HRT During and After Menopause: A Total Eclipse of the Heart? Part 1
Posted on 2011-02-28 21:53:06
The ongoing
mixed messages regarding the cardiovascular safety of hormone replacement
therapy (HRT) in the treatment of menopause are despairing for both patients
and doctors alike. It is important to
think about the relationship between women’s hormones, heart disease, and
menopause in broad principles--otherwise, we’d be a candle in the wind to the
next press release or statistic.
Previously I
have expressed why, I believe, menopausal women considering bioidentical HRT
(BHRT) don’t need to worry as much about breast
cancer. Now, I’d like to focus on
whether or not BHRT is indicated in the prevention of heart disease.
Every year over
400,000 women die of cardiovascular heart disease (as compared to about 40,000
women who die annually of breast cancer) making it the leading
cause of death in women. So, the
impact of bioidentical HRT on heart disease, one way or the other, is of utmost
importance. Notice, I write “BHRT” and
not just “HRT.” This is an important
difference.
Now, without
knowing any statistics, what do we know about women and their hormone cycles, menopause,
and risk of heart disease?
1. Premenopausal,
reproductive, women produce varying daily amounts of estradiol and progesterone
which result in a menstrual period approximately every 28 days, unless they are
pregnant or breast-feeding. The term
“hormonal,” although unfortunately many times used in a derogatory way, is a
good way to remember that reproductive women have different hormone levels at
different times of the month. (Click here and press
"play all" to interactively see how these hormone levels change over
a normal menstrual cycle.)
2. Women in
menopause or postmenopause do not produce ANY significant amounts of estradiol
or progesterone anymore, and therefore have an estrogen and progesterone
deficiency. (Click here to view
hormone levels before, during, and after menopause.)
3. Heart
disease is rare in premenopausal women, more common in prematurely menopausal,
much more common in postmenopausal women, and very common in men.
From the
above basic observations, scientists hypothesized that estrogen was the reason why
women in general, and especially women before menopause, are protected from
heart disease in comparison to men. Estrogen
was thought so much to be protective against heart disease, particularly due to
its positive effects on cholesterol, that in 1963 the oral unopposed estrogen Premarin (which is not
bioidentical) was actually tested in men with heart disease. This counterintuitive use of estrogen (a
primarily female hormone) on these men was attempted because men with a history
of heart disease have the highest risk of recurrent cardiac events and so were
therefore thought ideal candidates for a secondary prevention study of estrogen
which could quickly discern its positive or negative outcomes. In 1966, however, a randomized trial using
Premarin in men with heart disease was stopped early due an increased risk of
blood clots and heart attacks. This negative result halted clinical trials on
estrogens and cardiovascular disease for the next 20 years or so, although
women still used Premarin for menopausal symptoms and classic animal
experiments since the 1950’s continued to demonstrate that estrogens prevent
hardening of the arteries (atherosclerosis) and significantly improve
cholesterol.
In 1987, a
pivotal follow-up report of the Lipids Research Clinics Program,
which observed about 2200 postmenopausal women over 8.5 years, showed that
estrogen (primarily Premarin) significantly reduced cardiac events in
women. In 1991, a UCSD review of 24 observational
studies showed around a 50% reduced risk of cardiac events in postmenopausal
women ingesting Premarin. In 1992, a landmark UCSF meta-analysis
of 32 observational studies showed that postmenopausal women taking Premarin (3
studies included a cyclic progestin) had about a 35% reduced risk of fatal
heart disease. In 1998, at a time when Premarin
was the most commonly prescribed drug in the US, a UCSD meta-analysis of 25
observational studies showed an estimated 30% reduced risk of heart disease
in women using Premarin and a 34% reduced risk in 7 observational studies which
used Premarin and cyclic progestin or cyclic progesterone. In 2001, the Nurses’ Health Study, which
followed over 70,000 healthy postmenopausal women between 1976 and 1996, reported
that nurses taking Premarin showed an approximately 40% reduced risk of cardiovascular
disease.
So why the
change of heart? With all of these
observational studies showing a positive cardiovascular effect, why is there so
much ongoing controversy about whether or not HRT is beneficial for heart
disease? Well, observational studies are
limited in that they may be biased by confounding factors, so the necessary
randomized trials were initiated. The
most famous of these randomized trials, the Women’s Health
Initiative (WHI), was stopped prematurely and claimed in 2002 that HRT
increases the risk of heart disease in healthy postmenopausal women. This was the biggest blow HRT has received in
our lifetime and many women and physicians are still living in fear of its
press releases.
Now, when new information contradicts more than 30 years of observational
knowledge and basic science
and animal experiments, it’s a good time to think twice and start asking
questions before jumping to any conclusions.
These questions will be asked in Part 2 of this article. Some clues to the answers of the paradox are: unopposed estrogen (estrogen administered without a progestin or progesterone) was found to increase the risk of uterine cancer, the type of
hormones used in the Women’s Health Initiative matters, the method of hormone
administration used in the WHI matters, and the difference between bioidentical hormone
replacement therapy and conventional HRT matters.
Look for the continuation:
HRT During and After Menopause – A Total Eclipse of the Heart? Part 2
(coming soon)
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Disclaimer: All the information on this website is intended for educational purposes only, and should not be construed as personal medical advice. Dr. Miller encourages you to do your research and make your own health care decisions with the guidance of a qualified physician.
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