What are the symptoms and treatment options for hyperaldosteronism?

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Symptoms of Hyperaldosteronism

The majority of patients with hyperaldosteronism present with hypertension—often severe or resistant to treatment—while hypokalemia occurs in only approximately 50% of cases, making it an unreliable screening marker. 1, 2

Primary Clinical Manifestations

Hypertension

  • Severe, resistant hypertension is the hallmark presentation, defined as blood pressure not controlled on 3 or more medications including a diuretic 3, 1
  • Patients may present with accelerated or malignant hypertension, particularly with abrupt onset or loss of previously controlled blood pressure 3
  • Hypervolemia or normovolemia despite severe diastolic hypertension is characteristic in the majority of patients 4

Electrolyte Abnormalities

  • Hypokalemia is present in only 50% of patients with primary aldosteronism, so normal potassium does not exclude the diagnosis 1, 2
  • When present, hypokalemia may be spontaneous or diuretic-induced 2
  • Unprovoked or excessive hypokalemia (not taking a diuretic) should raise suspicion 3
  • Mild extracellular volume expansion occurs due to aldosterone-induced sodium retention in the distal convoluted tubule 1

Cardiovascular and Renal Manifestations

  • Prolonged aldosterone excess causes target organ damage to the heart, kidney, and arterial wall, resulting in increased cardiovascular morbidity and mortality beyond that explained by hypertension alone 5
  • Serum creatinine may be elevated, particularly in patients with severe hypertension and secondary kidney damage 1
  • In advanced cases, hypertensive kidney damage can cause renin to escape suppression, presenting with normal to high-normal renin levels 6

High-Risk Clinical Scenarios Warranting Screening

The following presentations should trigger screening for hyperaldosteronism 1, 2:

  • Resistant hypertension (BP uncontrolled on ≥3 drugs including a diuretic) - prevalence up to 20% 3, 1
  • Severe hypertension (BP >180/110 mmHg) 1
  • Hypertension with spontaneous or diuretic-induced hypokalemia 2
  • Incidentally discovered adrenal mass on imaging 1, 2
  • Early-onset hypertension (<30-40 years of age) or family history of early-onset hypertension 3, 1
  • Stroke at young age (<40 years) 1
  • Abrupt onset or abrupt loss of blood pressure control 3

Treatment Overview

Unilateral Disease

  • Laparoscopic unilateral adrenalectomy is the treatment of choice for unilateral aldosterone production, improving blood pressure in virtually 100% of patients and achieving complete cure of hypertension in approximately 50% 1, 2
  • Surgery normalizes hypokalemia, lowers blood pressure, reduces antihypertensive medication requirements, and improves cardiac and kidney function 1
  • Adrenal venous sampling is mandatory before surgery to distinguish unilateral from bilateral disease, except in patients <40 years with a single affected gland on imaging 1

Bilateral Disease

  • Mineralocorticoid receptor antagonists (MRAs) are the cornerstone of medical therapy for bilateral disease 1, 2
  • Spironolactone is first-line treatment, starting at 12.5-25 mg/day and titrating up to 100 mg/day as needed 7, 8
  • For primary hyperaldosteronism, doses of 100-400 mg daily may be used 7
  • Eplerenone (50-100 mg/day) is an alternative with fewer anti-androgenic side effects 1, 8
  • Close monitoring of serum potassium and creatinine is essential when initiating MRAs, particularly in patients with renal impairment (eGFR <45 mL/min/1.73 m²) 2, 8

Critical Treatment Considerations

  • Avoid combining MRAs with other potassium-sparing medications or potassium supplements due to hyperkalemia risk 2
  • In patients with advanced hypertensive kidney damage, spironolactone therapy may cause marked increases in serum creatinine and potassium 6
  • Additional antihypertensive agents (potassium-sparing diuretics like amiloride, or calcium channel blockers) may be necessary if blood pressure is not normalized with MRAs alone 8
  • The goal of treatment extends beyond blood pressure normalization to include correction of aldosterone excess and prevention of target organ damage 5

References

Guideline

Screening for Primary Aldosteronism

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Diagnosis and Treatment of Hyperaldosteronism

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Cardiovascular Risk in Primary Hyperaldosteronism.

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 2015

Research

Primary hyperaldosteronism without suppressed renin due to secondary hypertensive kidney damage.

The Journal of clinical endocrinology and metabolism, 2000

Research

Treatment of primary aldosteronism.

Best practice & research. Clinical endocrinology & metabolism, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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