Raloxifene reduces procarboxypeptidase U, an antifibrinolytic marker. A 2-year randomized, placebo-controlled study in healthy early postmenopausal women

Menopause. 2004 Jan-Feb;11(1):110-5. doi: 10.1097/01.GME.0000097740.18446.77.

Abstract

Objective: The aim of this study was to compare the long-term effects of two dosages of raloxifene with oral hormone therapy (HT; conjugated equine estrogens combined with medroxyprogesterone acetate) on procarboxypeptidase U.

Design: In a randomized, double-blind, placebo-controlled, 2-year study, 95 healthy, nonhysterectomized, early postmenopausal women received either daily raloxifene 60 mg (n = 24), raloxifene 150 mg (n = 23), HT (conjugated equine estrogens 0.625 mg + medroxyprogesterone acetate 2.5 mg, n = 24), or placebo (n = 24). At baseline and after 6, 12, and 24 months, fasting plasma procarboxypeptidase U concentrations were measured.

Results: Six months of treatment with raloxifene 60 mg and raloxifene 150 mg were associated with significant decreases in plasma procarboxypeptidase U concentrations, which were sustained after 12 and 24 months. Raloxifene 60 mg: t = 0, 619 +/- 89 U/L (mean +/- SD); t = 6, 574 +/- 87 U/L; t = 12, 571 +/- 96 U/L; t = 24, 568 +/- 92 U/L; ANCOVA versus placebo, P = 0.026. Raloxifene 150 mg: t = 0, 608 +/- 67 U/L; t = 6, 580 +/- 73 U/L; t = 12, 578 +/- 70 U/L; t = 24, 562 +/- 61 U/L; ANCOVA versus placebo, P = 0.039. No significant changes were found in the HT group.

Conclusion: Long-term treatment with raloxifene reduced procarboxypeptidase U plasma concentrations.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Biomarkers / blood
  • Carboxypeptidase B2 / blood*
  • Contraceptive Agents, Female / pharmacology
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Estrogen Replacement Therapy
  • Estrogens / pharmacology
  • Estrogens, Conjugated (USP) / pharmacology
  • Female
  • Fibrinolysis*
  • Humans
  • Medroxyprogesterone Acetate / pharmacology
  • Middle Aged
  • Postmenopause / blood*
  • Raloxifene Hydrochloride / pharmacology*
  • Selective Estrogen Receptor Modulators / pharmacology*

Substances

  • Biomarkers
  • Contraceptive Agents, Female
  • Estrogens
  • Estrogens, Conjugated (USP)
  • Selective Estrogen Receptor Modulators
  • Raloxifene Hydrochloride
  • Medroxyprogesterone Acetate
  • Carboxypeptidase B2