Key result
This review summarizes the most significant polymorphisms involving adrenergic receptors, related proteins, and genetic variations influencing beta-blocker metabolism in heart failure.
This review highlights the role of genetic polymorphisms in adrenergic receptors and related proteins in explaining the variable response to beta-blockers in heart failure patients.
May guide pharmacogenomic research on beta-blocker response in heart failure; leaves open prospective validation before clinical adoption.
Tailoring therapy for heart failure: the pharmacogenomics of adrenergic receptor signaling Grazia Daniela Femminella,1 Vincenzo Barrese,2,3 Nicola Ferrara,1,4 Giuseppe Rengo4 1Department of Translational Medical Sciences, Federico II University, Naples, Italy; 2Department of Neuroscience, Reproductive Science and Odontostomatology, Federico II University, Naples, Italy; 3Division of Biomedical Sciences, St George’s University of London, London, UK; 4”Salvatore Maugeri” Foundation – IRCCS – Scientific Institute of Telese Terme, Telese Terme, Benevento, Italy Abstract: Heart failure is one of the leading causes of mortality in Western countries, and β-blockers are a cornerstone of its treatment. However, the response to these drugs is variable among individuals, which might be explained, at least in part, by genetic differences. Pharmacogenomics is the study of genetic contributions to drug response variability in order to provide evidence for a tailored therapy in an individual patient. Several studies have investigated the pharmacogenomics of the adrenergic receptor system and its role in the context of the use of β-blockers in treating heart failure. In this review, we will focus on the most significant polymorphisms described in the literature involving adrenergic receptors and adrenergic receptor-related proteins, as well as genetic variations influencing β-blocker metabolism.
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Rengo et al. (2014) conducted a review in Heart failure. Pharmacogenomics of adrenergic receptor signaling and beta-blockers was evaluated. This review summarizes the most significant polymorphisms involving adrenergic receptors, related proteins, and genetic variations influencing beta-blocker metabolism in heart failure.
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