Oral conjugated equine estrogen increases plasma von Willebrand factor in postmenopausal women

J Am Coll Cardiol. 2002 Dec 4;40(11):1991-9. doi: 10.1016/s0735-1097(02)02565-2.

Abstract

Objectives: We sought to test whether one month of daily oral conjugated equine estrogen (CEE) or transdermal estradiol alters hemostatic factors in postmenopausal subjects.

Background: Estrogen replacement therapy and hormonal replacement therapy (HRT) effect an early increase in cardiovascular events in postmenopausal women. Circulating plasma von Willebrand factor (vWF) antigen is a marker of generalized endothelial dysfunction and atherothrombosis.

Methods: Thirty-eight healthy postmenopausal women (average 59 +/- 7 years) were randomized to receive daily oral CEE, 0.625 mg (n = 21); transdermal estradiol, 0.1 mg/day (n = 7); or oral placebo (n = 10) for one month. Blood samples were collected at baseline and after two weeks and four weeks of therapy for measurement of circulating plasma hormones, lipid concentrations, and hemostatic factors.

Results: Oral CEE decreased total cholesterol (p < 0.01) and low-density lipoprotein cholesterol (p < 0.01), although it increased both triglycerides (p < 0.05) and high-density lipoprotein cholesterol (p < 0.01). Transdermal estradiol had no significant effect on lipids. Plasminogen activator inhibitor-1 antigen declined in both oral CEE and transdermal estradiol users, but did not achieve statistical significance. Fibrin D-dimer antigen did not vary significantly in any group. However, oral CEE users had a significant increase in vWF from baseline to four weeks (p < 0.03) and a decrease in tissue-type plasminogen activator antigen from baseline to four weeks (p < 0.004), which was significantly different from the change observed in the transdermal estradiol group (p < 0.05).

Conclusions: These data suggest that the oral CEE-mediated increase in plasma vWF may have clinical relevance given the early atherothrombotic effects of HRT in postmenopausal women.

Publication types

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

MeSH terms

  • Administration, Cutaneous
  • Administration, Oral
  • Aged
  • Biomarkers / blood
  • Cholesterol, HDL / blood
  • Cholesterol, HDL / drug effects
  • Cholesterol, LDL / blood
  • Cholesterol, LDL / drug effects
  • Double-Blind Method
  • Estradiol / administration & dosage
  • Estrogens, Conjugated (USP) / administration & dosage*
  • Female
  • Humans
  • Middle Aged
  • New York
  • Postmenopause / blood*
  • Postmenopause / drug effects*
  • Treatment Outcome
  • Triglycerides / blood
  • Women's Health
  • von Willebrand Factor / analysis*
  • von Willebrand Factor / drug effects

Substances

  • Biomarkers
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Estrogens, Conjugated (USP)
  • Triglycerides
  • von Willebrand Factor
  • Estradiol