2. S80 M. Ne6es-e-Castro / Maturitas 43 (2002) S79–S84
gens in the menopause, for hot flashes, sweating, 2. Today’s problems
irritability and libido is certainly the one of Geist
and Spillman [1] in 1932. Before going any further, I think that it is
An enormous contribution to the hormonal relevant to ask some other questions, not about
treatments for menopausal women was done by the good or the bad effects of the treatments with
two pharmaceutical companies: Schering, in Ger- the so called female hormones but, instead, about
many, and Organon, in the Netherlands. The first the objectives that must guide medical practice
pure estrogenic medicines available in the market and the characteristics of the subjects to whom it
were ‘Progynon’ from Schering, ‘Ovestin’ from is addressed.
Organon, ‘Premarin’ from Wyeth. Meanwhile, As physicians, our main goal is to do our best
to preserve and improve health, to prevent dis-
other than pure injectable progesterone, synthetic
eases and to diagnose and treat them well. There-
progestagens were developed and marketed by
fore, there are at least three major concepts:
Schering (‘Primolut’) and Parke Davies (‘Nor-
health maintenance, disease prevention, diagnosis
lutin’). This was what was needed to open a new and treatment of diseases.
era in therapy, specially after Fuller Albright de- The WHO defines Health as ‘a condition of
scribed in 1940 the menopausal osteoporosis due physical, mental and social wellbeing and not only
to hypoestrogenism, and Robert Wilson launched the absence of disease’. Thus; the first step is to
in 1966 a campaign claiming that women could be assess Health, a very complex task much more
‘feminine for ever’ if they were medicated with difficult than the diagnosis of disease.
estrogens. The subject of our attention is a menopausal
However, the first relevant scientific contribu- mid-aged woman. As a menopausal woman, she is
tions to this field were made by three pioneers: hypoestrogenic, and may suffer, at various levels,
Robert B. Greenblatt (USA), Wulf H. Utian from its consequences. But, as a mid-aged
(South Africa, and later in the USA) and Pieter woman, she will suffer, too, from the process of
van Keep (The Netherlands). The first one devel- natural ageing, both from a biological and psy-
oped an enormous experience in the treatment chologic prespective. This is our task to conjugate
with estradiol and testosterone subcutaneous im- and equate the problems, to transform complex
plants; the second, started the first menopause equations into simpler questions, and to find the
clinics and the third founded the International answers that best fit them.
Menopause Society and organized the first Con- What do we know today about postmenopausal
gresses on the Menopause. women?
This was the beginning of many studies in the What do we know about their health promo-
field of the menopause. There was great enthusi- tion strategies, disease prevention and treatments
asm but still little knowledge about doses, combi- with or without female steroid hormones?
There is no doubt that the lifetime risk of
nation treatments, diagnosis of risk factors, etc.
death, for a 50-year-old postmenopausal woman,
Quality of life was no doubt improved and, thus,
is 30% for heart disease, 3% for breast cancer and
women did not want to stop hormonal medica-
3% for hip fracture complications [2].The mortal-
tions. Therefore, treatments were continued non
ity due to heart disease is also much higher than
stop, sometimes with even higher doses and not the mortality due to breast cancer. However, the
associated with progestagens. And, as time went mortality among women who use postmenopausal
on; the first side effects started being reported, as hormones is lower than among nonusers [3].
it was to be expected. Could estrogens cause Therefore, the primary and secondary prevention
endometrial and breast cancer? Could they cause of heart diseases is extremely important. The pre-
vascular diseases? These were some of the ques- vention of osteoporosis comes next. And it goes
tions that the past has sent for the present to without saying that anything that contributes to a
answer. This is where we are now, in the present. better quality of life is equally important.
