Hormone replacement therapy (HRT) was initially given to protect women agai
nst osteoporosis and alleviate menopausal symptoms, such as hot hashes, dep
ression, sleep disturbances, and vaginal dryness. In view of the understand
ing of oestrogen deficiency as a major trigger for the acceleration of card
iovascular risk after menopause, HRT may also be proposed as a substantial
beneficial cardioprotective agent. Progestins, which may be added to oestro
gen in combined HRT to reduce the risk of uterine malignancy, have a number
of potential adverse effects on the cardiovascular system which could even
attenuate the benefit of unopposed oestrogen replacement therapy in post-m
enopausal women.