[Cardiovascular risk and hormone replacement therapy in menopause]
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Updated: Oct 19, 2026

An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
1Hôpital Necker, Service Endocrinologie-Médecine de la Reproduction, Paris, France.
Insights
Hormone replacement therapy (HRT) reduces heart attack risk but increases stroke risk. Studies show mixed cardiovascular effects, with oral conjugated equine estrogen plus medroxyprogesterone acetate increasing thromboembolic events.
Area of Science:
- Cardiovascular epidemiology
- Hormone therapy research
- Clinical trial analysis
Context:
- Cardiovascular risk associated with hormone replacement therapy (HRT) varies by vessel type and location.
- Previous meta-analyses indicated HRT reduces ischemic heart disease and cardiovascular mortality.
- Recent studies highlight increased cerebrovascular risk, specifically ischemic stroke.
Purpose:
- To analyze the cardiovascular risk associated with different types of hormone replacement therapy (HRT).
- To synthesize findings on HRT's impact on ischemic heart disease, cardiovascular mortality, and stroke.
- To evaluate recent clinical trial data on HRT and cardiovascular outcomes.
Summary:
- HRT shows a 30-50% decrease in ischemic heart disease and a 25% decrease in cardiovascular mortality.
- HRT is associated with a 20% increase in ischemic stroke but a 30% protective effect in hemorrhagic stroke.
- A trial of oral conjugated equine estrogen plus medroxyprogesterone acetate showed no reduction in myocardial infarction or cardiovascular death and increased thromboembolic events.
Impact:
- Findings underscore the complex and site-specific effects of HRT on cardiovascular health.
- Highlights the need for further research on HRT formulations, particularly those used outside Anglo-Saxon countries.
- Emphasizes the unknown cardiovascular effects of transdermal estrogen with natural progesterone, commonly used in France.
Abstract:
Cardiovascular risk associated with hormone replacement therapy (HRT) has been analysed by large epidemiological studies. This treatment has different effects depending on the type of vessel (venous or arterial) or site (heart or brain). The several meta-analyses which have been published conclude that there is a significant decrease of about 30 to 50 per cent in ischaemic heart disease associated with HRT. In addition, oestrogen replacement therapy is associated with a 25 per cent decrease in cardiovascular mortality. A recent meta-analysis has analysed the effect of HRT on cerebrovascular risk. A significant 20 per cent increase in ischaemic stroke associated with the use of HRT has been shown. However, a protective association of about 30 per cent has been observed in haemorrhagic stroke with HRT use. Recent epidemiological studies have suggested an increased risk of thromboembolic disease associated with HRT. The results of a randomized blind placebo-controlled secondary prevention trial have recently been published. In this clinical trial, women who receive oestrogen (0.625 mg conjugated equine oestrogen daily) plus progestin (2.5 mg medroxyprogesterone acetate daily) therapy did not experience a reduction in overall risk of non-fatal myocardial infarction and cardiovascular heart disease death. This treatment also significantly increases the rate of thromboembolic events. Other randomized trials of HRT for primary prevention are scheduled to yield results by 2000 or 2005. All these studies have been conducted essentially in Anglo-Saxon countries and have analysed the effects of conjugated equine oestrogens alone or combined with medroxyprogesterone acetate. This treatment is not currently used in France. But no randomized trials are under way with the HRT common in France (transdermic oestrogen combined with natural progesterone). The effects of this treatment on cardiovascular disease remain unknown.
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