3. M. Ne6es-e-Castro / Maturitas 43 (2002) S79–S84 S81
Can this be achieved with or without hormonal population that comes to a physician’s office.
treatments, or with a combination of both? For Observational studies are more in line with what
how long? And how does one know if such inter- is done in clinical practice, since the structure of
ventions are indeed being efficacious? What is the the hormones taken is not identical and the doses
result of a benefit/risk analysis, taking into con- administered have been adapted to each individ-
sideration breast cancer and cardiovascular ual; however, they may suffer from possible bias
events? These are the problems of the present time that may interfere with the validity of their con-
that must be solved for the future. clusions. A major misinterpretation of these stud-
I shall not refer to HRT or ERT (replacement ies is the confusion of what is meant by an
therapies) because, after the menopause one is not increased risk. An increased risk e.g. of 50% over
replacing any hormones. One can replace estro- a control group of women does not mean that in
gens in a surgical or premature menopause, or in the treated group half of the women will suffer
cases of gonadal agenesis, but not in the natural that side effect! This is a relative risk; not an
postmenopause when hypoestrogenism is physio- absolute risk! It only means that there will be 50%
logic. One replaces e.g. insulin in a type 1 dia- more cases in the treated group than what was
betic, or cortisone in Addison’s disease. In the already expected in the control group. In the
natural postmenopause one may use hormonal largest observational study [4] on HRT and breast
treatments, just as nonhormonal medicines, but cancer a 35– 50% increased risk after 10–15 years
not hormonal replacements! This is not a question of HRT signifies that it caused only 6– 12 addi-
of semantics. It is, specially nowadays, a funda- tional cases in 1000 women! Furthermore, a study
mental concept to emphasize that hormonal treat- done with a particular progestagen or estrogen,
ments are not necessarily obligatory in the and only with a fixed dose, cannot be extrapo-
postmenopause. They are excellent, if not con- lated to other molecules and regimens. As to the
traindicated, either in the short or long term. And progestagens they can be either pregnane or es-
it is important that women understand and be trane derivatives, without or with androgenic
reassured that there are many different and properties, etc. The pharmacokinetics and efficacy
equally good ways to promote health and prevent of different estrogens are not equivalent. Different
diseases. The importance of a good nutrition, estrogens may have different activities in different
proper exercise and mental occupation are never tissues; the potency and efficacy of a specific
sufficiently stressed by physicians and yet their estrogen can vary from tissue to tissue; and there
consequences may far outweigh the role played by are differences among women with respect to
any remedy. The negative impact of smoking, of estrogens in various tissues [5]. Estrogen receptor
obesity or leanness, in terms of heart and bone b inhibits estrogen receptor a in cells with both
health, are seldom discussed with those women receptors; the cellular sensitivity to estradiol is
who seek hormonal treatments. reduced in cells with both receptors [6]. So, how is
Many clinical trials (prospective) and observa- it possible to extrapolate data from one estrogen
tional studies (retrospective) related to the im- into another one, from one progestagen to
properly so called HRT’s have been recently another?
published, sometimes first in the lay than in the As to the breast cancer increased incidence
medical press. Their interpretation by less critical under hormonal treatments, a major concern
physicians and by the women themselves is open among women and physicians, it is estimated that
to serious mistakes. Most of the fixed protocols only 1 in 397 women taking estrogens over 10
which are required in clinical trials do not neces- years would develop a breast cancer that would
sarily reflect good clinical practice, an art of ad- not ordinarily occurred if estrogen treatments
justing the right dose for a particular woman in were not used [7].
order to avoid side-effects and yet achieve the And 1 excess breast cancer case is likely to
treatment objectives. The selection of women for occur per 5–6 of first myocardial infarction or hip
a clinical trial does not often reflect the general fracture that are prevented [8]. In a recent posthu-
4. S82 M. Ne6es-e-Castro / Maturitas 43 (2002) S79–S84
mous article [9] Trudy Bush wrote that ‘the evi- routes of delivery, doses, or different progestins
dence did not support the hypothesis that estro- have a more favourable or adverse effect on clini-
gen use increases the risk of breast cancer and cal CVD end points’… In a recent publication [15]
that combined hormone therapy increases the risk I wrote that ‘recommendations such as these of
more than estrogen only. Additional observa- the AHA, written as they are, may be less helpful
tional studies are unlikely to alter this conclusion’. than intended, both for clinicians and women’.
