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Natriuretic peptide plasma concentrations and risk of cardiovascular versus non-cardiovascular events in heart failure with reduced ejection fraction: Insights from the PARADIGM-HF and ATMOSPHERE trials - 26/05/21

Doi : 10.1016/j.ahj.2021.02.015 
Muhammad Shahzeb Khan, MD, MSc a, , Soren Lund Kristensen, MD, PhD b, , Muthiah Vaduganathan, MD, MPH c, Lars Kober, MD, DMSc b, William T Abraham, MD d, Akshay S Desai, MD, MPH c, Scott D Solomon, MD c, Karl Swedberg, MD, PhD e, Kenneth Dickstein, MD, PhD f, Michael R Zile, MD g, Milton Packer, MD h, John JV. McMurray, MD i, Javed Butler, MD, MPH, MBA a,
a Department of Medicine, University of Mississippi, Jackson, MS 
b Division of Cardiology, Rigshospitalet University Hospital, Copenhagen, Denmark 
c Brigham and Women's Hospital Heart & Vascular Center, Boston, MA 
d Division of Cardiovascular Medicine, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH 
e Department of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden 
f Department of Cardiology, University of Bergen, Stavanger University Hospital, Stavanger, Norway 
g Division of Cardiology, Medical University of South Carolina, and Ralph H Johnson Veterans Administration Medical Centre, Charleston, SC 
h Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX 
i BHF Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom 

#Reprint requests: Javed Butler, MD MPH MBA, Department of Medicine, University of Mississippi Medical Center, 2500 N. State Street, Jackson, MS 39216.Department of MedicineUniversity of Mississippi Medical Center2500 N. State StreetJacksonMS39216

Abstract

Background

: N-terminal pro-B-type natriuretic peptide (NT-proBNP) plasma concentrations are independent prognostic markers in patients with heart failure and reduced ejection fraction (HFrEF). Whether a differential risk association between NT-proBNP plasma concentrations and risk of cardiovascular (CV) vs non-CV adverse events exists is not well known.

Objective

: To assess if there is a differential proportional risk of CV vs non-CV adverse events by NT-proBNP plasma concentrations.

Methods

: In this post hoc combined analysis of PARADIGM-HF and ATMOSPHERE trials, proportion of CV vs non-CV mortality and hospitalizations were assessed by NT-proBNP levels (<400, 400-999, 1000-1999, 2000-2999, and >3000 pg/mL) at baseline using Cox regression adjusting for traditional risk factors.

Results

: A total of 14,737 patients with mean age of 62 ± 8 years (24% history of atrial fibrillation [AF]) were studied. For CV deaths, the event rates per 1000 patient-years steeply increased from 33.8 in the ≤400 pg/mL group to 142.3 in the ≥3000 pg/mL group, while the non-CV death event rates modestly increased from 9.0 to 22.7, respectively. Proportion of non-CV deaths decreased across the 5 NT-proBNP groups (21.1%, 18.4%, 17.9%, 17.4%, and 13.7% respectively). Similar trend was observed for non-CV hospitalizations (46.4%, 42.6%, 42.9%, 42.0%, and 36.9% respectively). These results remained similar when stratified according to the presence of AF at baseline and prior HF hospitalization within last 12 months.

Conclusions

: The absolute CV event rates per patient years of follow-up were greater and had higher stepwise increases than non-CV event rates across a broad range of NT-proBNP plasma concentrations indicating a differential risk of CV events at varying baseline NT-proBNP values. These results have implications for future design of clinical trials.

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Vol 237

P. 45-53 - Luglio 2021 Ritorno al numero
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