Treatment of postmenopausal hypertension with moxonidine, a selective imidazoline receptor agonist

Int J Clin Pract Suppl. 2004 Mar:(139):26-32.

Abstract

This study compared the effects of two sympatholytic agents--one central (moxonidine) and one peripheral (atenolol)--on blood pressure and other metabolic syndrome factors in postmenopausal hypertensive women who were not taking hormone replacement therapy. Atenolol and moxonidine led to a statistically significant reduction in diastolic blood pressure of 9.5 mmHg and 5.5 mmHg, respectively. A clear rebound effect was observed in the atenolol patients whereas the moxonidine group exhibited a slightly further decrease in blood pressure. Moxonidine also caused a profound decrease in both mean plasma-glucose area under the curve (AUC) during oral glucose tolerance test (-0.96 mmol/L x H, NS) and mean plasma-insulin AUC (-6.15 mU/L x H). Therefore, moxonidine displayed a slightly less potent antihypertensive effect than atenolol in hypertensive postmenopausal women, but it demonstrated a better metabolic effect. To conclude, moxonidine could benefit hypertensive postmenopausal women who display other signs of metabolic syndrome.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antihypertensive Agents / therapeutic use*
  • Atenolol / therapeutic use*
  • Blood Glucose / analysis
  • Double-Blind Method
  • Female
  • Humans
  • Hypertension / drug therapy*
  • Hypertension / metabolism
  • Imidazoles / therapeutic use*
  • Imidazoline Receptors
  • Insulin / blood
  • Middle Aged
  • Postmenopause*
  • Prospective Studies
  • Receptors, Drug / metabolism
  • Sympatholytics / therapeutic use

Substances

  • Antihypertensive Agents
  • Blood Glucose
  • Imidazoles
  • Imidazoline Receptors
  • Insulin
  • Receptors, Drug
  • Sympatholytics
  • Atenolol
  • moxonidine