failure]) to investigate the cardiac effects of empagliflozin in patients in New York Heart Association functional class II to IV with a left ventricular (LV) ejection fraction ≤40% and type 2 diabetes or prediabetes. Patients were randomly assigned 1:1 to empagliflozin 10 mg once daily or placebo, stratified by age (<65 and ≥65 years) and glycemic status (diabetes or prediabetes). The coprimary outcomes were change from baseline to 36 weeks in LV end-systolic volume indexed to body surface area and LV global longitudinal strain both measured using cardiovascular magnetic resonance. Secondary efficacy outcomes included other cardiovascular magnetic resonance measures (LV end-diastolic volume index, LV ejection fraction), diuretic intensification, symptoms (Kansas City Cardiomyopathy Questionnaire Total Symptom Score, 6-minute walk distance, B-lines on lung ultrasound, and biomarkers (including N-terminal pro-B-type natriuretic peptide). From April 2018 to August 2019, 105 patients were randomly assigned: mean age 68.7 (SD, 11.1) years, 77 (73.3%) male, 82 (78.1%) diabetes and 23 (21.9%) prediabetes, mean LV ejection fraction 32.5% (9.8%), and 81 (77.1%) New York Heart Association II and 24 (22.9%) New York Heart Association III. Patients received standard treatment for HFrEF. In comparison with placebo, empagliflozin reduced LV end-systolic volume index by 6.0 (95% CI, -10.8 to -1.2) mL/m The sodium-glucose cotransporter 2 inhibitor empagliflozin reduced LV volumes in patients with HFrEF and type 2 diabetes or prediabetes. Favorable reverse LV remodeling may be a mechanism by which sodium-glucose cotransporter 2 inhibitors reduce heart failure hospitalization and mortality in HFrEF. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT03485092.
Sections du résumé
BACKGROUND
Sodium-glucose cotransporter 2 inhibitors reduce the risk of heart failure hospitalization and cardiovascular death in patients with heart failure and reduced ejection fraction (HFrEF). However, their effects on cardiac structure and function in HFrEF are uncertain.
METHODS
We designed a multicenter, randomized, double-blind, placebo-controlled trial (the SUGAR-DM-HF trial [Studies of Empagliflozin and Its Cardiovascular, Renal and Metabolic Effects in Patients With Diabetes Mellitus, or Prediabetes, and Heart Failure]) to investigate the cardiac effects of empagliflozin in patients in New York Heart Association functional class II to IV with a left ventricular (LV) ejection fraction ≤40% and type 2 diabetes or prediabetes. Patients were randomly assigned 1:1 to empagliflozin 10 mg once daily or placebo, stratified by age (<65 and ≥65 years) and glycemic status (diabetes or prediabetes). The coprimary outcomes were change from baseline to 36 weeks in LV end-systolic volume indexed to body surface area and LV global longitudinal strain both measured using cardiovascular magnetic resonance. Secondary efficacy outcomes included other cardiovascular magnetic resonance measures (LV end-diastolic volume index, LV ejection fraction), diuretic intensification, symptoms (Kansas City Cardiomyopathy Questionnaire Total Symptom Score, 6-minute walk distance, B-lines on lung ultrasound, and biomarkers (including N-terminal pro-B-type natriuretic peptide).
RESULTS
From April 2018 to August 2019, 105 patients were randomly assigned: mean age 68.7 (SD, 11.1) years, 77 (73.3%) male, 82 (78.1%) diabetes and 23 (21.9%) prediabetes, mean LV ejection fraction 32.5% (9.8%), and 81 (77.1%) New York Heart Association II and 24 (22.9%) New York Heart Association III. Patients received standard treatment for HFrEF. In comparison with placebo, empagliflozin reduced LV end-systolic volume index by 6.0 (95% CI, -10.8 to -1.2) mL/m
CONCLUSIONS
The sodium-glucose cotransporter 2 inhibitor empagliflozin reduced LV volumes in patients with HFrEF and type 2 diabetes or prediabetes. Favorable reverse LV remodeling may be a mechanism by which sodium-glucose cotransporter 2 inhibitors reduce heart failure hospitalization and mortality in HFrEF. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT03485092.
Identifiants
pubmed: 33186500
doi: 10.1161/CIRCULATIONAHA.120.052186
pmc: PMC7864599
doi:
Substances chimiques
Benzhydryl Compounds
0
Glucosides
0
Sodium-Glucose Transporter 2 Inhibitors
0
empagliflozin
HDC1R2M35U
Banques de données
ClinicalTrials.gov
['NCT03485092']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
516-525Subventions
Organisme : Medical Research Council
ID : MR/P023398/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N003403/1
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/15/54/31639
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/17/25/32884
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/17/26/32744
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S005714/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P023398/1
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Références
J Cardiovasc Imaging. 2020 Apr;28(2):137-149
pubmed: 32233166
N Engl J Med. 2020 Oct 8;383(15):1413-1424
pubmed: 32865377
J Cardiovasc Magn Reson. 2016 Nov 30;18(1):89
pubmed: 27899132
Hypertension. 2013 Apr;61(4):770-8
pubmed: 23424238
Circ Heart Fail. 2020 Sep;13(9):e007197
pubmed: 32894987
J Am Coll Cardiol. 2000 Mar 1;35(3):569-82
pubmed: 10716457
J Am Coll Cardiol. 2000 Dec;36(7):2072-80
pubmed: 11127443
JACC Heart Fail. 2019 Oct;7(10):849-858
pubmed: 31582107
Eur Heart J. 2011 Oct;32(20):2507-15
pubmed: 21875858
Sci Rep. 2020 Feb 27;10(1):3582
pubmed: 32107428
Heart. 2004 Jul;90(7):760-4
pubmed: 15201244
J Am Coll Cardiol. 2002 Sep 4;40(5):970-5
pubmed: 12225725
Circulation. 2019 Mar 12;139(11):1354-1365
pubmed: 30586756
JACC Cardiovasc Imaging. 2011 Jan;4(1):98-108
pubmed: 21232712
J Cardiovasc Magn Reson. 2016 Apr 12;18:21
pubmed: 27071974
J Am Coll Cardiol. 2000 Apr;35(5):1245-55
pubmed: 10758967
J Cardiovasc Magn Reson. 2020 Jan 30;22(1):9
pubmed: 31996239
JACC Cardiovasc Imaging. 2018 Oct;11(10):1419-1429
pubmed: 29361479
JAMA. 2019 Sep 2;:1-10
pubmed: 31475296
Am Heart J. 1998 May;135(5 Pt 1):825-32
pubmed: 9588412
J Cardiovasc Magn Reson. 2017 Feb 3;19(1):18
pubmed: 28178995
Circulation. 2007 Jul 3;116(1):49-56
pubmed: 17576868
J Am Coll Cardiol. 2010 Jul 27;56(5):392-406
pubmed: 20650361
Am Heart J. 2001 Oct;142(4):698-703
pubmed: 11579362
Circulation. 1995 May 15;91(10):2573-81
pubmed: 7743619
N Engl J Med. 2005 Apr 14;352(15):1539-49
pubmed: 15753115
Circulation. 2019 Nov 19;140(21):1693-1702
pubmed: 31434508
N Engl J Med. 2019 Nov 21;381(21):1995-2008
pubmed: 31535829
J Cardiovasc Magn Reson. 2015 Jul 16;17:62
pubmed: 26174798
Diabetes Care. 2020 Jun;43(6):1356-1359
pubmed: 32245746
Hypertension. 2013 Apr;61(4):762-4
pubmed: 23424234