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
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 type: Journal Article
Publication date: 2021-10-28
Journal:
Nature Medicine
scimago Q1
SJR: 19.045
CiteScore: 100.9
Impact factor: 58.7
ISSN: 10788956, 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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