Influence of Atrial Fibrillation on Post-Discharge Natriuretic Peptide Trajectory and Clinical Outcomes Among Patients Hospitalized for Heart Failure: Insights from the ASTRONAUT Trial
Year: 2016
Type: article
Abstract: AIMS: Change in NT-proBNP level is a common surrogate endpoint in early phase heart failure (HF) trials, but whether this endpoint is influenced by atrial fibrillation/flutter (AFF) is unclear. METHODS AND RESULTS: This analysis included 1358 patients from the ASTRONAUT trial, which randomized patients hospitalized for HF with EF ≤40% to aliskiren or placebo in addition to standard care. Patients were stratified by presence of AFF on baseline ECG. NT-proBNP was measured longitudinally by a core laboratory at baseline, 1 month, 6 months, and 12 months. Compared with non-AFF patients, AFF patients experienced greater reduction from baseline in log-transformed NT-proBNP (interaction P < 0.001), but this difference was not significant after adjustment (interaction P = 0.726). The ability of aliskiren to lower NT-proBNP during follow-up differed by AFF status (interaction P = 0.001), with aliskiren lowering NT-proBNP more than placebo among non-AFF patients only. After adjustment, baseline AFF was not associated with mortality or HF hospitalization at 12 months (all P ≥ 0.152). CONCLUSION: In this hospitalized HF cohort, AFF status did not influence post-discharge NT-proBNP trajectory or clinical outcomes after adjustment for patient characteristics. Aliskiren lowered follow-up NT-proBNP levels in patients without AFF, but had no influence among patients with AFF. This study generates the hypothesis that the ability of a HF trial to meet an NT-proBNP defined endpoint may be influenced by the prevalence of AFF in the population. Because aliskiren did not improve outcomes in patients without AFF, this analysis suggests changes in NT-proBNP induced by investigational therapies may be dissociated from clinical effects.
DOI: 10.1002/ejhf.674
Authors: Stephen J. Greene, Gregg C. Fonarow, Scott D. Solomon, Haris P. Subacius, Andrew P. Ambrosy, Muthiah Vaduganathan, Aldo P. Maggioni, Michael Böhm, Eldrin F. Lewis, Faiez Zannad, Javed Butler, Mihai Gheorghiade, for the ASTRONAUT Investigators and Coordinators
Institutions: Duke Medical Center, University of California, Los Angeles, Brigham and Women's Hospital, Northwestern University, Associazione Nazionale Medici Cardiologi Ospedalieri, Universitätsklinikum des Saarlandes, Inserm, Centre Hospitalier Régional et Universitaire de Nancy, Université de Lorraine, Stony Brook University
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: Boehringer Ingelheim, Amgen, ResMed Foundation, AstraZeneca, Bayer, Novartis, Takeda Pharmaceuticals U.S.A., Boston Scientific Corporation, Ahmanson Foundation, BG Medicine, ResMed, Servier, National Institutes of Health, Johnson and Johnson, GE Healthcare, Feinberg School of Medicine, Abbott Vascular, Roche Diagnostics, Relypsa, National Heart, Lung, and Blood Institute
OpenAlex ID: W2539231244
