Cardiac and Metabolic Effects of Dapagliflozin in Heart Failure With Preserved Ejection Fraction: The CAMEO-DAPA Trial.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
05 09 2023
Historique:
pmc-release: 05 09 2024
medline: 7 9 2023
pubmed: 3 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

Sodium-glucose cotransporter-2 inhibitors reduce risk of hospitalization for heart failure in patients who have heart failure with preserved ejection fraction (HFpEF), but the hemodynamic mechanisms underlying these benefits remain unclear. This study sought to determine whether treatment with dapagliflozin affects pulmonary capillary wedge pressure (PCWP) at rest and during exercise in patients with HFpEF. This was a single-center, double-blinded, randomized, placebo-controlled trial testing the effects of 10 mg of dapagliflozin once daily in patients with HFpEF. Patients with New York Heart Association class II or III heart failure, ejection fraction ≥50%, and elevated PCWP during exercise were recruited. Cardiac hemodynamics were measured at rest and during exercise using high-fidelity micromanometers at baseline and after 24 weeks of treatment. The primary end point was a change from baseline in rest and peak exercise PCWPs that incorporated both measurements, and was compared using a mixed-model likelihood ratio test. Key secondary end points included body weight and directly measured blood and plasma volumes. Expired gas analysis was performed evaluate oxygen transport in tandem with arterial lactate sampling. Among 38 patients completing baseline assessments (median age 68 years; 66% women; 71% obese), 37 completed the trial. Treatment with dapagliflozin resulted in reduction in the primary end point of change in PCWP at rest and during exercise at 24 weeks relative to treatment with placebo (likelihood ratio test for overall changes in PCWP; In patients with HFpEF, treatment with dapagliflozin reduces resting and exercise PCWP, along with the favorable effects on plasma volume and body weight. These findings provide new insight into the hemodynamic mechanisms of benefit with sodium-glucose cotransporter-2 inhibitors in HFpEF. URL: https://www. gov; Unique identifier: NCT04730947.

Sections du résumé

BACKGROUND
Sodium-glucose cotransporter-2 inhibitors reduce risk of hospitalization for heart failure in patients who have heart failure with preserved ejection fraction (HFpEF), but the hemodynamic mechanisms underlying these benefits remain unclear. This study sought to determine whether treatment with dapagliflozin affects pulmonary capillary wedge pressure (PCWP) at rest and during exercise in patients with HFpEF.
METHODS
This was a single-center, double-blinded, randomized, placebo-controlled trial testing the effects of 10 mg of dapagliflozin once daily in patients with HFpEF. Patients with New York Heart Association class II or III heart failure, ejection fraction ≥50%, and elevated PCWP during exercise were recruited. Cardiac hemodynamics were measured at rest and during exercise using high-fidelity micromanometers at baseline and after 24 weeks of treatment. The primary end point was a change from baseline in rest and peak exercise PCWPs that incorporated both measurements, and was compared using a mixed-model likelihood ratio test. Key secondary end points included body weight and directly measured blood and plasma volumes. Expired gas analysis was performed evaluate oxygen transport in tandem with arterial lactate sampling.
RESULTS
Among 38 patients completing baseline assessments (median age 68 years; 66% women; 71% obese), 37 completed the trial. Treatment with dapagliflozin resulted in reduction in the primary end point of change in PCWP at rest and during exercise at 24 weeks relative to treatment with placebo (likelihood ratio test for overall changes in PCWP;
CONCLUSIONS
In patients with HFpEF, treatment with dapagliflozin reduces resting and exercise PCWP, along with the favorable effects on plasma volume and body weight. These findings provide new insight into the hemodynamic mechanisms of benefit with sodium-glucose cotransporter-2 inhibitors in HFpEF.
REGISTRATION
URL: https://www.
CLINICALTRIALS
gov; Unique identifier: NCT04730947.

Identifiants

pubmed: 37534453
doi: 10.1161/CIRCULATIONAHA.123.065134
pmc: PMC10529848
mid: NIHMS1919521
doi:

Substances chimiques

dapagliflozin 1ULL0QJ8UC
Lactates 0
Sodium-Glucose Transporter 2 Inhibitors 0

Banques de données

ClinicalTrials.gov
['NCT04730947']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

834-844

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL128526
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL162828
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL160226
Pays : United States

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Auteurs

Barry A Borlaug (BA)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.

Yogesh N V Reddy (YNV)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.

Amanda Braun (A)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.

Hidemi Sorimachi (H)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.
Department of Cardiovascular Medicine, Gumma University Graduate School of Medicine, Japan (H.S.).

Massar Omar (M)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.
Department of Cardiology (M.O.), Odense University Hospital, Denmark (M.O).
Steno Diabetes Center, Odense University Hospital, Denmark (M.O).

Dejana Popovic (D)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.
Division of Cardiology, University Clinical Center of Serbia, Belgrade (D.J.).

Alessio Alogna (A)

Departments of Cardiovascular Medicine (B.A.B., Y.N.V.R., A.B., H.S., M.O., D.P., A.A.), Mayo Clinic, Rochester, MN.
German Heart Center of the Charité, Campus Virchow-Klinikum and German Centre for Cardiovascular Research Partner Site, Berlin, Germany (A.A.).

Michael D Jensen (MD)

Medicine, Division of Endocrinology, Diabetes and Metabolism (M.D.J.), Mayo Clinic, Rochester, MN.

Rickey Carter (R)

Department of Quantitative Health Sciences, Division of Clinical Trials and Biostatistics, Mayo Clinic, Jacksonville, FL (R.C.).

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