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Calcium antagonism in essential hypertension: effect on renal haemodynamics and microalbuminuria

B Persson1, O K Andersson, M Wysocki

  • 1Department of Medicine, Sahlgren's Hospital, University of Gothenburg, Sweden.

Insights

This study found that isradipine, a calcium antagonist, effectively lowers blood pressure in hypertensive men by reducing peripheral resistance. However, it did not significantly alter urinary albumin excretion rates.

Area of Science:

  • Cardiology
  • Nephrology
  • Pharmacology

Background:

  • Primary hypertension is a significant risk factor for cardiovascular and renal disease.
  • Urinary albumin excretion rate (UAE) is a marker of kidney damage and cardiovascular risk.
  • Calcium antagonists are a class of antihypertensive drugs with varying effects on renal parameters.

Purpose of the Study:

  • To investigate the effects of the calcium antagonist isradipine on blood pressure, systemic and renal hemodynamics, hemorheological properties, and urinary albumin excretion in men with primary hypertension.

Main Methods:

  • A randomized, placebo-controlled, double-blind cross-over study involving 16 middle-aged men with primary hypertension.
  • Treatment with isradipine over a 9-week period.
  • Assessment of urinary albumin excretion rate, systemic and renal hemodynamics, hemorheological properties, and plasma hormone/renin activity.

Main Results:

  • Isradipine significantly reduced blood pressure by decreasing peripheral resistance.
  • No significant influence of isradipine treatment on the mean urinary albumin excretion rate was observed.
  • Multivariate analysis indicated that changes in urinary albumin excretion were solely related to blood pressure changes.

Conclusions:

  • Isradipine is effective in lowering blood pressure in hypertensive men through reduced peripheral resistance.
  • Isradipine does not appear to directly impact urinary albumin excretion in this hypertensive cohort.
  • Blood pressure reduction is the primary determinant of changes in urinary albumin excretion in the context of isradipine treatment.

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