Why the study?
NO-sGC-cGMP signalling is impaired in HF syndromes, and while nitrates stimulate cGMP, they are limited by tolerance, prompting exploration of alternative therapeutic targets to increase cGMP concentrations.
Do sGC stimulators and activators improve outcomes in patients with heart failure?
Do sGC stimulators and activators improve outcomes in patients with heart failure?
sGC stimulators and activators are emerging therapies for heart failure that target impaired NO-sGC-cGMP signaling, with vericiguat currently in phase III trials.
Vericiguat should not yet alter heart failure management; phase III trials leave open whether sGC stimulation improves outcomes.
Nitric oxide (NO)-soluble guanylate cyclase(sGC)-cGMP signalling is impaired in HF syndromes, which could predispose to vascular oxidative stress. Nitrates directly stimulate cGMP, but are limited by tolerance. Therapeutic targets that aim at increasing cGMP concentrations have therefore been explored. Recently, two classes of drugs have been discovered, the sGC activators and the sGC stimulators, which target two different redox states of sGC: the NO-sensitive reduced (ferrous) sGC and NO-insensitive oxidized (ferric) sGC, respectively. Cinaciguat is an activator and riociguat and vericiguat are sGC stimulators. Vericiguat is the most advanced agent in its clinical trial programme with two completed phase IIb studies, SOCRATES -REDUCED in HFrEF and SOCRATES-PRESERVED in HFpEF, with mixed results on NT-proBNP. The ongoing VICTORIA trial in HFrEF will study 4,872 participants with a mortality/morbidity end-point and VITALITY HFpEF trial will study 735 participants, with a quality of life end-point.
No takes yet. Share an insight, caveat, or question.
Tolppanen et al. (2019) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: