RELIEF FROM HOT
FLASHES:
It
is well established that estrogen replacement provides
relief from hot flashes. The questions investigators are
asking now relate to the most effective form of estrogen
replacement. For example, Simon and colleagues recently
compared estrogen-androgen therapy with estrogen-only
therapy for efficacy in relieving vasomotor symptoms. In
their trial, 93 patients were randomized to receive 1 of 5
daily regimens for 3 months: oral CEE (0.625 mg or 1.25 mg),
oral CEE combined with methyltestosterone (0.625 mg and 1.25
mg or 1.25 mg
and 2.5 mg), or placebo. These investigators found that the
extent of relief with the lower-dose estrogen-androgen
treatment was similar to
that achieved with the higher-dose estrogen-only
treatment. The data also suggested that 1.25 mg/day oral CEE
can produce a hypoandrogenic state because of the
induced rise of sex hormone-binding globulin
(SHBG), which reduces the bioavailable testosterone. This
may however
have implications for sexual function.
ESTROGEN METHODS:
Currently,
estrogen replacement is delivered orally or transdermally;
both means have disadvantages, including variable
bioavailability, intestinal and hepatic first-pass effects
(oral), and dermatologic reactions (transdermal). Studd and
coworkers studied the efficacy and acceptability of
intranasal E2 (S21400), which was designed to bypass these
drawbacks. In a 3-month, double-blind study, 420 women
were randomized to receive 1 of 4 daily dosage regimens of
intranasal S21400 (100, 200, 300, or 400 mcg),
intranasal placebo, or oral E2 valerate (1 or 2 mg). The
incidence of hot flushes decreased by 75% with 200 mcg/day
S21400 at 4 weeks. Except for a greater incidence of
sneezing and application-site reaction (99% mild or
moderate), there were no significant effects on ear, nose,
or throat function or adverse events, compared with placebo
and oral E2. Overall, the study found that intranasal E2 was
significantly more effective than placebo and about as
effective as oral E2 in relieving menopausal symptoms and
was well tolerated. Another recent study showed that
intranasal E2 (300 mcg/day) normalized bone turnover to
premenopausal levels within 3 months. Thus, it appears that
we may have a new option for HRT, one that avoids first-pass
metabolism and provides a reproducible and easily adjustable
dosing mechanism.
Of note are
recent findings that women who have no vasomotor symptoms
when they begin HRT do not develop such symptoms when
treatment is first instituted and then abruptly stopped
after 3 months. This may be useful information for a
clinician to provide a patient who is undecided about
whether to begin HRT when she is not experiencing vasomotor
symptoms.
WHAT ESTROGEN IS NOT:
Estrogen is not one hormone, it is the name of a group of
hormones. There are three principle forms of estrogen found
in the human body estrone, estradiol and estriol, also known
as E1, E2 and E3 respectively. There is also a group of
compounds called phytoestrogens, generally found in food,
which can have "estrogen like" effects in the body.
Estradiol (E2) is the primary estrogen produced by the
ovaries. Estrone (E1) is formed from estradiol. It is a weak
estrogen and is the most abundant estrogen found in the body
after menopause. Estriol (E3) is produced in large amounts
during pregnancy and is a breakdown product of estradiol.
Estriol is also a weak estrogen and may have anti-cancer
effects. Before menopause estradiol is the predominant
estrogen. After menopause estradiol levels drop more than
estrone so that now estrone is the predominant estrogen.
For
the past 50 years, conjugated equine estrogen, brand name
Premarin® has been the most commonly prescribed estrogen
supplement in the U.S. Conjugated estrogens are derived from
pregnant mare's urine. They must be converted by the body
into active estrogens. Premarin® is the most studied
estrogen supplement. It is also the most widely prescribed
hormone in the world. If you are taking a hormone, it is
probably Premarin®. Estradiol (E2) is now widely prescribed
in the form of skin patches, tablets and creams and is
gaining on premarin in popularity. A combination of E1,E2
and E3 called Triple Estrogen or Tri-Est,has been available
for many years. It's proponents claim it is the most natural
way to take estrogen. Triple estrogen is difficult to get.
It is generally available only by mail order
THE MOST EFFECTIVE HERB:
One
of the most effective herbal products available today,
Imperial Gold Maca™ has been making a strong presence in the
United States and many foreign countries. Sold usually
in health food stores or by women who have used the product
and now distribute it, Imperial Gold Maca™ seems to be
coming the natural choice of most women. With a reputation
of no known side effects, which is highly
desirable, Imperial Gold Maca™ may
increase energy, stamina, alertness and fertility
enhancement. User's who have tried drug products rave of the
natural benefits. Gaining popularity slowly, it seems to be
a word of mouth campaign conducted by the 1000's of women
who are currently advocates of this herb that may seems to
promote estrogen and progesterone naturally. The best source
of progesterone and estrogen is your own body. For the most
part, nothing could be more natural, and carry no risk of
known side effects.
MACA
So What Is
Natural ?
So which is
natural? Is natural better? If so why? It all depends on
what YOU consider natural, remember, there are many
"natural" poisons. If you consider "natural", that which
occurs in the body in the highest concentration after
menopause, then estrone is the natural estrogen for you.
Estrone is easy to get. Most of the prescription estrogens
when taken by mouth are converted in your GI tract and end
up predominantly as estrone.
If you consider natural, getting your estrogen levels up to
where they were before menopause then estradiol is
your natural estrogen. The transdermal patches, vaginal
rings and estradiol creams provide pre-menopausal levels of estradiol
.If you desire a natural estrogen that is the least likely
to cause cancer then estriol may be right. Tri-Est contains
mostly estriol. However a dose high enough to prevent hot
flashes causes nausea. There for the pharmacies add 10% E1
and 10% E2 to Tri-Est. So its mostly, but not totally,
estriol.
