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Dr. John Lee and
Dr. Ellen Grant had a longstanding disagreement about natural
progesterone and its effects, but until recently it was a heated
debate between physicians. Now Dr. Grant and Lynne McTaggart
have launched a personal attack against Dr. Lee in the
newsletter What Doctors Don’t Tell You (WDDTY). Dr. Grant’s
article about progesterone and breast cancer, titled “Cancer in
a Cream?” sounds convincing on the surface, but in truth it’s
hopelessly muddled and riddled with inconsistencies and
inaccuracies.
Dr. Lee greatly
admired the early and pioneering work Dr. Grant did exposing the
first birth control pills as dangerous, and he felt she had been
instrumental in galvanizing drug companies to create safer oral
contraceptives, probably saving thousands of lives in the
process. He expressed that admiration, both to her personally
and in his talks and books. The fact that Dr. Grant is now
attacking someone who isn’t here to defend himself speaks
volumes, but there are many of us who are here to defend Dr. Lee
and set the record straight.
WDDTY Editor
Lynne McTaggart introduces Dr. Grant’s article in an editorial
that describes Dr. Lee as “proselytizing” and describes his
point of view as “not only wrong, but dangerous.” The fact is
that the science and research behind Dr. Lee’s work is more
solid than ever, and new research comes out every month that
supports it. Thousands of doctors in clinical practice—which is
where the rubber meets the road—are turning to bioidentical
hormones because they’re safer and work better.
Dr. Ellen
Grant and Lynne McTaggart of WDDTY Make Factual Errors
In contrast, Dr.
Grant’s article doesn’t even provide us with a good scientific
debate, because her reasoning is so muddled and her foundational
assertions aren’t correct. For example, Dr. Grant continues to
base many of her arguments about natural progesterone on
research with synthetic progestins. She admits they’re
different, but argues as if they’re the same. Yes, they have
some common actions in the body, but they also differ
enormously. No reputable scientist or physician disputes the
fact that progesterone and progestins are different, but Dr.
Grant has continued to insist over the years that research on
progestins applies to progesterone. In her WDDTY article, she
repeatedly switches back and forth between statements about
progestins and progesterone, as if they are interchangeable.
Ms. McTaggart
compounds this misunderstanding by claiming that natural
progesterone really isn’t natural because it is “…a substance
made in the laboratory by taking the sterol base of wild yam and
chemically tweaking it, adding molecules here and there until
you produced something with the same molecular blueprint as
ovary-derived progesterone.” Dr. Ellen Grant makes a similar
statement, that progesterone “…approximate[s] the compound [sic]
the female ovary produces.”
As Dr. Lee used
to say, “a rose is a rose is a rose, and progesterone is
progesterone is progesterone.” It’s either progesterone, or it’s
not. It either has the same molecular structure, or it doesn’t.
The progesterone known as “natural” progesterone is the exact
same molecule as so-called ovary-derived or bioidentical
progesterone. This is a fact.
Research on
Progesterone and Breast Cancer
After the factual
errors, which cast a shadow over all of Lynne McTaggart and Dr.
Grant’s assertions, is the premise that one can declare
“progesterone causes breast cancer” based on in vitro (test
tube) research with a couple of breast cancer cell lines. As Dr.
Lee repeatedly pointed out, test tube research is
one-dimensional, while progesterone’s actions in the human body
are affected and mediated by dozens of other factors, including
organs, glands, hormones, the immune system, lifestyle and
genes—to name a few. Test tube research can only suggest a
possible theory for further exploration.
Breast cancer
researcher Dr. David Zava, our co-author of What Your Doctor May
Not Tell You about Breast Cancer,” and a great friend and
colleague of Dr. Lee, spent thousands of hours studying these
same breast cancer lines. He explains, “It’s ludicrous to
extrapolate this research to humans without an in-depth
understanding of biochemistry and physiology. The reality of how
progesterone affects breast tissue is far more
complex—progesterone is only one piece of the puzzle. The
research Dr. Grant cites is good, solid scientific work, and
very interesting, but it is not even close to enough information
to declare that progesterone is carcinogenic. In fact, there’s
far more research showing the opposite—that progesterone is
protective against breast cancer—and in addition to that there’s
clinical data, done with real women that shows it’s protective.”
As for test tube
studies, there are dozens, if not hundreds, showing that
progesterone reduces cell proliferation, encourages apoptosis
(cell death), and stimulates differentiation of cells—all
important factors in preventing breast cancer. There’s a buzz
out there right now in the research community about the p53
gene’s possibilities in preventing and treating breast cancer
and guess what? Progesterone upregulates the p53 gene, a nice
little piece of test tube research done about a decade ago that
pointed the way to much other research on progesterone and p53.
Real
Progesterone Research with Real Women
Let’s briefly
review some of the clinical data—meaning research with real,
live human women—on progesterone and breast cancer. If you’d
like details and more research, please read What Your Doctor May
Not Tell You about Breast Cancer.
1) The earliest
clinical study that we know of on progesterone and breast cancer
was done at Johns Hopkins University back in 1981 (Cowan et al,
American Journal of Epidemiology). They measured estrogen and
progesterone in a group of women, then divided them into two
groups: those with normal progesterone levels and those with low
progesterone levels. They followed these women for 20 years and
found that in the women with low progesterone, the incidence of
breast cancer was over 80 percent greater than those with normal
progesterone, and the incidence of all cancers was ten times
higher than in women with normal progesterone.