A recent reanalysis of individual data from 52 Several well done studies, recently published [16],
epidemiological studies [10] concluded that 1/9 concluded that in postmenopausal women with
women who develop breast cancer may have an stable angina, under treatment with estradiol/
affected mother, sister or daughter, a risk factor norethisterone acetate the number of ischemic
to be kept in mind before the initiation of a events/24 h decreased by 0.82 events after treat-
long-term hormonal treatment in the post- ment compared with an increase in the placebo
menopause. And last, but not least, women who group, of 0.94, a highly significant difference (P=
had breast cancer (clinically cured) and initiated 0.006)! And in the Nurse’s Health Study [17] there
an estrogen treatment had less recurrences and a is evidence that estrogens prevent cardiovascular
longer survival than untreated controls [11]. diseases!
The potential cardiovascular risks increased by These are examples of the difficulties in the
estrogen/progestagen therapies have also been interpretation of many studies that show how
very much emphasized after the conclusions of the limited are the possibilities to extrapolate them
HERS trial. I do not think that these risks are into clinical practice.
realistic in our practice, as I have previously dis- An important recommendation is not to read
cussed [12]. The HERS trial authors are the first only the titles of those publications, or only the
to recognize [13] that ‘the discrepancy between the abstracts. The full paper should be critically read
findings of HERS and the observational studies before one makes up his own mind. Confusions
may also reflect important differences between the are often made between ‘morbidity’ and ‘mortal-
study populations and treatments’ and also that ity’, which are obviously very different. Many
‘for women who stopped taking HERS medica- times those studies refer to ‘woman/year’, a con-
tion, the risk of primary CHD events was elevated cept subject to criticism. When one refers e.g. to
in the 1st month after stopping use of the medica- 100 woman/years this could mean either 100
tion’. And again, they continue with these warn- women treated during 12 months or 400 women
ings: ‘Perhaps postmenopausal hormone therapy treated during 3 months. Would the strength of a
is beneficial in women who have not yet devel- conclusion be the same in either case?
oped coronary disease but not in women who The benefits of estrogen treatments are quite
already have it’ and that ‘the findings of HERS evident for anyone who has a long experience in
should not discourage the use of hormone re- supporting postmenopausal women. We may or
placement therapy in the primary prevention of may not have a good tool for the primary preven-
cardiovascular diseases’. Later on, the American tion of cardiovascular diseases with a very small
Heart Association issued a statement for Health- risk for breast cancer. We may increase bone
care Professionals about HRT and Cardiovascu- mineral density, wether or not fractures are ‘ipso
lar disease [14] where it is written that ‘there are facto’ preventable. We may prevent colon cancer
insufficient data to suggest that HRT should be [18]. We may or may not prevent senile demen-
initiated for the sole purpose of primary preven- tias. But what is quickly visible and felt, by the
tion on CVD’. Most surprisingly, in a foot note of women themselves and by their attending physi-
the same statement, the authors seem to contra- cians, is a remarkable improvement in mood and
dict themselves: ‘the majority of data available to quality of life, by whatever mechanism, with or
make clinical recommendations are based on stan- without the support of measurements of mental
dard doses of oral CEE/MPA. Evidence is insuffi- performance, with appropriate scales. This is
cient to determine whether different preparations, more than enough to contemplate estrogen treat-
5. M. Ne6es-e-Castro / Maturitas 43 (2002) S79–S84 S83
ments, after a proper evaluation of contraindica- estrogens. Nitroglycerin seems to be as efficacious
tions, for the length of time that is needed and as standard estrogen therapy in prevention of
acceptable on the basis of frequent reassessments. oophorectomy-induced bone loss, in women [23],
Let it be remembered that at the central nervous in addition to its vascular effects. Phytoestrogens
system estrogens act like neurotransmitters and may eventually be useful. Testosterone is again
are, so far, the only existing molecules with nerve being considered for some women. Dehidroepi-
growth activity. androsterone is still inconclusive.
