Numerous progestogens are available in Europe for hormone replacement
therapy. Provided that an appropriate dose is given for at least 10 da
ys each cycle, the addition of any of them eliminates the excess risk
of endometrial cancer due to unopposed estrogen therapy. However, andr
ogenic progestogens induce unfavorable metabolic alterations and may r
educe the cardiovascular benefits of estrogen therapy. Although there
is a lack of epidemiological data on the influence on vascular risk of
adding an androgenic progestogen to estrogens, it appears preferable
to use nonandrogenic progestogens. Of these, micronized progesterone,
dydrogesterone, pregnane and norpregnane derivatives constitute the be
st choice for any nonhysterectomized women.