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Published on: September 26, 2018
Aldosterone and cardiovascular risk
Insights
Excess aldosterone contributes to hypertension and cardiovascular risk, potentially independent of blood pressure. Aldosterone receptor blockade shows promise for reducing cardiovascular and renal complications, warranting further trials.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Nephrology
Background:
- Aldosterone excess is linked to hypertension and increased cardiovascular and renal risk.
- Emerging evidence suggests aldosterone may independently elevate cardiovascular risk beyond its effects on blood pressure.
- Aldosterone is associated with obesity, metabolic syndrome, inflammation, oxidative stress, and fibrosis.
Purpose of the Study:
- To review the role of aldosterone in cardiovascular and renal risk.
- To explore the potential benefits of aldosterone receptor blockade.
Main Methods:
- Review of experimental and epidemiologic data.
- Analysis of clinical evidence from primary hyperaldosteronism and essential hypertension patients.
- Examination of studies on aldosterone receptor blockade effects.
Main Results:
- Primary hyperaldosteronism patients face higher cardiovascular and renal complication risks than essential hypertension patients with similar blood pressure.
- Aldosterone receptor blockade has demonstrated reductions in cardiovascular mortality post-myocardial infarction and in heart failure.
- Aldosterone blockade may positively influence chronic kidney disease progression.
Conclusions:
- Aldosterone plays a significant role in cardiovascular and renal pathology, potentially independent of its hypertensive effects.
- Aldosterone receptor blockade is a promising therapeutic strategy for mitigating cardiovascular and renal risks.
- Further prospective interventional trials are essential to confirm the benefits of aldosterone blockade on cardiovascular risk.
Abstract:
Through its classic effects on sodium and potassium homeostasis, aldosterone, when produced in excess, is associated with the development of hypertension and hence with higher cardiovascular and renal risk. In recent years, experimental and epidemiologic data have suggested that aldosterone also may be linked to high cardiovascular risk independently of its effects on blood pressure. Thus, aldosterone has been associated with obesity and metabolic syndrome in selected populations, and these associations may further contribute to the higher cardiovascular risk of subjects with elevated aldosterone levels. Moreover, aldosterone has been reported to promote inflammation, oxidative stress, and fibrosis in a number of tissues. Clinical evidence indicates that patients with primary hyperaldosteronism have a higher risk of developing cardiovascular and renal complications than patients with essential hypertension who have the same level of blood pressure. Aldosterone receptor blockade has been shown to lower cardiovascular mortality after myocardial infarction and in patients with congestive heart failure. Some studies have also demonstrated that aldosterone blockade could have a favorable impact on the progression of renal disease. However, prospective interventional trials are needed to further evaluate the impact of blockade of aldosterone on cardiovascular risk.
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