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Published on: August 13, 2019
Cardiovascular health and aromatase inhibitors
Kathleen I Pritchard1, Beth L Abramson
1Toronto-Sunnybrook Regional Cancer Centre, Sunnybrook Health Sciences Centre, and the University of Toronto, Toronto, Ontario, Canada. kathy.pritchard@sunnybrook.ca
Insights
Cardiovascular disease is a major concern for breast cancer patients. Aromatase inhibitors (AIs) do not increase cardiovascular risk, unlike tamoxifen which may increase thromboembolic events.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Cardiovascular disease (CVD) is the leading cause of death in North American women.
- CVD mortality is not uncommon in breast cancer patients due to shared risk factors and treatment complexities.
- Breast cancer therapies, like tamoxifen and aromatase inhibitors (AIs), have varying cardiovascular implications.
Purpose of the Study:
- To evaluate the cardiovascular risk factors associated with breast cancer therapies, specifically tamoxifen and aromatase inhibitors (AIs).
- To compare the cardiovascular safety profiles of tamoxifen and AIs.
- To provide guidance for managing cardiovascular risk in breast cancer patients undergoing treatment.
Main Methods:
- Review of current data and clinical trial findings on tamoxifen and AIs.
- Comparative analysis of cardiovascular events, including hypercholesterolemia and thromboembolic events.
- Examination of data from large trials and specific studies like MA.17 comparing AIs to placebo.
Main Results:
- Tamoxifen may lower serum lipids and reduce myocardial infarction risk but increases thromboembolic event risk.
- Aromatase inhibitors (AIs) are not associated with increased thromboembolic or cerebrovascular events.
- Higher hypercholesterolemia incidence with AIs versus tamoxifen may be due to tamoxifen's lipid-lowering effects and trial data differences.
Conclusions:
- Oncologists should consider lifestyle modifications for breast cancer patients to mitigate cardiovascular disease risk.
- Physicians must assess, monitor, and treat cardiovascular risk in breast cancer patients according to established guidelines.
- Aromatase inhibitors appear to have a favorable cardiovascular safety profile compared to tamoxifen regarding specific adverse events.
Abstract:
Cardiovascular disease is the most frequent cause of death in North American women, and so death resulting from cardiovascular disease, rather than from malignancy, is not uncommon in breast cancer patients. This may be a consequence of the shared risk factors for developing breast cancer and cardiovascular disease, as well as the difficulty of managing cancer patients at higher risk for developing cardiovascular disease. Recently, much attention has focused on understanding the cardiovascular risk factors associated with breast cancer therapies. Tamoxifen has a lowering effect on serum lipids and is reported to decrease the risk of myocardial infarction but to increase the risk of thromboembolic events. Current data indicate that aromatase inhibitors (AIs) are not associated with an increased risk of thromboembolic or cerebrovascular events. Reports of a greater incidence of hypercholesterolaemia when AIs are compared head-to-head with tamoxifen may be a result of the intrinsic lipid-lowering effects of tamoxifen therapy and may be confounded by differences in data collection among trials. The incidence of cardiovascular events associated with AIs in large trials has been reported to be higher in trials comparing AIs with tamoxifen; comparisons within the MA.17 trial, which evaluated an AI versus placebo, did not show increases in hypercholesterolaemia or in cardiovascular events with the AI. When treating breast cancer patients, oncologists should consider the same positive lifestyle changes that are proposed to lower the risk of cardiovascular disease in patients who do not have breast cancer. Moreover, physicians should assess cardiovascular risk, and monitor and treat patients already diagnosed with or at risk for coronary heart disease, according to established guidelines.
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