2) In 1996,
researchers measured women’s progesterone before breast cancer
surgery and found that those with normal progesterone levels had
an 18-year survival rate—twice that of women with low
progesterone at the time of surgery. (Mohr et al, British
Journal of Cancer)
3) Three studies
in particular have shown progesterone’s effect on breast cells.
One, by Foidart et al and published in the journal Fertility and
Sterility in 1998 concluded, “Exposure to progesterone for 14
days reduced the estradiol-induced proliferation of normal
breast epithelial cells in vivo.” Another, by Malet et al and
published in the Journal of Steroid Biochemistry and Molecular
Biology, in 2000 concluded, “Cells exhibited a proliferative
appearance after E2 [estradiol] treatment, and returned to a
quiescent appearance when P[rogesterone] was added to E2.
P[rogesterone] appear(s) predominantly to inhibit cell growth,
both in the presence and absence of E2.”
The third study
tested the effects of transdermal (rubbed into the skin)
hormones in healthy young women planning to undergo minor breast
surgery for aesthetic reasons or for benign breast disease. Ten
to 13 days before surgery, four groups of women applied either
estradiol cream, progesterone cream, a combination of estradiol
and progesterone or a placebo cream (with no hormones in it). At
surgery, biopsies were done to measure estrogen and progesterone
levels, and the level of cell proliferation rates. (High levels
of cell proliferation is a marker for breast cancer.) The study
demonstrated that both hormones were well absorbed through the
skin into the breast tissue. But even more significant,
estradiol increased cell proliferation by 230 percent, whereas
progesterone decreased it by more than 400 percent. The
estradiol-progesterone combination maintained the normal
proliferation rate. (Chang et al, Fertility and Sterility)
4) In 2002, a
French study of HRT in 3,175 women was released. This was
particularly interesting because it was a large study, and
because, to quote the study, “...the main specificity of the
French cohort is that 83% of the combined HRT users were
receiving mostly or exclusively a transdermal estradiol gel
formulation, and the progestin was oral micronized progesterone
in 58%, while MPA users were less than 3%.” Oral micronized
progesterone is bioidentical, natural progesterone, which is
what most French women use, rather than the synthetic progestins.
The conclusion of the study was that, “When both duration of use
and the last period of use were analyzed together, no
significant increase in breast cancer incidence was observed in
any of the four subgroups considered,” and “From internal
analysis, there was no significant increase in the risk of
breast cancer related to use of the specific type of HRT most
prescribed in France.”
Moderation and
Common Sense are the Keys to Optimal Health
One of the
aspects of Dr. Lee’s character that I admired most was his
willingness to change course and moderate his message when new
evidence was brought to his attention. He was first led to
progesterone when he realized that the conventional HRT he had
been prescribing for years had probably harmed many women. He
had the courage to admit this first to himself, then to his
patients, and he then set about solving the puzzle of how to
help women balance their hormones safely and effectively. The
discovery of progesterone as a neglected piece of the hormone
balance puzzle was exciting and yes, he was a man on a mission
to help women balance their hormones and to help undo the damage
of conventional HRT. As a result of his courage and zeal,
millions of women are healthier and happier.
From the
beginning, Dr. Lee recommended no more than 15 to 30 mg of
progesterone daily for the majority of women, and for
premenopausal women for just two weeks per cycle. This is a very
moderate dose that approximates what the ovary would be making
in a normal premenopausal woman. Furthermore, he advocated
splitting the dose and taking half in the a.m. and half in the
p.m.
There’s no doubt
that it’s not a good idea for most women to take large doses of
progesterone in any form over a long period of time. That’s just
not good medicine, it’s not balanced, it’s not common sense, and
it’s bound to cause trouble sooner or later. In his first
self-published book for doctors, Dr. Lee likened the “dance of
the steroids” to an orchestra, where each player creates
beautiful music by being in harmony and rhythm with the others.
Large doses of progesterone will drown out the other players and
create chaos.
As zealous as Dr.
Lee was about progesterone, his message was never just about one
hormone. He always strongly advocated a wholesome diet, moderate
exercise, good sleep, stress management, healthy relationships
with others, and the importance of making time for fun and for
contemplation.
The quest for
optimal health is never-ending, and ever-changing, and is best
addressed on all levels: physical, emotional, mental and
spiritual. There’s no magic potion or lotion. Optimal health is
an ongoing, evolving journey of discovery.
Please Pass
This On
The Dr. Ellen
Grant – Lynne McTaggart article has created quite a stir because
it was widely spread around on the internet, and as I said
earlier, it sounds quite convincing if you’re not familiar with
the research. However, the information on breast cancer, as well
as the additional information about progesterone and the immune
system, isn’t accurate or convincing once you have the facts in
hand.
There’s a lot of
misinformation about progesterone being spread around right now.
It’s probably not coincidental that this well-financed and
well-orchestrated campaign coincides with Wyeth-Ayerst’s
petition to the FDA demanding that compounding pharmacists not
be allowed to dispense natural hormones. (Wyeth-Ayerst is the
maker of PremPro.) If they succeed in pressuring the FDA into
making progesterone made a prescription-only, brand name drug,
it will be interesting to watch how quickly they come out with a
progesterone cream, patch or pill themselves.
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