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Serum and urinary magnesium during treatment of patients with chronic congestive heart failure

O O Oladapo1, A O Falase

  • 1Department of Anatomy, College of Medicine, University of Ibadan, Nigeria.

Insights

Congestive Heart Failure (CHF) patients exhibit higher urinary magnesium loss. Lisinopril treatment in CHF patients helps conserve magnesium, unlike other common medications.

Area of Science:

  • Cardiology
  • Nephrology
  • Clinical Pharmacology

Background:

  • Electrolyte disturbances are prevalent in Congestive Heart Failure (CHF) patients, particularly with long-term therapies.
  • The impact of CHF and its treatments on magnesium levels remains less understood compared to potassium.
  • Common CHF medications like diuretics can influence electrolyte balance.

Purpose of the Study:

  • To investigate serum and urinary magnesium concentrations in patients with Congestive Heart Failure (CHF).
  • To evaluate the effects of lisinopril (ACE inhibitor), frusemide (diuretic), and digoxin on magnesium levels over 4 weeks.
  • To compare magnesium levels in CHF patients with healthy controls.

Main Methods:

  • A cohort of 45 CHF patients (NYHA Class II-III) and 45 matched healthy controls were studied.
  • Serum and urinary magnesium were measured using atomic absorption spectrophotometry at baseline, 2 weeks, and 4 weeks.
  • Statistical analysis was performed using the Student's t-test.

Main Results:

  • Baseline serum magnesium was not significantly different between CHF patients and controls.
  • CHF patients showed significantly higher urinary magnesium excretion at baseline (p < 0.01).
  • Serum magnesium decreased significantly during treatment in most CHF patients, except for those on lisinopril.
  • Lisinopril-treated CHF patients exhibited the lowest magnesium excretion.

Conclusions:

  • Congestive Heart Failure patients experience increased urinary magnesium loss.
  • Lisinopril demonstrates a magnesium-sparing effect in CHF patients.
  • This suggests a beneficial role for lisinopril in maintaining magnesium homeostasis during CHF treatment.

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