Global Differences in Heart Failure With Preserved Ejection Fraction: The PARAGON-HF Trial.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
04 2021
Historique:
pubmed: 20 4 2021
medline: 12 10 2021
entrez: 19 4 2021
Statut: ppublish

Résumé

Heart failure with preserved ejection fraction (HFpEF) is a global public health problem with important regional differences. We investigated these differences in the PARAGON-HF trial (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin Receptor Blocker Global Outcomes in HFpEF), the largest and most inclusive global HFpEF trial. We studied differences in clinical characteristics, outcomes, and treatment effects of sacubitril/valsartan in 4796 patients with HFpEF from the PARAGON-HF trial, grouped according to geographic region. Regional differences in patient characteristics and comorbidities were observed: patients from Western Europe were oldest (mean 75±7 years) with the highest prevalence of atrial fibrillation/flutter (36%); Central/Eastern European patients were youngest (mean 71±8 years) with the highest prevalence of coronary artery disease (50%); North American patients had the highest prevalence of obesity (65%) and diabetes (49%); Latin American patients were younger (73±9 years) and had a high prevalence of obesity (53%); and Asia-Pacific patients had a high prevalence of diabetes (44%), despite a low prevalence of obesity (26%). Rates of the primary composite end point of total hospitalizations for HF and death from cardiovascular causes were lower in patients from Central Europe (9 per 100 patient-years) and highest in patients from North America (28 per 100 patient-years), which was primarily driven by a greater number of total hospitalizations for HF. The effect of treatment with sacubitril-valsartan was not modified by region (interaction Among patients with HFpEF recruited worldwide in PARAGON-HF, there were important regional differences in clinical characteristics and outcomes, which may have implications for the design of future clinical trials. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01920711.

Sections du résumé

BACKGROUND
Heart failure with preserved ejection fraction (HFpEF) is a global public health problem with important regional differences. We investigated these differences in the PARAGON-HF trial (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin Receptor Blocker Global Outcomes in HFpEF), the largest and most inclusive global HFpEF trial.
METHODS
We studied differences in clinical characteristics, outcomes, and treatment effects of sacubitril/valsartan in 4796 patients with HFpEF from the PARAGON-HF trial, grouped according to geographic region.
RESULTS
Regional differences in patient characteristics and comorbidities were observed: patients from Western Europe were oldest (mean 75±7 years) with the highest prevalence of atrial fibrillation/flutter (36%); Central/Eastern European patients were youngest (mean 71±8 years) with the highest prevalence of coronary artery disease (50%); North American patients had the highest prevalence of obesity (65%) and diabetes (49%); Latin American patients were younger (73±9 years) and had a high prevalence of obesity (53%); and Asia-Pacific patients had a high prevalence of diabetes (44%), despite a low prevalence of obesity (26%). Rates of the primary composite end point of total hospitalizations for HF and death from cardiovascular causes were lower in patients from Central Europe (9 per 100 patient-years) and highest in patients from North America (28 per 100 patient-years), which was primarily driven by a greater number of total hospitalizations for HF. The effect of treatment with sacubitril-valsartan was not modified by region (interaction
CONCLUSIONS
Among patients with HFpEF recruited worldwide in PARAGON-HF, there were important regional differences in clinical characteristics and outcomes, which may have implications for the design of future clinical trials. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01920711.

Identifiants

pubmed: 33866828
doi: 10.1161/CIRCHEARTFAILURE.120.007901
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Valsartan 80M03YXJ7I
Neprilysin EC 3.4.24.11
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Banques de données

ClinicalTrials.gov
['NCT01920711']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007901

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR001424
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG059988
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK092923
Pays : United States
Organisme : NHLBI NIH HHS
ID : R21 HL085375
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL069771
Pays : United States

Auteurs

Jasper Tromp (J)

National Heart Centre Singapore (J.T., C.S.P.L.).
Duke-NUS Medical School, Singapore (J.T., C.S.P.L.).
Department of Cardiology, University Medical Centre Groningen, University of Groningen, the Netherlands (J.T., D.J.V.V., C.S.P.L.).
Saw Swee Hock School of Public Health, National University of Singapore, Singapore (J.T.).

Brian L Claggett (BL)

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

Jiankang Liu (J)

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

Alice M Jackson (AM)

British Heart Foundation Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom (A.M.J., P.S.J., J.J.V.M.).

Pardeep S Jhund (PS)

British Heart Foundation Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom (A.M.J., P.S.J., J.J.V.M.).

Lars Køber (L)

Department of Cardiology, Heart Centre, Rigshospitalet, Copenhagen University Hospital, Denmark (L.K.).

Jiří Widimský (J)

First Faculty of Medicine, Charles University Prague, Czech Republic (J.W.).

Sergey A Boytsov (SA)

National Research Center for Cardiology of the Ministry of Health of the Russian Federation, Moscow (S.B.).

Vijay K Chopra (VK)

Heart Failure and Research Max Super Specialty Hospital Saket, New Delhi, India (V.C.).

Inder S Anand (IS)

Department of Medicine, VA Medical Center and University of Minnesota, Minneapolis (I.S.A.).

Junbo Ge (J)

Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, China (J.G.).

Chen-Huan Chen (CH)

Faculty of Medicine, National Yang-Ming University, Taipei, Taiwan, Republic of China (C.-H.C.).

Aldo P Maggioni (AP)

Associazione Nazionale Medici Cardiologi Ospedalieri, Florence, Italy (A.P.M.).

Felipe Martinez (F)

Universidad Nacional of Cordoba, Argentina (F.M.).

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX (M.P.).

Marc A Pfeffer (MA)

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

Burkert Pieske (B)

Department of Internal Medicine, Cardiology Charité, Universitaetsmedizin Berlin, Campus Virchow Klinikum Berlin, Germany (B.P.).

Margaret M Redfield (MM)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN (M.M.R.).

Jean L Rouleau (JL)

Institut de Cardiologie de Montréal, Université de Montréal, QC, Canada (J.L.R.).

Dirk J Van Veldhuisen (DJ)

Department of Cardiology, University Medical Centre Groningen, University of Groningen, the Netherlands (J.T., D.J.V.V., C.S.P.L.).

Faiez Zannad (F)

Inserm CIC 1433 and Université de Lorraine, Centre Hospitalier Régional Universitaire, Nancy, France (F.Z.).

Michael R Zile (MR)

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

Adel R Rizkala (AR)

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

Akiko Inubushi-Molessa (A)

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

Martin P Lefkowitz (MP)

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

Victor C Shi (VC)

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

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom (A.M.J., P.S.J., J.J.V.M.).

Scott D Solomon (SD)

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

Carolyn S P Lam (CSP)

National Heart Centre Singapore (J.T., C.S.P.L.).
Duke-NUS Medical School, Singapore (J.T., C.S.P.L.).
Department of Cardiology, University Medical Centre Groningen, University of Groningen, the Netherlands (J.T., D.J.V.V., C.S.P.L.).

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH