Affiliation:
1. Unit of Reproductive Endocrinology, First Department of Obstetrics and Gynaecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece
2. Division of Endocrinology and Diabetes, "Aghia Sophia" Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece
Abstract
Introduction:
Menopause is associated with adverse effects on quality of life of perimenopausal
and post-menopausal women. It also has an impact on the development of cardiovascular
disease (CVD). Hormonal treatments are the most effective medications for menopausal symptoms
relief. Given the fact that hormonal treatments are contraindicated for many women, non-hormonal
treatment, such as Selective Serotonin Reuptake Inhibitors (SSRIs), Serotonin and Norepinephrine Reuptake
Inhibitors (SNRIs), gabapentin, pregabalin, clonidine and phytoestrogens, constitute alternative
treatments. Nevertheless, little is known about their effects on CVD risk.
Methods:
PubMed, EMBASE and Cochrane Library were searched for the effects of non-hormonal
treatment on CVD risk, blood pressure, heart rate, lipids and glucose concentrations, weight gain, cardiovascular
events, stroke, mortality and morbidity.
Results:
Phytoestrogens, pregabalin and gabapentin seem to have no adverse effects on the cardiovascular
system. Phytoestrogens, in particular, seem to reduce CVD risk through many pathways. On the
other hand, SSRIs and SNRIs, although effective in reducing menopausal vasomotor symptoms, should
be cautiously administered to women with known CVD (e.g. with cardiac arrhythmias, atherosclerotic
disease or stroke). As clonidine has been associated with cardiovascular adverse effects, it should be
administered only in cases where blood pressure regulation is mandatory.
Conclusion:
Further research is needed to produce definite conclusions regarding the cardiovascular
safety of non-hormonal medications for menopausal symptoms relief.
Publisher
Bentham Science Publishers Ltd.
Subject
Cardiology and Cardiovascular Medicine,Pharmacology
Cited by
2 articles.
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