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Revista médica de Chile

versión impresa ISSN 0034-9887

Resumen

VERDUGO, Fernando J; MONTELLANO, Felipe A; CARRENO, Juan E  y  MARUSIC, Elisa T. Mineralocorticoid receptor antagonists and therapeutic strategies of cardiovascular damage. Rev. méd. Chile [online]. 2014, vol.142, n.1, pp.61-71. ISSN 0034-9887.  http://dx.doi.org/10.4067/S0034-98872014000100010.

In recent years, much attention has focused on the role of aldosterone and mineralocorticoid receptors (MRs) in the pathophysiology of hypertension and cardiovascular disease. Patients with primary aldosteronism, in whom angiotensin II levels are low, have a higher incidence of cardiovascular complications than patients with essential hypertension. The Randomized Aldactone Evaluation Study (RALES) demonstrated that adding a non-specific MR antagonist, spironolactone, to a standard therapy that included angiotensin-converting enzyme (ACE) inhibitors, loop diuretics, and digoxin, significantly reduced morbidity and mortality in patients with moderate to severe heart failure. Similarly, the Eplerenone Post-Acute Myocardial Infarction Heart Failure Efficacy and Survival Study (EPHESUS) showed that the addition of a selective MR antagonist (ARM), eplerenone, to an optimal medical therapy reduces morbidity and mortality among patients with acute myocardial infarction complicated by left ventricular dysfunction and heart failure. These data suggest that aldosterone induces cardiac injury through activation of MRs and support the notion that MR blockade has beneficial effects on aldosterone-dependent cardiac injury, through mechanisms that cannot be simply explained by hemodynamic changes. Although, MRA are highly effective in patients with heart failure, the risk of hyperkalemia should not be overlooked. Serious hyperkalemia events were reported in some MRA clinical trials; however these risks can be mitigated through appropriate patient selection, dose selection, patient education, monitoring, and follow-up.

Palabras clave : Aldosterone; Cardiovascular Diseases; Mineralocorticoid receptor antagonists; Spironolactone.

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