Nature Medicine, volume 27, issue 11, pages 1954-1960

The SGLT2 inhibitor dapagliflozin in heart failure with preserved ejection fraction: a multicenter randomized trial

Michael E. Nassif 1, 2
Sheryl L. Windsor 1
Barry A. Borlaug 3
Dalane W. Kitzman 4
S J Shah 5
Fengming Tang 1
Yevgeniy Khariton 1, 2
Ali O Malik 1, 2
Taiyeb Khumri 1
Guillermo Umpierrez 6
Sumant Lamba 7
Kavita Sharma 8
Sadiya S. Khan 5
Lokesh Chandra 9
Robert A. Gordon 10
John J. Ryan 11
Sunit-Preet Chaudhry 12
Susan M. Joseph 13
Chen H. Chow 14
Manreet K. Kanwar 15
Michael Pursley 16
Elias S. Siraj 17
Gregory D. Lewis 18
Barry S. Clemson 19
Michael W. Fong 20
Mikhail Kosiborod 1, 2, 21, 22
Show full list: 26 authors
1
 
Saint Luke’s Mid America Heart Institute, Kansas City, USA
7
 
First Coast Cardiovascular Institute, Jacksonville, USA
9
 
Chicago Medical Research, Hazel Crest, USA
10
 
Northshore University Healthsystem, Evanston, USA
12
 
Ascension St. Vincent, Indianapolis, USA
14
 
Stormont Vail Health, Topeka, USA
15
 
Cardiovascular Institute, Allegheny Health Network, Pittsburgh, USA
16
 
Heart Group of the Eastern Shore, Fairhope, USA
17
 
Eastern Virginia Medical School, Norfolk, USA
19
 
OSF HealthCare Cardiovascular Institute, Peoria, USA
Publication typeJournal Article
Publication date2021-10-28
Journal: Nature Medicine
scimago Q1
SJR19.045
CiteScore100.9
Impact factor58.7
ISSN10788956, 1546170X, 17447933
General Biochemistry, Genetics and Molecular Biology
General Medicine
Abstract
Patients with heart failure and preserved ejection fraction (HFpEF) have a high burden of symptoms and functional limitations, and have a poor quality of life. By targeting cardiometabolic abmormalities, sodium glucose cotransporter 2 (SGLT2) inhibitors may improve these impairments. In this multicenter, randomized trial of patients with HFpEF (NCT03030235), we evaluated whether the SGLT2 inhibitor dapagliflozin improves the primary endpoint of Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CS), a measure of heart failure-related health status, at 12 weeks after treatment initiation. Secondary endpoints included the 6-minute walk test (6MWT), KCCQ Overall Summary Score (KCCQ-OS), clinically meaningful changes in KCCQ-CS and -OS, and changes in weight, natriuretic peptides, glycated hemoglobin and systolic blood pressure. In total, 324 patients were randomized to dapagliflozin or placebo. Dapagliflozin improved KCCQ-CS (effect size, 5.8 points (95% confidence interval (CI) 2.3–9.2, P = 0.001), meeting the predefined primary endpoint, due to improvements in both KCCQ total symptom score (KCCQ-TS) (5.8 points (95% CI 2.0–9.6, P = 0.003)) and physical limitations scores (5.3 points (95% CI 0.7–10.0, P = 0.026)). Dapagliflozin also improved 6MWT (mean effect size of 20.1 m (95% CI 5.6–34.7, P = 0.007)), KCCQ-OS (4.5 points (95% CI 1.1–7.8, P = 0.009)), proportion of participants with 5-point or greater improvements in KCCQ-OS (odds ratio (OR) = 1.73 (95% CI 1.05–2.85, P = 0.03)) and reduced weight (mean effect size, 0.72 kg (95% CI 0.01–1.42, P = 0.046)). There were no significant differences in other secondary endpoints. Adverse events were similar between dapagliflozin and placebo (44 (27.2%) versus 38 (23.5%) patients, respectively). These results indicate that 12 weeks of dapagliflozin treatment significantly improved patient-reported symptoms, physical limitations and exercise function and was well tolerated in chronic HFpEF. In a multicenter, randomized trial, the SGLT2 inhibitor dapagliflozin improved the health status and exercise function of patients with heart failure with preserved ejection fraction (HFpEF), a condition for which effective treatments are lacking.
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