Effects of sacubitril/valsartan according to natriuretic peptide levels in patients enrolled in PARADIGM-HF and PARAGON-HF (original) (raw)
Kondo, T. et al. (2025) Effects of sacubitril/valsartan according to natriuretic peptide levels in patients enrolled in PARADIGM-HF and PARAGON-HF.JACC: Heart Failure, 13(6), pp. 927-939. (doi: 10.1016/j.jchf.2024.12.010) (PMID:40088233)
Abstract
Background: Recent trials of new heart failure (HF) treatments suggest the effect of therapy may vary by N-terminal pro–B type natriuretic peptide (NT-proBNP) level. Objectives: The authors examined the efficacy of sacubitril/valsartan according to NT-proBNP levels in patients with reduced, mildly reduced, and preserved left ventricular ejection fraction (LVEF) enrolled in PARADIGM-HF (Prospective Comparison of Angiotensin Receptor–Neprilysin Inhibitor with Angiotensin-Converting–Enzyme Inhibitor to Determine Impact on Global Mortality and Morbidity in Heart Failure Trial) and PARAGON-HF (Prospective Comparison of Angiotensin Receptor–Neprilysin Inhibitor with Angiotensin-Receptor Blockers Global Outcomes in HF with Preserved Ejection Fraction). Methods: Individual patient data from PARADIGM-HF and PARAGON-HF were pooled and participants were divided into categories defined by quintiles of NT-proBNP level. The primary outcome examined was the composite of HF hospitalization or cardiovascular death. Results: Among the 13,195 patients enrolled in both trials, 13,142 (99.6%) had a baseline NT-proBNP level measured. The rate of the primary outcome (per 100 person-years) increased with NT-proBNP levels: quintile 1, 5.9 (95% CI: 5.3-6.5); quintile 2, 7.5 (95% CI: 6.9-8.2); quintile 3, 9.0 (95% CI: 8.2-9.7); quintile 4, 12.0 (95% CI: 11.1-12.9); and quintile 5, 20.8 (95% CI: 19.6-22.2). The relative risk reduction in the primary outcome with sacubitril/valsartan was consistent across NT-proBNP levels: the HR in quintile 1 was 0.79 (95% CI: 0.65-0.96); quintile 2, 0.87 (95% CI: 0.72-1.04); quintile 3, 0.79 (95% CI: 0.66-0.93); quintile 4, 0.85 (95% CI: 0.73-0.99); and quintile 5, 0.86 (95% CI: 0.76-0.97; P for interaction = 0.86). The absolute risk reduction was greatest in NT-proBNP quintile 5; the number needed to treat for the primary outcome over the median follow-up of 31 months was 16 in quintile 5 vs 37 in quintile 1. Conclusions: The relative risk reductions with sacubitril/valsartan were consistent irrespective of NT-proBNP level in HF patients across the range of LVEF. Consequently, the absolute risk reductions were greatest in patients with higher NT-proBNP levels. (PARADIGM-HF; NCT01035255; and PARAGON-HF; NCT01920711).
| Item Type: | Articles |
|---|---|
| Keywords: | Clinical trial, heart failure, natriuretic peptide, outcomes, sacubitril/valsartan. |
| Status: | Published |
| Refereed: | Yes |
| Glasgow Author(s) Enlighten ID: | Docherty, Dr Kieran and Jhund, Professor Pardeep and McMurray, Professor John |
| Authors: | Kondo, T., Jhund, P. S., Anand, I. S., Claggett, B. L., Desai, A. S., Docherty, K. F., Lam, C. S.P., Lefkowitz, M. P., Maggioni, A. P., Martinez, F. A., Redfield, M. M., Rouleau, J. L., Van Veldhuisen, D. J., Zannad, F., Zile, M. R., Packer, M., Solomon, S. D., and McMurray, J. J.V. |
| College/School: | College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health |
| Journal Name: | JACC: Heart Failure |
| Publisher: | Elsevier |
| ISSN: | 2213-1779 |
| ISSN (Online): | 2213-1787 |
| Published Online: | 12 March 2025 |
| Copyright Holders: | Copyright © 2025 The Authors. |
| First Published: | First published in JACC: Heart Failure 13(6): 927-939 |
| Publisher Policy: | Reproduced under a Creative Commons license |
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Funder and Project Information
BHF Centre of Excellence
Colin Berry
RE/18/6/34217
SCMH - Cardiovascular & Metabolic Health
Deposit and Record Details
| ID Code: | 350175 |
|---|---|
| Depositing User: | Ms Jacqui Brannan |
| Datestamp: | 02 Apr 2025 15:20 |
| Last Modified: | 15 Jul 2025 09:44 |
| Date of acceptance: | 13 December 2024 |
| Date of first online publication: | 12 March 2025 |
| Date Deposited: | 2 April 2025 |
| Data Availability Statement: | No |