Key result
Nebivolol and metoprolol failed to prevent tachycardia-induced cardiomyopathy in a porcine model, with LVEF decreasing by 34%, 20%, and 20% in the nebivolol, metoprolol, and placebo groups.
Why the study?
Does nebivolol or metoprolol prevent tachycardia-induced cardiomyopathy in a porcine model?
RCT (n=15)
randomly assigned
Does nebivolol or metoprolol prevent tachycardia-induced cardiomyopathy in a porcine model?
In a porcine model of persistent tachycardia, neither nebivolol nor metoprolol prevented the development of tachycardia-induced cardiomyopathy compared to placebo.
Answers are grounded in this paper and cite their sources.
Does not support beta-blockers to prevent tachycardia cardiomyopathy in pigs; leaves open human translation.
Chronic tachycardia is a well-known cause of nonischemic cardiomyopathy. We hypothesized that nebivolol, a β-blocker with nitric oxide activity, would be superior to a pure β-blocker in preventing tachycardia-induced cardiomyopathy in a porcine model. Fifteen healthy Yucatan pigs were randomly assigned to receive nebivolol, metoprolol, or placebo once a day. All pigs underwent dual-chamber pacemaker implantation. The medication was started the day after the pacemaker implantation. On day 7 after implantation, each pacemaker was set at atrioventricular pace (rate, 170 beats/min), and the pigs were observed for another 7 weeks. Transthoracic echocardiograms, serum catecholamine levels, and blood chemistry data were obtained at baseline and at the end of the study. At the end of week 8, the pigs were euthanized, and complete histopathologic studies were performed. All the pigs developed left ventricular cardiomyopathy but remained hemodynamically stable and survived to the end of the study. The mean left ventricular ejection fraction decreased from baseline by 34%, 20%, and 20% in the nebivolol, metoprolol, and placebo groups, respectively. These changes did not differ significantly among the 3 groups ( P =0.51). Histopathologic analysis revealed mild left ventricular perivascular fibrosis with cardiomyocyte hypertrophy in 14 of the 15 pigs. Both nebivolol and metoprolol failed to prevent cardiomyopathy in our animal model of persistent tachycardia and a high catecholamine state.
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Nazeri et al. (2016) conducted an RCT in tachycardia-induced cardiomyopathy (n=15). nebivolol vs. metoprolol or placebo was evaluated on decrease in mean left ventricular ejection fraction from baseline (p=0.51). Nebivolol and metoprolol failed to prevent tachycardia-induced cardiomyopathy in a porcine model, with LVEF decreasing by 34%, 20%, and 20% in the nebivolol, metoprolol, and placebo groups.
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