To some people natural means "not produced in the lab". They
prefer to use herbs, or eat a diet high in phytoestrogens.
ALL of the above estrogens are produced in the lab no
matter what it says on the label.
Phytoestrogens or plant estrogens are very weak estrogens
and must be taken in large quantities to have an desirable
effect. Some foods have high levels of phytoestrogens. These
compounds are found in soy foods, some beans, flax seeds,
and some herbs. The phytoestrogenic compounds are called
isoflavones and lignans.
See
Maca
for natural hormonal balancing.
The Following
Lists the Most
Commonly Used Estrogens
(NOTE:
Imperial Gold Maca™ is Not An Estrogen But A Natural Herbal
Supplement
That Allows The Body To Stimulate Estrogen Naturally On It's
Own)
PLANT
BASED |
Drug Name
or Herb |
Route |
Years |
FDA
Approved or Herbal
Requiring No FDA Approval |
Strength |
Cost/Day* |
Alora® |
Transdermal |
1 |
Menopausal
Syndrome |
0.05 mg
0.075 mg
0.1 mg |
0.72
0.72
0.72
|
Cenestin® |
Oral |
1 |
Menopausal
Syndrome |
0.625 mg
0.9 mg |
0.37
0.37 |
Climara® |
Transdermal |
1 |
Menopausal
Syndrome |
0.05 mg
0.75 mg
0.1 mg |
0.72
0.72
0.72 |
Estrace® |
Oral
Vaginal |
20
10 |
Menopausal
Syndrome
Osteoporosis
Vaginal Atrophy |
0.5 mg
1.0 mg
2.0 mg
0.1% cream |
0.31
0.38
0.56
1.61 |
Estroderm® |
Transdermal |
10 |
Menopausal
Syndrome
Osteoporosis |
0.05 mg
0.1 mg |
0.72
0.80 |
Estratab® |
Oral |
20 |
Menopausal
Syndrome
Osteoporosis |
0.3 mg
0.625 mg
1.25 mg
2.5 mg |
0.32
0.32
0.32
0.32 |
Estring® |
Vaginal Ring |
1 |
Vaginal Atrophy |
5-10 mg |
|
FemPatch® |
Transdermal |
1 |
Menopausal
Syndrome |
0.05 mg
0.1 mg |
0.72
0.72 |
Imperial Gold
Maca™
(Herbal Requiring No FDA
Approval)
|
Oral |
100+ |
Menopausal
Syndrome
Osteoporosis
Vaginal Atrophy
Fatigue
Fertility
Aphrodisiac
Mental Clarity |
550 mg
Suggested 5 Daily For
First Week For Maximum
Results. |
0.20 |
Menest® |
Oral |
20 |
Menopausal
Syndrome |
0.3 mg
0.625 mg
1.25 mg
2.5 mg |
0.32
0.32
0.32
0.32 |
Ogen® |
Oral |
40 |
Menopausal
Syndrome
Osteoporosis |
0.625 mg
1.25 |
0.58
0.77 |
Ortho-est® |
Oral |
2 |
Menopausal
Syndrome |
0.625 mg
1.25 mg |
0.58
0.77 |
Vivelle® |
Transdermal |
1 |
Menopausal
Syndrome |
0.037 mg
0.05
0.75
0.1 |
0.72
0.72
0.72
0.72 |
ANIMAL
BASED |
Drug Name |
Route |
Years |
FDA
Approved for |
Strength |
Cost/Day* |
Premarin® |
Oral |
50 |
Menopausal
Syndrome
Osteoporosis |
0.3 mg
0.625 mg
0.9 mg
1.25 mg
2.5 mg |
0.37
0.37
0.37
0.37
0.37 |
ESTROGEN/PROGESTERONE COMBINATIONS |
Drug Name |
Route |
Years |
FDA
Approved for |
Strength |
Cost/day* |
CombiPatch® |
Transdermal |
1 |
Menopausal
Syndrome |
0.05 mg
estradiol
0.14 mg
norethindrone |
0.72 |
femhrt® |
Oral |
1 |
Menopausal
Syndrome
Osteoporosis |
5 mcg
ethinyl estradiol
1 mg
norethindrone
continous |
0.73 |
Ortho-Prefest® |
Oral |
1 |
Menopausal
Syndrome
Osteoporosis |
1 mg
estradiol
0.09 mg
norgestimate
sequential |
0.73 |
Prempro® |
Oral |
5 |
Menopausal
Syndrome
Osteoporosis |
0.625 mg
premarin
2.5 mg
cycrin
continous |
0.73 |
Premphase® |
Oral |
5 |
Menopausal
Syndrome
Osteoporosis |
0.625 mg
premarin
5 mg
cycrin
sequential |
0.73 |
ESTROGEN -
ANDROGEN COMBINATIONS |
Drug Name |
Route |
Years |
FDA
Approved for |
Strength |
Cost/Day* |
Estratest® |
Oral |
5 |
Menopausal
Syndrome
Osteoporosis |
1.25/2.5 mg |
0.90 |
Estratest HS® |
Oral |
5 |
Menopausal
Syndrome
Osteoporosis |
0.625/1.25 mg |
0.74 |
All costs
shown are approximate. Costs will differ with individual
pharmacies and/or drug plans.
|
Copyright © 2000-2018 ImperialGoldMaca.com. All Rights Reserved.
11814 83rd Avenue Suite 6-F Kew Gardens,New York 11415 USA
Privacy
Statement |
Safe Shopping |
Terms Of Use |
Copyrighted Material
|