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An association between mineral metabolism and the renin-aldosterone system in human hypertension

L Lind1, L Wide, O H Sörensen

  • 1Department of Internal Medicine, Uppsala University, Sweden.

Insights

Essential hypertension may involve calcium metabolism disruptions. This study found serum magnesium and urinary calcium/cAMP correlate with renin-aldosterone markers, suggesting a link in hypertension.

Area of Science:

  • Nephrology
  • Endocrinology
  • Cardiovascular Medicine

Background:

  • Abnormalities in calcium metabolism are increasingly recognized in human hypertension.
  • The interplay between calcium homeostasis and the renin-aldosterone system in hypertension requires further elucidation.

Purpose of the Study:

  • To investigate the relationships between key indices of calcium metabolism and the renin-aldosterone system in untreated essential hypertension.
  • To determine if alterations in calcium balance are associated with the activity of the renin-aldosterone system in hypertensive individuals.

Main Methods:

  • Study included 39 subjects with untreated essential hypertension.
  • Measurements included plasma ionized calcium, parathyroid hormone, 1,25(OH)2-vitamin D, serum magnesium, plasma renin activity (PRA), and urinary aldosterone.
  • 24-hour urinary excretion of calcium and cyclic AMP (cAMP) were also assessed.

Main Results:

  • No significant associations were found between major calcium determinants (ionized calcium, PTH, 1,25(OH)2-vitamin D) and the renin-aldosterone system.
  • Serum magnesium showed a positive correlation with plasma renin activity (PRA).
  • Both 24-hour urinary calcium and cAMP excretion were positively correlated with PRA and urinary aldosterone.

Conclusions:

  • The renin-aldosterone system does not appear to significantly influence major determinants of calcium balance in human hypertension.
  • A 'urinary leak' of calcium may be influenced by the activity of the renin-aldosterone system in essential hypertension.
  • Serum magnesium and urinary calcium/cAMP warrant further investigation in the context of hypertension and mineralocorticoid activity.

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