Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY?
An elevated heart rate is a marker of cardiovascular risk in patients with stable coronary artery disease. Ivabradine selectively inhibits the “f” current in the sinus node and reduces heart rate without any modifications of blood pressure, myocardial contractility and arteriolar resistance. However...
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doaj-100708e70fb44a54a29ae5ea89099cc02020-11-24T22:35:52ZengElsevierContemporary Clinical Trials Communications2451-86542016-12-014C586310.1016/j.conctc.2016.06.003Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY?Gian Piero Perna0Fabio Vagnarelli1Maurizio Volterrani2Ilaria Battistoni3Claudio Rapezzi4Cardiology, Cardiovascular Department, “Ospedali Riuniti di Ancona”, Ancona, ItalyCardiology, Department of Experimental Diagnostic and Specialty Medicine, Alma Mater Studiorum-University of Bologna, Bologna, ItalyCardiology, “San Raffaele Hospital”, Roma, ItalyCardiology, Cardiovascular Department, “Ospedali Riuniti di Ancona”, Ancona, ItalyCardiology, Department of Experimental Diagnostic and Specialty Medicine, Alma Mater Studiorum-University of Bologna, Bologna, ItalyAn elevated heart rate is a marker of cardiovascular risk in patients with stable coronary artery disease. Ivabradine selectively inhibits the “f” current in the sinus node and reduces heart rate without any modifications of blood pressure, myocardial contractility and arteriolar resistance. However the addition of ivabradine to standard therapy to reduce heart rate did not improve outcomes in the recent SIGNIFY trial. Moreover, a significant interaction between the effect of ivabradine among subgroups with and without angina was detected, with a worse outcome in patients in CCS class >II at baseline. The explanation for this surprising finding despite a significant reduction in angina and myocardial revascularization procedures is uncertain. A J-curve for heart rate was not demonstrated. We speculate a significant interference on adverse events (mainly atrial fibrillation and consequently acute coronary syndromes) and on the outcome of unfavorable interactions between ivabradine and diltiazem, verapamil and strong inhibitors of CYP3A4 (4.6% of the total population). Indeed, when these patients are excluded from subgroup analysis, the harmful effect of Ivabradine among patients with severe angina disappears. In conclusion, heart rate is a marker of risk but is not a risk factor and/or a target of therapy in patients with stable coronary artery disease and preserved ventricular systolic function. Standard doses of ivabradine are indicated for treatment of angina as an alternative or in addition to beta-blockers, but should not be administered in association with CYP3A4 inhibitors or heart rate-lowering calcium-channel blockers.http://www.sciencedirect.com/science/article/pii/S2451865415300247 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Gian Piero Perna Fabio Vagnarelli Maurizio Volterrani Ilaria Battistoni Claudio Rapezzi |
spellingShingle |
Gian Piero Perna Fabio Vagnarelli Maurizio Volterrani Ilaria Battistoni Claudio Rapezzi Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? Contemporary Clinical Trials Communications |
author_facet |
Gian Piero Perna Fabio Vagnarelli Maurizio Volterrani Ilaria Battistoni Claudio Rapezzi |
author_sort |
Gian Piero Perna |
title |
Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? |
title_short |
Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? |
title_full |
Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? |
title_fullStr |
Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? |
title_full_unstemmed |
Heart rate modulation in stable coronary artery disease without clinical heart failure: What we have already learned from SIGNIFY? |
title_sort |
heart rate modulation in stable coronary artery disease without clinical heart failure: what we have already learned from signify? |
publisher |
Elsevier |
series |
Contemporary Clinical Trials Communications |
issn |
2451-8654 |
publishDate |
2016-12-01 |
description |
An elevated heart rate is a marker of cardiovascular risk in patients with stable coronary artery disease. Ivabradine selectively inhibits the “f” current in the sinus node and reduces heart rate without any modifications of blood pressure, myocardial contractility and arteriolar resistance. However the addition of ivabradine to standard therapy to reduce heart rate did not improve outcomes in the recent SIGNIFY trial. Moreover, a significant interaction between the effect of ivabradine among subgroups with and without angina was detected, with a worse outcome in patients in CCS class >II at baseline. The explanation for this surprising finding despite a significant reduction in angina and myocardial revascularization procedures is uncertain. A J-curve for heart rate was not demonstrated. We speculate a significant interference on adverse events (mainly atrial fibrillation and consequently acute coronary syndromes) and on the outcome of unfavorable interactions between ivabradine and diltiazem, verapamil and strong inhibitors of CYP3A4 (4.6% of the total population).
Indeed, when these patients are excluded from subgroup analysis, the harmful effect of Ivabradine among patients with severe angina disappears.
In conclusion, heart rate is a marker of risk but is not a risk factor and/or a target of therapy in patients with stable coronary artery disease and preserved ventricular systolic function. Standard doses of ivabradine are indicated for treatment of angina as an alternative or in addition to beta-blockers, but should not be administered in association with CYP3A4 inhibitors or heart rate-lowering calcium-channel blockers. |
url |
http://www.sciencedirect.com/science/article/pii/S2451865415300247 |
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