Of course there are cases when the so called But the important issue, after all, is not the
HRT is not possible [19] either because it is hormonal treatment after the menopause. What is
contraindicated, or is not wanted by women, or important is the best possible approach to preven-
even because it may not be needed. Under these tive medicine in a mid-aged woman. This requires
circumstances one must carefully evaluate risk from the attending physician (gynaecologist, en-
factors or existing diseases (cardiovascular, can- docrinologist) the development of many talents as
cer, bone, CNS). an empathic human being, capable of establishing
There are nowadays many good nonhormonal a good raport, as an internist, who is able to
medicines that can be used alone or in combina- interprete symptoms that are not necessarily re-
tion(or even in addition to hormonal treatments) lated to his speciality and, no doubt, as a good
like statins, bisphosphonates, thiazide diuretics, well informed scientifically minded specialist.
b-blockers, calcium-chanel blockers, ACE in- This is why I do not think there is a
hibitors, tranquilizers, psychotropics, Vitamin D menopausal medicine; there is only the Medicine
derivatives, calcium, calcitonin, aspirin, etc. And I of mid-aged women who reach the menopause. In
recall what I said before about the unquestionable his lectures Leon Speroff concludes that ‘There is
merits of regular exercise, well balanced nutrition, only one Medicine’. I go one step beyond and say
stop smoking, mental occupation, etc. All the that there are only two Medicines: the Good
above have well proven beneficial effects both for Medicine and the Bad Medicine. Was it not the
symptom relief and for the primary and secondary case, then a gynaecologist would be only confined
prevention of the disease that are more prevalent to the prescription of hormones or would have to
after the menopause [20,21]. be constantly referring the postmenopausal
And worth considering, too, are some other woman to many other different specialists. This
modified estrogen receptor ligands, like SERM’s, referral will only be needed when he becomes
tibolone, or new estradiol conjugates (sulfamates), aware that he has reached the natural limit of his
and newer and better progestagens that are also competence in another area.
being developed (drosperinone). The therapeutic support during the climac-
terium is not confined only to drugs. It is not the
menopause that is going to be treated. It is a
3. The coming days woman, in a very special period of her life, with
affective and hormonal imbalances, who needs to
The future looks promising. The combination be supported and treated as a whole, that she is.
of hormonal and nonhormonal remedies is cer- It is essential to adopt a holistic vision of the
tainly a good strategy to augment the positive middle aged woman and be concerned with all the
effects and to decrease side effects. Lower doses of aspects that define Health (WHO).
hormones are being shown to be as effective as For a woman, the menopause is like an Alarm-
the present standard doses of estrogens. New Clock! An alarm given by Nature, as a reminder
delivery systems are expected to improve treat- that she must stop and reflect about the next 30
ment continuation (compliance). Progestagen years she may still live. An opportunity for a
loaded intrauterine devices [22] can be inserted to check-up. The time to set new goals and define
protect the endometrium and avoid systemic ad- strategies to fulfil them.
ministration of progestagens in association with Sir William Osler once said that ‘Science is an
6. S84 M. Ne6es-e-Castro / Maturitas 43 (2002) S79–S84
art of probability, and Medicine is an art of [10] Beral V. The collaborative Group on Hormonal Factors
uncertainty’. This is the challenge in our daily in Breast Cancer (Oxford). Familial Breast Cancer.
Lancet 2001;358(9291):1389 – 99.
practice. This is why physicians should only give [11] Wren BG. Hormonal therapy following breast cancer. In:
advice, whereas women are the ones who must Neves-e-Castro M, Wren BG, editors. Menopause Hor-
make the decisions. mones and Cancer. London, New York and Washington
Let us not be totally dominated by the Evi- DC: Parthenon Publishing, 2002:55 – 66.
dence Based Medicine and let us allow some room [12] Neves-e-Castro M. The Queen... is naked!. Maturitas
2001;38(3):235 – 7.
for the Medicine Based Evidence. [13] Hulley S, Grady G, Bush T, et al. Randomized trial of
Preventing a woman from the benefits of a estrogen plus progestin for secondary prevention of coro-
sound postmenopausal hormone therapy, because nary heart disease in postmenopausal women. J Am Med
of the fear of rare side effects, does not seem to be Assoc 1998;280:605 – 13.
satisfactory Medicine… Good clinical judgement [14] Mosca L, Collins P, Herrington DM, et al. Hormone
replacement therapy and cardiovascular disease. Circula-
must prevail! tion 2001;104(4):499 –503.
[15] Neves-e-Castro M. Imaginary Woman. Maturitas
2001;40:8 –9.
