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Updated: Jul 18, 2026

An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
[Menopausal hormone therapy and cardiovascular disease]
1Emory University School of Medicine, Grady Memorial Hospital, Emory Heart and Vascular Center, Atlanta, Georgia, USA. nwenger@emory.edu
Menopausal hormone therapy and SERMs did not prevent cardiovascular events in women. Aggressive cardiovascular risk reduction strategies are essential for menopausal women with heart disease.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Women's Health
Background:
- Observational studies suggested cardiovascular benefits of menopausal hormone therapy (MHT).
- Randomized clinical trials (RCTs) have yielded conflicting results regarding MHT's cardiovascular effects.
- Selective estrogen receptor modulators (SERMs) also showed no cardiovascular benefit in trials.
Purpose of the Study:
- To evaluate the efficacy of MHT and SERMs in preventing cardiovascular events in women.
- To determine if earlier initiation or different formulations of MHT could alter cardiovascular outcomes.
- To emphasize the need for established cardiovascular risk reduction strategies in menopausal women.
Main Methods:
- Analysis of data from well-designed randomized clinical trials.
- Inclusion of trials involving healthy women and those with established coronary heart disease.
- Review of trials evaluating MHT and the SERM raloxifene.
Main Results:
- MHT failed to prevent clinical cardiovascular events in RCTs and was associated with harm.
- Raloxifene did not decrease coronary events.
- Participants in trials often had suboptimal control of cardiovascular risk factors at baseline.
Conclusions:
- Current evidence does not support the use of MHT or SERMs for primary or secondary cardiovascular prevention in postmenopausal women.
- Optimal management of cardiovascular risk factors is crucial for menopausal women.
- Further research is needed to explore potential benefits of alternative MHT strategies (e.g., earlier initiation, lower doses, different routes).
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