Key result
The SIGNIfY trial is designed to evaluate ivabradine for reducing cardiovascular mortality and hospitalization for myocardial infarction in CAD patients with resting heart rate ≥70 bpm.
Why the study?
Does ivabradine reduce cardiovascular mortality and hospitalization for myocardial infarction in patients with coronary artery disease and normal left ventricular function with a resting heart rate of ≥70 b.p.m.?
Does ivabradine reduce cardiovascular mortality and hospitalization for myocardial infarction in patients with coronary artery disease and normal left ventricular function with a resting heart rate of ≥70 b.p.m.?
The SIGNIfY trial is designed to evaluate whether heart rate reduction with ivabradine improves cardiovascular outcomes in patients with coronary artery disease and normal left ventricular function.
Recently, it has been recognized that elevated resting heart rate (HR) is an independent risk factor for all-cause and cardiovascular mortality, not only in the general population, but also in patients with cardiovascular disease. Ivabradine is a specific inhibitor of the If current in the sinoatrial node providing a pure HR reduction without modification of other cardiovascular parameters. Treatment with ivabradine therefore provides an opportunity to assess the effects of lowering HR without directly altering other aspects of cardiac function. Ivabradine has been proven to effectively prevent myocardial ischaemia and treat symptoms in patients with chronic stable angina pectoris. The BEAUTIfUL trial sheds new light on the role of HR control in cardiovascular disease and shows that ivabradine in patients with HR above 70 b.p.m. prevents coronary outcomes. These are particularly important data because they have been obtained on top of the best possible preventive therapy, including β-blockers. BEAUTIfUL has also led to a series of stimulating hypotheses that constitute the rationale for another trial called SIGNIfY, which will enrol patients with coronary artery disease (CAD) and normal left ventricular function with a resting HR of ≥70 b.p.m. The primary endpoint will take into consideration only CAD outcomes, i.e. CV mortality and hospitalization for myocardial infarction. So SIGNIfY will be a logical extension of BEAUTIfUL.
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Roberto Ferrari (2009) studied Coronary artery disease. Ivabradine was evaluated on CV mortality and hospitalization for myocardial infarction. The SIGNIfY trial is designed to evaluate ivabradine for reducing cardiovascular mortality and hospitalization for myocardial infarction in CAD patients with resting heart rate ≥70 bpm.
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