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Updated: Oct 1, 2025

An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
Menopause-associated risk of cardiovascular disease
Panagiotis Anagnostis1, Irene Lambrinoudaki2, John C Stevenson3
1Unit of Reproductive Endocrinology, 1st Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Insights
Menopause increases cardiovascular disease (CVD) risk in women. Menopausal hormone therapy (MHT) can mitigate these risks, especially when started early, but is not recommended solely for CVD prevention.
Area of Science:
- Cardiology
- Endocrinology
- Women's Health
Background:
- Cardiovascular disease (CVD) is a significant concern for menopausal women due to hormonal changes.
- These changes contribute to risk factors like visceral obesity, dyslipidemia, glucose dysregulation, NAFLD, and hypertension.
- Early menopause (<45 years) is independently linked to increased CVD events.
Purpose of the Study:
- To evaluate the role of menopausal hormone therapy (MHT) in mitigating CVD risk factors in menopausal women.
- To assess the optimal timing and type of MHT for cardiovascular health.
- To clarify MHT's contraindications and its specific role in CVD prevention.
Main Methods:
- Review of existing literature on menopause, CVD risk factors, and menopausal hormone therapy.
- Analysis of the impact of different MHT formulations (transdermal estrogens, specific progestogens) on CVD risk markers.
- Examination of clinical guidelines regarding MHT initiation and contraindications.
Main Results:
- Menopausal hormone therapy (MHT) can improve key CVD risk factors.
- Transdermal estrogens are preferred due to no increase in triglycerides and lower VTE risk.
- MHT may reduce CVD morbidity and mortality if initiated early post-menopause (<60 years or within 10 years of LMP).
- MHT is crucial for women with premature ovarian insufficiency (POI) until average menopause age.
- MHT is contraindicated in women with a history of VTE.
- Breast cancer risk with MHT is generally low, influenced by progestogen type; micronized progesterone and dydrogesterone show lower risk.
Conclusions:
- MHT can effectively manage CVD risk factors associated with menopause.
- Early initiation of MHT in the postmenopausal period may offer cardiovascular benefits.
- MHT is not recommended solely for CVD prevention and has specific contraindications.
- The choice of progestogen in MHT influences breast cancer risk.
Abstract:
Cardiovascular disease (CVD) is of major concern in women entering menopause. The changing hormonal milieu predisposes them to increased CVD risk, due to a constellation of risk factors, such as visceral obesity, atherogenic dyslipidemia, dysregulation in glucose homeostasis, non-alcoholic fatty liver disease and arterial hypertension. However, an independent association of menopause per se with increased risk of CVD events has only been proven for early menopause (<45 years). Menopausal hormone therapy (MHT) ameliorates most of the CVD risk factors mentioned above. Transdermal estrogens are the preferable regimen, since they do not increase triglyceride concentrations and they are not associated with increased risk of venous thromboembolic events (VTE). Although administration of MHT should be considered on an individual basis, MHT may reduce CVD morbidity and mortality, if commenced during the early postmenopausal period (<60 years or within ten years since the last menstrual period). In women with premature ovarian insufficiency (POI), MHT should be administered at least until the average age of menopause (50-52 years). MHT is contraindicated in women with a history of VTE and is not currently recommended for the sole purpose of CVD prevention. The risk of breast cancer associated with MHT is generally low and is mainly conferred by the progestogen. Micronized progesterone and dydrogesterone are associated with lower risk compared to other progestogens.
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