Impact of vasodilators on diuretic response in patients with congestive heart failure: A mechanistic trial of cimlanod (BMS‐986231)

Author:

Pellicori Pierpaolo1,Cleland John G.F.1,Borentain Maria2,Taubel Jorg3,Graham Fraser J.1,Khan Javed1,Bruzzese Dario4,Kessler Paul2,McMurray John J.V.1,Voors Adriaan A.5,O'Connor Christopher M.6,Teerlink John R.7,Felker G. Michael8

Affiliation:

1. British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular & Metabolic Health University of Glasgow Glasgow UK

2. Bristol Myers Squibb Princeton NJ USA

3. Richmond Pharmacology Ltd, St. George's University of London London UK

4. Department of Public Health University of Naples ‘Federico II’ Naples Italy

5. University of Groningen, Department of Cardiology University Medical Center Groningen Groningen The Netherlands

6. Inova Heart and Vascular Institute Falls Church VA USA

7. Section of Cardiology San Francisco Veterans Affairs Medical Center and School of Medicine, University of California San Francisco San Francisco CA USA

8. Duke University School of Medicine and the Duke Clinical Research Institute Durham NC USA

Abstract

AimTo investigate the effects of Cimlanod, a nitroxyl donor with vasodilator properties, on water and salt excretion after an administration of an intravenos bolus of furosemide.Methods and resultsIn this randomized, double‐blind, mechanistic, crossover trial, 21 patients with left ventricular ejection fraction <45%, increased plasma concentrations of N‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP) and receiving loop diuretics were given, on separate study days, either an 8 h intravenous (IV) infusion of cimlanod (12 μg/kg/min) or placebo. Furosemide was given as a 40 mg IV bolus four hours after the start of infusion. The primary endpoint was urine volume in the 4 h after the bolus of furosemide during infusion of cimlanod compared with placebo. Median NT‐proBNP at baseline was 1487 (interquartile range: 847–2665) ng/L. Infusion of cimlanod increased cardiac output and reduced blood pressure without affecting cardiac power index consistent with its vasodilator effects. Urine volume in the 4 h post‐furosemide was lower with cimlanod (1032 ± 393 ml) versus placebo (1481 ± 560 ml) (p = 0.002), as were total sodium excretion (p = 0.004), fractional sodium excretion (p = 0.016), systolic blood pressure (p < 0.001), estimated glomerular filtration rate (p = 0.012), and haemoglobin (p = 0.010), an index of plasma volume expansion.ConclusionsFor patients with heart failure and congestion, vasodilatation with agents such as cimlanod reduces the response to diuretic agents, which may offset any benefit from acute reductions in cardiac preload and afterload.

Funder

Bristol-Myers Squibb

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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