Estrogen OptimizationrctRCT2002

A placebo-controlled trial of long-term oral combined continuous hormone replacement therapy in postmenopausal women: effects on arterial compliance and endothelial function.

Clinical endocrinology

confidence

Key findings

Long-term combined HRT reduced Lp(a) but did not improve arterial compliance, PWV, or endothelial function vs placebo.

View source on PubMed (PMID 11894980) ↗

Sample size
59
Population
Healthy postmenopausal women
Dosing
Oestradiol 2 mg + norethisterone 1 mg (Kliogest), combined continuous
Duration
2 years (24 months)
Route
oral
Blinding
double_blind
Controls
placebo
Drug class
estrogen therapy

Measured endpoints

  • Lipoprotein a [Lp(a)]Decreasedmetabolic
    significant
  • Lipid profile (other than Lp(a))No changemetabolic
    not_significant
  • Systemic arterial compliance (SAC)No changecardiovascular
    not_significant
  • Pulse wave velocity (PWV)No changecardiovascular
    not_significant
  • Flow-mediated vasodilation (FMD)No changecardiovascular
    not_significant
Full abstract

To study the effects of long-term combined continuous oral hormone replacement therapy (HRT) on vascular function in healthy postmenopausal women. The cardiovascular effects of HRT are controversial. Improvement in vascular function is a proposed mechanism of oestrogen action but there are no long-term controlled human trials in this area. In this study, we examined the effects of HRT on lipid profiles and vascular function, encompassing both biomechanical arterial properties [systemic arterial compliance (SAC) and pulse wave velocity (PWV)] and endothelial function [flow-mediated vasodilation (FMD)]. In this 2-year, double-blind, placebo-controlled study, 59 healthy postmenopausal women were randomized to oral combined continuous oestrogen and progesterone [Kliogest, oestradiol (2 mg), norethisterone (1 mg)] or placebo, with end-points measured at baseline, 6 weeks and after 6,12 and 24 months of treatment. Oral combined HRT reduced lipoprotein a [Lp(a)], although other lipid benefits were not observed. There were no significant changes in SAC, PWV or FMD with oral combined HRT, compared to placebo. In this long-term, randomized placebo-controlled trial, oral continuous HRT with combined oestradiol and norethisterone in healthy postmenopausal women did not improve a spectrum of indices of arterial function compared to placebo. These results suggest that HRT might not be of cardiovascular benefit in postmenopausal women.

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