Key result
Piboserod significantly increased LVEF by 1.7% vs. placebo (95% CI 0.3-3.2, P=0.020) in patients with chronic heart failure, though clinical relevance remains uncertain.
Why the study?
Does piboserod improve LVEF in patients with symptomatic heart failure and LVEF ≤0.35?
RCT (n=137)
Double-blind
parallel group
Does piboserod improve LVEF in patients with symptomatic heart failure and LVEF ≤0.35?
Piboserod treatment for 24 weeks resulted in a small but significant improvement in LVEF in patients with chronic heart failure, but without improvements in other clinical or biomarker parameters, leaving its clinical relevance uncertain.
AIMS: Myocardial 5-HT(4) serotonin (5-HT) receptors are increased and activated in heart failure (HF). Blockade of 5-HT(4) receptors reduced left ventricular (LV) remodelling in HF rats. We evaluated the effect of piboserod, a potent, selective, 5-HT(4) serotonin receptor antagonist, on LV function in patients with HF. METHODS AND RESULTS: This was a prospective, double-blind, parallel group trial in patients with NYHA class II-IV HF and LV ejection fraction (EF) < or =0.35. Patients receiving standard HF treatment were randomized to placebo (n = 70) or piboserod 80 mg (n = 67) for 24 weeks including 4 weeks up titration. The primary endpoint was LVEF measured by cardiac magnetic resonance imaging (MRI). Secondary endpoints were LV volumes, N-terminal pro-brain natriuretic peptide, norepinephrine, quality of life, and 6 min walk test. Piboserod significantly increased LVEF by 1.7% vs. placebo (CI 0.3, 3.2, P = 0.020), primarily through reduced end-systolic volume from 165 to 158 mL (P = 0.060). There was a trend for greater increase in LVEF (2.7%, CI -1.1, 6.6, P = 0.15) in a small subset of patients not on chronic beta-blocker therapy. There was no significant effect on neurohormones, quality of life, or exercise tolerance. Patients on piboserod reported more adverse events, but numbers were too small to identify specific safety issues. CONCLUSION: Although patients with chronic HF had a small but significant improvement in LVEF when treated with piboserod for 24 weeks, the result was not reflected in significant changes in other efficacy parameters, and its clinical relevance remains uncertain.
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Kjekshus et al. (2009) conducted an RCT in Symptomatic Heart Failure (n=137). Piboserod vs. Placebo was evaluated on LVEF measured by cardiac magnetic resonance imaging (MRI) (MD 1.7%, 95% CI 0.3, 3.2, p=0.020). Piboserod significantly increased LVEF by 1.7% vs. placebo (95% CI 0.3-3.2, P=0.020) in patients with chronic heart failure, though clinical relevance remains uncertain.
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