Administration of raloxifene does not influence 24-hour ambulatory blood pressure of postmenopausal women with osteopenia: a double-blind placebo-controlled study

Am J Obstet Gynecol. 2003 May;188(5):1278-82. doi: 10.1067/mob.2003.299.

Abstract

Objective: Because estrogens may decrease 24-hour blood pressure of postmenopausal women, we tested the effect of the selective estrogen receptor modulator raloxifene on ambulatory blood pressure.

Study design: Postmenopausal women with osteopenia who were otherwise healthy were assigned randomly in a double blind-fashion to receive placebo (n = 16 women) or raloxifene (60 mg/d, n = 16 women). Before and after 4 months, the blood pressure of each woman was monitored every 30 minutes for 41 hours with the use of an ambulatory device.

Results: Similar to the placebo outcome, the raloxifene administration did not modify 24-hour daytime (7 AM -11 PM) and nighttime (11 PM -7 AM) blood pressure and heart rate values. Day-night differences and the 24-hour rhythmic variation of mean blood pressure, which was evaluated by cosinor analysis, were also not affected by placebo or by raloxifene.

Conclusion: Raloxifene does not influence 24-hour blood pressure of postmenopausal women. These data are reassuring for the cardiovascular safety of the long-term raloxifene administration.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Blood Pressure / drug effects
  • Blood Pressure Monitoring, Ambulatory*
  • Circadian Rhythm
  • Double-Blind Method
  • Female
  • Heart Rate / drug effects
  • Humans
  • Middle Aged
  • Osteoporosis, Postmenopausal / drug therapy
  • Osteoporosis, Postmenopausal / physiopathology*
  • Placebos
  • Raloxifene Hydrochloride / administration & dosage*
  • Selective Estrogen Receptor Modulators / administration & dosage*

Substances

  • Placebos
  • Selective Estrogen Receptor Modulators
  • Raloxifene Hydrochloride