Effects of Sacubitril-Valsartan Versus Valsartan in Women Compared With Men With Heart Failure and Preserved Ejection Fraction: Insights From PARAGON-HF.


Journal

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

Informations de publication

Date de publication:
04 02 2020
Historique:
pubmed: 19 11 2019
medline: 13 8 2020
entrez: 19 11 2019
Statut: ppublish

Résumé

Unlike heart failure with reduced ejection fraction, there is no approved treatment for heart failure with preserved ejection fraction, the predominant phenotype in women. Therefore, there is a greater heart failure therapeutic deficit in women compared with men. In a prespecified subgroup analysis, we examined outcomes according to sex in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in Heart Failure With Preserved Ejection Fraction), which compared sacubitril-valsartan and valsartan in patients with heart failure with preserved ejection fraction. The primary outcome was a composite of first and recurrent hospitalizations for heart failure and death from cardiovascular causes. We also report secondary efficacy and safety outcomes. Overall, 2479 women (51.7%) and 2317 men (48.3%) were randomized. Women were older and had more obesity, less coronary disease, and lower estimated glomerular filtration rate and NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels than men. For the primary outcome, the rate ratio for sacubitril-valsartan versus valsartan was 0.73 (95% CI, 0.59-0.90) in women and 1.03 (95% CI, 0.84-1.25) in men ( As compared with valsartan, sacubitril-valsartan seemed to reduce the risk of heart failure hospitalization more in women than in men. Whereas the possible sex-related modification of the effect of treatment has several potential explanations, the present study does not provide a definite mechanistic basis for this finding. https://www.clinicaltrials.gov. Unique identifier: NCT01920711.

Sections du résumé

BACKGROUND
Unlike heart failure with reduced ejection fraction, there is no approved treatment for heart failure with preserved ejection fraction, the predominant phenotype in women. Therefore, there is a greater heart failure therapeutic deficit in women compared with men.
METHODS
In a prespecified subgroup analysis, we examined outcomes according to sex in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in Heart Failure With Preserved Ejection Fraction), which compared sacubitril-valsartan and valsartan in patients with heart failure with preserved ejection fraction. The primary outcome was a composite of first and recurrent hospitalizations for heart failure and death from cardiovascular causes. We also report secondary efficacy and safety outcomes.
RESULTS
Overall, 2479 women (51.7%) and 2317 men (48.3%) were randomized. Women were older and had more obesity, less coronary disease, and lower estimated glomerular filtration rate and NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels than men. For the primary outcome, the rate ratio for sacubitril-valsartan versus valsartan was 0.73 (95% CI, 0.59-0.90) in women and 1.03 (95% CI, 0.84-1.25) in men (
CONCLUSIONS
As compared with valsartan, sacubitril-valsartan seemed to reduce the risk of heart failure hospitalization more in women than in men. Whereas the possible sex-related modification of the effect of treatment has several potential explanations, the present study does not provide a definite mechanistic basis for this finding.
CLINICAL TRIAL REGISTRATION
https://www.clinicaltrials.gov. Unique identifier: NCT01920711.

Identifiants

pubmed: 31736337
doi: 10.1161/CIRCULATIONAHA.119.044491
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Biphenyl Compounds 0
Drug Combinations 0
Tetrazoles 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Banques de données

ClinicalTrials.gov
['NCT01920711']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

338-351

Subventions

Organisme : British Heart Foundation
ID : RE/18/6/34217
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/18/14/33330
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

John J V McMurray (JJV)

BHF Cardiovascular Research Centre, University of Glasgow, UK (J.J.V.M., A.M.J., P.S.J.).

Alice M Jackson (AM)

BHF Cardiovascular Research Centre, University of Glasgow, UK (J.J.V.M., A.M.J., P.S.J.).

Carolyn S P Lam (CSP)

National Heart Center Singapore and Duke-National University of Singapore (C.S.P.L.).
Department of Cardiology, University Medical Center Groningen, University of Groningen, The Netherlands (C.S.P.L., D.J.v.V.).
The George Institute for Global Health, Newtown, Australia (C.S.P.L.).

Margaret M Redfield (MM)

Mayo Clinic, Rochester, MN (M.M.R.).

Inder S Anand (IS)

University of Minnesota, Minneapolis (I.S.A.).

Junbo Ge (J)

Shanghai Institute of Cardiovascular Diseases, China (J.G.).

Marty P Lefkowitz (MP)

Novartis Pharmaceuticals, East Hanover, NJ (M.P.L., A.R.R., S.V.S., V.C.S.).

Aldo P Maggioni (AP)

National Association of Hospital Cardiologists Research Center, Florence, Italy (A.P.M.).

Felipe Martinez (F)

National University of Cordoba, Argentina (F.M.).

Milton Packer (M)

Baylor University Medical Center, Dallas, TX (M.P.).

Marc A Pfeffer (MA)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.A.P., A.M.S., B.C., S.D.S.).

Burkert Pieske (B)

Department of Internal Medicine and Cardiology, German Center for Cardiovascular Research Partner Site Berlin, Germany (B.P.).

Adel R Rizkala (AR)

Novartis Pharmaceuticals, East Hanover, NJ (M.P.L., A.R.R., S.V.S., V.C.S.).

Shalini V Sabarwal (SV)

Novartis Pharmaceuticals, East Hanover, NJ (M.P.L., A.R.R., S.V.S., V.C.S.).

Amil M Shah (AM)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.A.P., A.M.S., B.C., S.D.S.).

Sanjiv J Shah (SJ)

Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL (S.J.S.).

Victor C Shi (VC)

Novartis Pharmaceuticals, East Hanover, NJ (M.P.L., A.R.R., S.V.S., V.C.S.).

Dirk J van Veldhuisen (DJ)

Department of Cardiology, University Medical Center Groningen, University of Groningen, The Netherlands (C.S.P.L., D.J.v.V.).

Faiez Zannad (F)

INSERM Centre d'Investigation Clinic 1433 and Universite de Lorraine, Centre Hospitalier Regional et Universitaire, Nancy, France (F.Z.).

Michael R Zile (MR)

Medical University of South Carolina and the Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston (M.R.Z.).

Maja Cikes (M)

Department of Cardiovascular Diseases, University of Zagreb School of Medicine and University Hospital Centre Zagreb, Croatia (M.C.).

Eva Goncalvesova (E)

Department of Heart Failure-Transplantation, National Cardiovascular Institute, Bratislava, Slovakia (E.G.).

Tzvetana Katova (T)

Clinic of Cardiology, National Cardiology Hospital, Sofia, Bulgaria (T.K.).

Anamaria Kosztin (A)

Heart and Vascular Center, Semmelweis University, Budapest, Hungary (A.K.).

Malgorzata Lelonek (M)

Department of Noninvasive Cardiology, Medical University of Lodz, Poland (M.L.).

Nancy Sweitzer (N)

University of Arizona Sarver Heart, Tucson (N.S.).

Orly Vardeny (O)

Minneapolis VA Center for Care Delivery and Outcomes Research, University of Minnesota (O.V.).

Brian Claggett (B)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.A.P., A.M.S., B.C., S.D.S.).

Pardeep S Jhund (PS)

BHF Cardiovascular Research Centre, University of Glasgow, UK (J.J.V.M., A.M.J., P.S.J.).

Scott D Solomon (SD)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.A.P., A.M.S., B.C., S.D.S.).

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Classifications MeSH