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Aldosterone antagonism in addition to angiotensin-converting enzyme inhibitors in heart failure
1Medizinische Universitätsklinik, Würzburg, Germany. j.bauersachs@medizin.uni-wuerzburg.de
Insights
Aldosterone contributes to heart failure by promoting cardiac remodeling and fibrosis. Spironolactone, an aldosterone antagonist, significantly reduces mortality in heart failure patients, with eplerenone showing promise as a safer alternative.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- The systemic renin-angiotensin-aldosterone system's role in heart failure is established.
- A local cardiac aldosterone system's impact on heart failure is a recent discovery.
- Aldosterone exacerbates cardiac hypertrophy, fibrosis, and left ventricular remodeling in heart failure and post-myocardial infarction.
Purpose of the Study:
- To review the role of aldosterone in heart failure pathophysiology.
- To evaluate the efficacy of mineralocorticoid receptor antagonists like spironolactone and eplerenone in managing heart failure.
- To discuss the benefits and risks associated with aldosterone antagonism in heart failure treatment.
Main Methods:
- Review of existing literature, including landmark clinical trials like RALES.
- Analysis of aldosterone's effects on cardiac structure and function.
- Evaluation of clinical outcomes associated with aldosterone antagonist therapy.
Main Results:
- Plasma aldosterone levels correlate with worse prognosis in heart failure.
- ACE inhibitors provide only temporary reduction in aldosterone levels ('aldosterone escape').
- Spironolactone significantly reduces mortality and prevents heart failure worsening when added to ACE inhibitors.
- Spironolactone's benefits include reduced fibrosis, regression of hypertrophy, and improved endothelial function.
- Low-dose spironolactone in RALES showed minimal hyperkalemia risk, but broader use necessitates monitoring.
- Eplerenone, a more selective antagonist, is effective in hypertension and promising for heart failure.
Conclusions:
- Aldosterone plays a significant role in heart failure progression.
- Mineralocorticoid receptor antagonists, particularly spironolactone, are crucial in heart failure management.
- Careful monitoring of potassium and renal function is essential during aldosterone antagonist therapy.
- Eplerenone represents a potentially safer therapeutic option for heart failure.
Abstract:
Although the role of the systemic renin-angiotensin-aldosterone system in the pathophysiology of heart failure is well-known for years, the impact of a local cardiac aldosterone system has been recognized recently. Aldosterone promotes cardiac hypertrophy and fibrosis in hypertension and heart failure and is involved in left ventricular remodeling after myocardial infarction. Plasma aldosterone levels in patients with heart failure are an indicator of a worse prognosis. Although ACE inhibitor therapy in these patients reduces plasma aldosterone levels, this effect is only transitory, a phenomenon referred to as "aldosterone escape". Even maximally recommended doses of ACE inhibitors do not completely prevent ACE-mediated formation of angiotensin II in chronic heart failure, and those patients with increased aldosterone levels during ACE inhibition have impaired exercise capacity. The RALES study has demonstrated convincingly that in patients with heart failure, addition of the mineralocorticoid receptor antagonist spironolactone (25 mg/d) to ACE inhibition markedly reduces mortality and prevents worsening heart failure. While reduction of excessive extracellular matrix turnover leading to decreased fibrosis appears to be the most important effect of spironolactone in heart failure, other mechanisms such as regression of hypertrophy, improvement of endothelial function, enhanced renal sodium excretion and antiarrhythmic actions may contribute. In RALES, low-dose spironolactone did not confer a substantial risk of hyperkalemia, however, with broader use of spironolactone in heart failure, cases of hyperkalemia associated with the use of this drug increase. Close control of serum potassium and creatinine and estimation of creatinine clearance are mandatory, especially in the presence of additional factors impairing renal function. The new and more selective aldosterone antagonist eplerenone which is devoid of some side effects of spironolactone, has been shown to be effective in hypertension and holds great promise as future therapeutic agent in patients with heart failure.
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