Key result
Oral treatment with the ET(A) receptor antagonist darusentan for 21 days significantly reduced BNP plasma levels and increased the cGMP:BNP ratio in patients with chronic heart failure.
Why the study?
Does oral darusentan improve the cGMP:BNP ratio in patients with chronic heart failure?
RCT (n=142)
Double-blind
randomized
Yes
Does oral darusentan improve the cGMP:BNP ratio in patients with chronic heart failure?
Short-term treatment with the ET(A) receptor antagonist darusentan improves the cGMP:BNP ratio and reduces BNP levels in patients with chronic heart failure, suggesting favorable modulation of the natriuretic peptide system.
Answers are grounded in this paper and cite their sources.
Supports short-term ET(A) antagonism to enhance natriuretic peptide signaling in chronic HF; extends prior infusion findings to oral therapy.
In heart failure, the cGMP to natriuretic peptide ratio is decreased and infusion of atrial natriuretic peptide (ANP) induces less cGMP generation. The ratio of the second messenger cGMP to plasma concentrations of ANP or brain natriuretic peptide (BNP) correlates with the effectiveness of natriuretic peptides. It was investigated whether blockade of the ET(A) receptor might improve the cGMP:NP ratio in heart failure. Patients with chronic heart failure (n=142; mean age=57 years) received oral treatment with the ET(A) antagonist darusentan (either 30, 100, 300 mg/day or placebo) on top of standard therapy over a period of 21 days in a randomized, double-blind, placebo-controlled, multicentre study. Plasma concentrations of ANP, BNP and cGMP were determined before randomization and after 21 days of treatment. In parallel with decreased pulmonary and systemic vascular resistance, 3 weeks of oral treatment with the ET(A) receptor antagonist darusentan reduced BNP plasma levels and increased the cGMP:BNP ratio significantly. The improved cGMP:BNP ratio might reflect the ability of chronic ET(A) receptor blockade to facilitate the generation of the second messenger cGMP, which points towards a favourable modulation of the natriuretic peptide effector system, in addition to haemodynamic improvement in heart failure patients.
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Philipp et al. (2002) conducted an RCT in chronic heart failure (n=142). darusentan vs. placebo was evaluated on Plasma concentrations of ANP, BNP and cGMP and cGMP:BNP ratio. Oral treatment with the ET(A) receptor antagonist darusentan for 21 days significantly reduced BNP plasma levels and increased the cGMP:BNP ratio in patients with chronic heart failure.
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