Abstract
Heart failure is a major burden on public health resources and the prevalence of the condition is rising as the population ages and with the increasing success of salvage strategies for myocardial infarction. The emphasis in management has changed over the last 20 years from the use of predominantly inotropic agents to drugs that regulate neurohumoral activity. This has reaped rewards in terms of improving reducing mortality but much remains to be done. Now, in common with the approach taken to other cardiovascular diseases, there is considerable interest in the use of genetic information to refine and personalize the treatment of heart failure, in the expectation that this will bring about further benefits to the patient and a more rational use of resources. The genetic information that may be of use in this respect is very wide ranging, encompassing factors that predispose to the disease (through atheroma, hypertension, resistance to oxidative damage, etc.), and genetic traits that influence prognosis, the ability to metabolize drugs and drug targets. This review will focus on studies in humans that have investigated the relationship between genotypes in candidate genes and susceptibility to heart failure, prognosis and response to treatment. In general these studies have been conducted on relatively small patient groups and as such have not yielded conclusive results which have changed clinical practice. Nonetheless, the studies provide encouragement and a basis for further investigations in larger, well-characterized populations.
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Stanton, T., Connell, J.M.C., McMurray, J.J.V. (2004). Genetic Determinants of Susceptibility, Prognosis and Treatment in Heart Failure. In: Wilkins, M.R. (eds) Cardiovascular Pharmacogenetics. Handbook of Experimental Pharmacology, vol 160. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-06214-2_8
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DOI: https://doi.org/10.1007/978-3-662-06214-2_8
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