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

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          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.

          Abstract

          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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          Most cited references35

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          Dapagliflozin in Patients with Heart Failure and Reduced Ejection Fraction

          In patients with type 2 diabetes, inhibitors of sodium-glucose cotransporter 2 (SGLT2) reduce the risk of a first hospitalization for heart failure, possibly through glucose-independent mechanisms. More data are needed regarding the effects of SGLT2 inhibitors in patients with established heart failure and a reduced ejection fraction, regardless of the presence or absence of type 2 diabetes.
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            Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure

            Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce the risk of hospitalization for heart failure in patients regardless of the presence or absence of diabetes. More evidence is needed regarding the effects of these drugs in patients across the broad spectrum of heart failure, including those with a markedly reduced ejection fraction.
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              Angiotensin–Neprilysin Inhibition in Heart Failure with Preserved Ejection Fraction

              The angiotensin receptor-neprilysin inhibitor sacubitril-valsartan led to a reduced risk of hospitalization for heart failure or death from cardiovascular causes among patients with heart failure and reduced ejection fraction. The effect of angiotensin receptor-neprilysin inhibition in patients with heart failure with preserved ejection fraction is unclear.
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                Author and article information

                Contributors
                mkosiborod@saint-lukes.org
                Journal
                Nat Med
                Nat Med
                Nature Medicine
                Nature Publishing Group US (New York )
                1078-8956
                1546-170X
                28 October 2021
                28 October 2021
                2021
                : 27
                : 11
                : 1954-1960
                Affiliations
                [1 ]GRID grid.419820.6, ISNI 0000 0004 0383 1037, Saint Luke’s Mid America Heart Institute, ; Kansas City, MO USA
                [2 ]GRID grid.266756.6, ISNI 0000 0001 2179 926X, Present Address: University of Missouri-Kansas City, ; Kansas City, MO USA
                [3 ]GRID grid.66875.3a, ISNI 0000 0004 0459 167X, Department of Cardiovascular Medicine, , Mayo Clinic, ; Rochester, MN USA
                [4 ]GRID grid.241167.7, ISNI 0000 0001 2185 3318, Department of Internal Medicine, , Sections on Cardiovascular Medicine and Geriatrics, Wake Forest School of Medicine, ; Winston-Salem, NC USA
                [5 ]GRID grid.16753.36, ISNI 0000 0001 2299 3507, Division of Cardiology, Department of Medicine and Bluhm Cardiovascular Institute, , Northwestern University Feinberg School of Medicine, ; Chicago, IL USA
                [6 ]GRID grid.189967.8, ISNI 0000 0001 0941 6502, Emory University, ; Atlanta, GA USA
                [7 ]GRID grid.488776.2, First Coast Cardiovascular Institute, ; Jacksonville, FL USA
                [8 ]GRID grid.21107.35, ISNI 0000 0001 2171 9311, Johns Hopkins University School of Medicine, ; Baltimore, MD USA
                [9 ]Chicago Medical Research, Hazel Crest, IL USA
                [10 ]GRID grid.240372.0, ISNI 0000 0004 0400 4439, NorthShore University HealthSystem, ; Evanston, IL USA
                [11 ]GRID grid.223827.e, ISNI 0000 0001 2193 0096, University of Utah, ; Salt Lake City, UT USA
                [12 ]Ascension St. Vincent, Indianapolis, IN USA
                [13 ]GRID grid.411024.2, ISNI 0000 0001 2175 4264, Division of Cardiovascular Medicine, , University of Maryland School of Medicine, ; Baltimore, MD USA
                [14 ]GRID grid.490009.4, Stormont Vail Health, ; Topeka, KS USA
                [15 ]GRID grid.417046.0, ISNI 0000 0004 0454 5075, Cardiovascular Institute, , Allegheny Health Network, ; Pittsburgh, PA USA
                [16 ]Heart Group of the Eastern Shore, Fairhope, AL USA
                [17 ]GRID grid.255414.3, ISNI 0000 0001 2182 3733, Eastern Virginia Medical School, ; Norfolk, VA USA
                [18 ]GRID grid.32224.35, ISNI 0000 0004 0386 9924, Cardiology Division, , Massachusetts General Hospital, ; Boston, MA USA
                [19 ]GRID grid.429881.e, ISNI 0000 0004 0453 2696, OSF HealthCare Cardiovascular Institute, ; Peoria, IL USA
                [20 ]GRID grid.42505.36, ISNI 0000 0001 2156 6853, University of Southern California, ; Los Angeles, CA USA
                [21 ]GRID grid.415508.d, ISNI 0000 0001 1964 6010, The George Institute for Global Health, ; Sydney, New South Wales Australia
                [22 ]GRID grid.1005.4, ISNI 0000 0004 4902 0432, University of New South Wales, ; Sydney, New South Wales Australia
                Author information
                http://orcid.org/0000-0001-9375-0596
                http://orcid.org/0000-0002-5655-8201
                http://orcid.org/0000-0002-0874-7059
                http://orcid.org/0000-0002-3750-9789
                Article
                1536
                10.1038/s41591-021-01536-x
                8604725
                34711976
                8ea2ef9e-37d5-434b-ad34-8d7a3b83f8d5
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 19 August 2021
                : 10 September 2021
                Funding
                Funded by: AstraZeneca Study Number: ESR-16-12141
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature America, Inc. 2021

                Medicine
                heart failure,outcomes research
                Medicine
                heart failure, outcomes research

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