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Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
Author(s) -
Neil A. Smart,
Nigel Kwok,
David J. Holland,
Rohan Jayasighe,
Francesco Giallauria
Publication year - 2011
Publication title -
clinical medicine insights cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.634
H-Index - 21
ISSN - 1179-5468
DOI - 10.4137/cmc.s4309
Subject(s) - sympatholytic , heart failure , medicine , pharmacogenomics , ejection fraction , cardiology , heart rate , clinical trial , beta blocker , blood pressure , pharmacology
Bucindolol is a non-selective β-adrenergic receptor blocker with α-1 blocker properties and mild intrinsic sympatholytic activity. The Beta-Blocker Evaluation of Survival Trial (BEST), which is the largest clinical trial of bucindolol in patients with heart failure, was terminated prematurely and failed to show an overall mortality benefit. However, benefits on cardiac mortality and re-hospitalization rates were observed in the BEST trial. Bucindolol has not shown benefits in African Americans, those with significantly low ejection fraction and those in NYHA class IV heart failure. These observations could be due to the exaggerated sympatholytic response to bucindolol in these sub-groups that may be mediated by genetic polymorphisms or changes in gene regulation due to advanced heart failure. This paper provides a timely clinical update on the use of bucindolol in chronic heart failure.

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