A
recent study published in The Journal of the American Medical Association on
the use or rather the discontinued use of hormone replacement therapy, (HRT)
reveled some interesting results.
The
study’s researcher Gerardo Heiss, MD, professor of epidemiology in the School
of Public Health at the University of North Carolina, Chapel Hill. On the
plus side, some risks associated with the use of the combined estrogen and
progestin therapy disappear after stopping, including increased risks of heart
disease (a leading killer among women) and stroke and blood clots in the lungs.
Unfortunately
the protective effects the hormones provide for hip fracture & colorectal
cancer also disappear. Even two & ½ years later former users have an
increased risk of breast cancer.
The
WHI study was halted in 2002 after an average of 5.6 years of treatment, when
researchers found an increased breast cancer risk among those who took the
hormone therapy vs. those who took a placebo. However the risk of breast cancer
stayed elevated during a follow up the team conducted from July 02 to March 05.
It found “women on HRT had a 27% increased risk” of breast cancer compared to
non-users. They do state that while 79 former HRT users developed breast cancer
during the follow up, 60 nonusers did. However the differences are not
statistically significant.
“When
looking at the breast cancer risk it may have been to soon for the risk to
decline, we do see a tendency toward the breast cancer risk going down”.
This
information was taken from an article written by Kathleen Doheny published on
Oprah.com(http://www.oprah.com/article/health/womenshealth/20090115_orig_HRT_health_risks).
Referenced in this article is researcher Gerardo Heiss, MD, professor of
epidemiology in the School of Public Health at the University of North
Carolina, Chapel Hill, Dr. Rowan T. Chlebowski, MD, PhD, a medical oncologist
at the Los Angeles Biomedical Research Institute in California (also a
researcher on the study).
Keeping
with the hormone replacement topic, many experts find disturbing effects of the
use of conjugated equine estrogens (CEE) used in hormone replacement therapy.
The "estrogen" replacement most doctors prescribe today for
menopausal and premenopausal women is a pill known generically as conjugated
equine estrogens (CEE). The best known brand of CEE is Premarin®. Many studies
suggest that in many women, Premarin does help reduce symptoms of menopause,
including hot flashes, vaginal thinning, memory loss, and urinary incontinence.
It also appears to reduce the risk of developing postmenopausal cardiovascular
disease and osteoporosis.
It also may help to prevent a significant proportion of Alzheimer's disease and
senile dementia.
So
what's wrong with CEE? Premarin is horse estrogen! It is derived from the urine
of pregnant mares, hence, its brand name. Premarin works great in female horses
however replacing human estrogens with horse estrogens may be asking for
trouble.
For the last several million years, the human female reproductive system has
been running quite well on three separate estrogens: estriol, estrone, and
estradiol. Premarin in addition to having larger proportions of estrone and
estradiol, it also contains equilin and two other forms of estrogen found
exclusively in horses.
Premarin is assoiated with a significant risk of breast and endometrial cancer,
because one of the primary effects of equilin, estradiol and estrone is to
promote the growth of tissue in the endometrial (uterine) lining and also in
the breast.
Most conventional physicians, not to mention the self-serving pharmaceutical
industry, are quick to rationalize the cancer and other risks of horse
estrogens. Every treatment has its risks, they point out, but the risk of a
postmenopausal woman dying of a heart attack or stroke if she doesn't take
Premarin are far greater than her risk of dying from cancer or an
osteoporosis-related fracture if she does.
So
what do anti Premarin folks suggest? Triple-Estrogen a combination of natural
estriol, estrone, and estradiol — using molecules identical in structure to
those produced in the human body — in as close-to-natural quantities and
proportions as could be calculated. Triple-Estrogen was formulated by Ed Thorp
of Kripps Pharmacy. In the 16 years since triple estrogen was first prescribed,
thousands of other progressive physicians — and their grateful patients — have
found that it works as well as or better than conventional ERT regimens, while
producing far fewer unwanted side effects.
There
is important evidence dating back to the 1960s suggesting that estriol may
protect against breast cancer as well.
In
the meantime, there can be little doubt that an estrogen replacement regimen
that includes the three human estrogens in Triple estrogen — estriol, estrone,
and estradiol — in identical-to-natural proportions is a superior choice for
perimenopausal and postmenopausal women, compared with the horse estrogens and
100%-estradiol patches and creams the pharmaceutical industry promotes.
Natural hormone formulations like triple estrogen are normally available in the
US
only from compounding pharmacies with a physician's prescription, they can not
be found at standard pharmacies. Natural Progesterone can be purchased in many
health food stores or by mail order.
This
information was published on a website and written by Jonathan V. Wright, MD
and John Morgenthaler (http://www.smart-publications.com/menopause/horse_urine_estrogen_replacement.php)
References: Schliesman B, Robinson L. Serum estrogens: quantitative analysis
of the concentration of estriol compared to estradiol and estrone. MeridianValley
Laboratory. 1997; Kent, WA:Data on file. Premarin® (conjugated estrogen tablets). Wyeth-Ayerst
Company. Physicians' Desk Reference, 52nd Edition. Montvale, NJ:
Medical Economics Company; 1998:3111-3113. Barnes R, Lobo R.
Pharmacology of Estrogens. In: Mishell D, Jr, ed. Menopause: Physiology and
Pharmacology. Chicago:
Year Book Medical Publishers, Inc.; 1987.
Elyce's Story
We’re a small family, a tight knit bunch, and none of us knew exactly how our lives would change when I was diagnosed, but it’s safe to say that not much has been the same ever since...