Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure

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 fa...

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Main Authors: Neil A. Smart, Nigel Kwok, David J. Holland, Rohan Jayasighe, Francesco Giallauria
Format: Article
Language:English
Published: SAGE Publishing 2011-01-01
Series:Clinical Medicine Insights: Cardiology
Online Access:https://doi.org/10.4137/CMC.S4309
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spelling doaj-fee7be686cb34663bb202a1062d8d06b2020-11-25T03:12:24ZengSAGE PublishingClinical Medicine Insights: Cardiology1179-54682011-01-01510.4137/CMC.S4309Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart FailureNeil A. Smart0Nigel Kwok1David J. Holland2Rohan Jayasighe3Francesco Giallauria4School of Science and Technology, University of New England, Armidale, NSw 2351, Australia.School of Science and Technology, University of New England, Armidale, NSw 2351, Australia.The School of Science and Technology, University of New England, Armidale, NSw 2351, Australia.Comprehensive Heart Failure Service, Gold Coast Hospital / Griffith University, Australia.Department of Clinical Medicine, Cardiovascular and Immunological Sciences, Cardiac rehabilitation Unit, University of Naples “Federico II”.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.https://doi.org/10.4137/CMC.S4309
collection DOAJ
language English
format Article
sources DOAJ
author Neil A. Smart
Nigel Kwok
David J. Holland
Rohan Jayasighe
Francesco Giallauria
spellingShingle Neil A. Smart
Nigel Kwok
David J. Holland
Rohan Jayasighe
Francesco Giallauria
Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
Clinical Medicine Insights: Cardiology
author_facet Neil A. Smart
Nigel Kwok
David J. Holland
Rohan Jayasighe
Francesco Giallauria
author_sort Neil A. Smart
title Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
title_short Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
title_full Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
title_fullStr Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
title_full_unstemmed Bucindolol: A Pharmacogenomic Perspective on its Use in Chronic Heart Failure
title_sort bucindolol: a pharmacogenomic perspective on its use in chronic heart failure
publisher SAGE Publishing
series Clinical Medicine Insights: Cardiology
issn 1179-5468
publishDate 2011-01-01
description 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.
url https://doi.org/10.4137/CMC.S4309
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