References [16] Sanderson JE, Haines CJ, Yeung L, et al. Anti-ischemic
action of estrogen-progestogen continuous combined hor-
[1] Geist SH, Spillman F. The therapeutic use of amniotin in mone replacement therapy in postmenopausal women
the menopause. Am J Obstet Gynecol 1932;23:697 –707. with established angina pectoris: a randomised, placebo-
[2] Cummings SR, Black DM, Rubin SM. Lifetime risks of controlled, double-blind, parallel-group trial. J Cardio-
hip, Colles, or vertebral fracture and coronary heart vasc Pharmacol 2001;38(3):372 – 83.
disease among white postmenopausal women. Arch In- [17] Grodstein F, Manson JE, Colditz GA, et al. A prospec-
tern Med 1989;149(11):2445 –8. tive, observational study of postmenopausal hormone
[3] Grodstein F, Stampfer MJ, Colditz GA, et al. Post- therapy and primary prevention of cardiovascular disease.
menopausal hormone therapy and mortality. N Engl J Ann Intern Med 2000;133(12):933 – 41.
Med 1997;336(25):1769 –76. [18] Al-Azzawi F, Wahab M. The relationship of sex steroid
[4] Beral V. The Collaborative Group on Hormonal Factors therapy and colon cancer. In: Neves-e-Castro M, Wren
in Breast Cancer (Oxford). Breast cancer and hormone BG, editors. Menopause Hormones and Cancer. London,
replacement therapy: collaborative reanalysis of data New York and Washington DC: Parthenon Publishing,
from 51 epidemiological studies of 52705 women with 2002:107 – 16.
breast cancer and 108411 women without breast cancer. [19] Neves-e-Castro M. When hormone replacement therapy
Lancet 1997;350:1047 –59. is not possible. In: Studd J, editor. The Management of
[5] Ansbacher R. The pharmacokinetics and efficacy of dif- the Menopause; The Millennium Review. New York Lon-
ferent estrogens are not equivalent. Am J Obstet Gynecol don: Parthenon Publishing, 2000, 2000:91 – 102.
2001;184(3):255 – 63. [20] Genazzani AR, Gambacciani M. Cardiovascular disease
[6] Hall JM, McDonnell DP. The estrogen receptor ß-Isofor and hormone replacement therapy. IMS Expert Work-
(Erß) of the human estrogen receptor modulates ER shop. Climacteric 2000;3:233 – 40.
(transcriptional activity and is a key regulator of the [21] Zhao X-Qyuan C., Hatsukami T.S. et al., Effects of
cellular response to estrogens and antiestrogens. En- prolonged intensive lipid-lowering therapy on the charac-
docrinology 1999;140:5566 –78. teristics of carotid atherosclerotic plaques in vivo by
[7] Santen RJ, Pinkerton JA, McCartney C, et al. Clinical MRI:a case-control study. Arterioscler. Thromb. Vasc.
Review 121: Risk of Breast Cancer with Progestins in Biol. 2001;21(10):1623-29,1563-1564.
Combination with Estrogen as Hormone Replacement [22] Raudaskoski T, Tapanainen J, Tomas E, et al. Intrauter-
Therapy. J Clin Endocrinol Metab 2001;86(1):16 –23. ine 10 microg and 20 microg levonorgestrel systems in
[8] Moerman CJ, Van Hout BA, Bonneux L, et al. Post- postmenopausal women receiving oral estrogen replace-
menopausal hormone therapy: less favourable risk benefit ment therapy: clinical, endometrial and metabolic re-
ratios in healthy Dutch Women. J Intl Med sponse. Br J Obstet Gynaecol 2002;109(2):136 – 44.
2000;248(2):143 – 50. [23] Wimalawansa SJ. Nitroglycerin therapy is as efficacious
[9] Bush TL, Whiteman M, Flaws JA. Hormone replacement as standard estrogen replacement therapy (Premarin) in
therapy and breast cancer: a qualitative review. Obstet prevention of oophorectomy-induced bone loss: A human
Gynecol 2001;98(3):498 –508. pilot clinical study. J Bone Miner Res 2000;15(1):2240 – 4.