Urinary cGMP (Cyclic Guanosine Monophosphate)/BNP (B-Type Natriuretic Peptide) Ratio, Sacubitril/Valsartan, and Outcomes in Heart Failure With Reduced Ejection Fraction: An Analysis of the PARADIGM-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:
03 2023
Historique:
entrez: 21 3 2023
pubmed: 22 3 2023
medline: 24 3 2023
Statut: ppublish

Résumé

The ratio of ucGMP (urinary cyclic guanosine monophosphate) to BNP (B-type natriuretic peptide) is thought to reflect the responsiveness of tissues to natriuretic peptides. We examined the relationship between ucGMP/BNP ratio and clinical outcomes, the effect of sacubitril/valsartan, compared with enalapril, on the ucGMP/BNP ratio, and the efficacy of sacubitril/valsartan on clinical outcomes according to baseline ucGMP/BNP ratio in PARADIGM-HF trial (Prospective Comparison of ARNI With ACEI to Determine Impact on Global Mortality and Morbidity in Heart Failure). ucGMP/BNP ratio was available at baseline (N=2031), 1 month (N=1959), and 8 months after randomization (N=1746). The primary outcome was a composite of heart failure hospitalization or cardiovascular death. Compared with the lowest tertile of baseline ucGMP/BNP ratio, patients in the higher tertiles had a lower risk of the primary outcome (tertile 1, reference; tertile 2, hazard ratio 0.57 [95% CI, 0.45-0.71]; tertile 3, hazard ratio, 0.54 [0.43-0.67]). Compared with baseline, the ucGMP/BNP ratio at 1 month and 8 months after randomization was higher with sacubitril/valsartan than with enalapril: ratio of geometric mean ratios at 1 month, 1.38 (95% CI, 1.27-1.51) and 8 months, 1.32 (95% CI, 1.20-1.45), and this difference was consistent across tertiles of ucGMP/BNP ratio at baseline ( In patients with heart failure and reduced ejection fraction, higher ucGMP/BNP ratio was associated with better outcomes. Sacubitril/valsartan increased the ucGMP/BNP ratio, compared with enalapril, and the effect of sacubitril/valsartan on clinical outcomes was not modified by baseline ucGMP/BNP ratio. URL: https://www. gov; Unique Identifier: NCT01035255.

Sections du résumé

BACKGROUND
The ratio of ucGMP (urinary cyclic guanosine monophosphate) to BNP (B-type natriuretic peptide) is thought to reflect the responsiveness of tissues to natriuretic peptides.
METHODS
We examined the relationship between ucGMP/BNP ratio and clinical outcomes, the effect of sacubitril/valsartan, compared with enalapril, on the ucGMP/BNP ratio, and the efficacy of sacubitril/valsartan on clinical outcomes according to baseline ucGMP/BNP ratio in PARADIGM-HF trial (Prospective Comparison of ARNI With ACEI to Determine Impact on Global Mortality and Morbidity in Heart Failure). ucGMP/BNP ratio was available at baseline (N=2031), 1 month (N=1959), and 8 months after randomization (N=1746). The primary outcome was a composite of heart failure hospitalization or cardiovascular death.
RESULTS
Compared with the lowest tertile of baseline ucGMP/BNP ratio, patients in the higher tertiles had a lower risk of the primary outcome (tertile 1, reference; tertile 2, hazard ratio 0.57 [95% CI, 0.45-0.71]; tertile 3, hazard ratio, 0.54 [0.43-0.67]). Compared with baseline, the ucGMP/BNP ratio at 1 month and 8 months after randomization was higher with sacubitril/valsartan than with enalapril: ratio of geometric mean ratios at 1 month, 1.38 (95% CI, 1.27-1.51) and 8 months, 1.32 (95% CI, 1.20-1.45), and this difference was consistent across tertiles of ucGMP/BNP ratio at baseline (
CONCLUSIONS
In patients with heart failure and reduced ejection fraction, higher ucGMP/BNP ratio was associated with better outcomes. Sacubitril/valsartan increased the ucGMP/BNP ratio, compared with enalapril, and the effect of sacubitril/valsartan on clinical outcomes was not modified by baseline ucGMP/BNP ratio.
REGISTRATION
URL: https://www.
CLINICALTRIALS
gov; Unique Identifier: NCT01035255.

Identifiants

pubmed: 36943907
doi: 10.1161/CIRCHEARTFAILURE.122.010111
pmc: PMC10022671
doi:

Substances chimiques

Natriuretic Peptide, Brain 114471-18-0
sacubitril 17ERJ0MKGI
Guanosine Monophosphate 85-32-5
Angiotensin-Converting Enzyme Inhibitors 0
Tetrazoles 0
Angiotensin Receptor Antagonists 0
Valsartan 80M03YXJ7I
Enalapril 69PN84IO1A
Aminobutyrates 0
Biphenyl Compounds 0
Drug Combinations 0

Banques de données

ClinicalTrials.gov
['NCT01035255']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010111

Subventions

Organisme : British Heart Foundation
Pays : United Kingdom

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Auteurs

Jawad H Butt (JH)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (J.H.B., W.I., P.D., P.S.J., J.J.V.M.).
Department of Cardiology, Copenhagen University Hospital-Rigshospitalet, Denmark (J.H.B., L.K.).

Wasyla Ibrahim (W)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (J.H.B., W.I., P.D., P.S.J., J.J.V.M.).

Pooja Dewan (P)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (J.H.B., W.I., P.D., P.S.J., J.J.V.M.).

Akshay S Desai (AS)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (A.S.D., S.D.S.).

Lars Køber (L)

Department of Cardiology, Copenhagen University Hospital-Rigshospitalet, Denmark (J.H.B., L.K.).

Margaret F Prescott (MF)

Novartis Pharmaceuticals Corporation, East Hanover, NJ (M.F.P., M.P.L.).

Martin P Lefkowitz (MP)

Novartis Pharmaceuticals Corporation, East Hanover, NJ (M.F.P., M.P.L.).

Jean L Rouleau (JL)

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

Scott D Solomon (SD)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (A.S.D., S.D.S.).

Michael R Zile (MR)

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

Milton Packer (M)

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

Pardeep S Jhund (PS)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (J.H.B., W.I., P.D., P.S.J., J.J.V.M.).

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (J.H.B., W.I., P.D., P.S.J., J.J.V.M.).

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