Menopause
Resource Center
Facts
About Postmenopausal
Hormone Therapy
article syndicated from NHLBI
NOTE:
Since this fact sheet was written in October 2002,
a development has occurred that may affect your health
decisions. The National Institutes of Health stopped
the estrogen-alone study of the Women's Health Initiative
(WHI).
Choosing
whether or not
to use postmenopausal
hormone therapy
can be one of the
most important
health decisions
women face as they
age. As with taking
any treatment,
the decision involves
carefully weighing
the risks and benefits
involved.
But,
until recently, the
picture of those
risks and benefits
has been unclear.
Studies gave conflicting
results about the
therapy's effects
on breast cancer,
heart disease, and
other conditions.
Box
1
|
Oral
Estrogen
and Estrogen/Progestin
Products*
|
Estrogen
pills:
|
Premarin
|
conjugated
equine
estrogens
|
Cenestin
|
synthetic
conjugated
estrogens
|
Estratab
|
esterified
estrogens
|
Menest
|
esterified
estrogens
|
Ortho-Est
|
estropipate
(piperazine
estrone
sulfate)
|
Ogen
|
estropipate
(piperazine
estrone
sulfate)
|
Estrace
|
micronized
17-beta-estradiol
|
Progestin
pills:
|
Amen
|
medroxyprogesterone
acetate
|
Cycrin
|
medroxyprogesterone
acetate
|
Provera
|
medroxyprogesterone
acetate
|
Micronor
|
norethindrone
|
Nor-QD
|
norethindrone
|
Aygestin
|
norethindrone
acetate
|
Ovrette
|
norgestrel
|
Norplant
|
levonorgestrel
|
Prometrium
|
progesterone
USP (in
peanut
oil)
|
Megace
|
megestrol
acetate
(not for
uterine
protection)
|
Estrogen
plus
progestin
pills:
|
Premphase
|
conjugated
equine
estrogens
and medroxyprogesterone
acetate
|
Prempro
|
conjugated
equine
estrogens
and medroxyprogesterone
acetate
|
Femhrt
|
ethinylestradiol
and norethindrone
acetate
|
Activella
|
17-beta-estradiol
and norethindrone
ecetate
|
Ortho-Prefest
|
17-beta-estradiol
and norgestimate
|
*
As
of
Fall
2000
|
Back to Top
In
the summer of 2002,
new findings emerged
that have finally
begun to fill in
some of the picture's
details. While
much more remains
to be learned,
the findings offer
women some guidance
about the risks
and benefits of
using postmenopausal
hormone therapy.
This
fact sheet discusses
those findings and
gives you an overview
of such topics as
menopause, hormone
therapy, and alternative
treatments to the
symptoms of menopause
and various health
risks that come in
its wake. It also
provides a list of
sources you can contact
for more information.
If
you're on hormone
therapywhether
short- or long-term
useyou're bound
to have a lot of
concerns. This fact
sheet will provide
some information,
but it's important
to talk with your
doctor or other health
care provider about
your health profile.
Being informed is
one of the best ways
you can protect your
health.
Box 2
|
Gels,
Creams,
Patches,
and
Other
Hormone
Products*
|
Estrogen
products:
|
Cream
|
Estrace
|
micronized
17-beta-estradiol
|
| |
Ortho
Dienestrol
|
dienestrol
|
| |
Premarin
|
conjugated
equine
estrogens
|
Vaginal
Tablet
|
Vagifem
|
estradiol
hemihydrate
|
Vaginal
Ring
|
Estring
|
micronized
17-beta-estradiol
|
Skin
Patch
|
Alora
|
micronized
17-beta-estradiol
|
| |
Climara
|
micronized
17-beta-estradiol
|
| |
Esclim
|
micronized
17-beta-estradiol
|
| |
Estraderm
|
micronized
17-beta-estradiol
|
| |
Vivelle
|
micronized
17-beta-estradiol
|
| |
Vivelle-Dot
|
micronized
17-beta-estradiol
|
Progestin
products:
|
Vaginal
Gel
|
Crinone
|
progesterone
|
Injection
|
Depo-Provera
|
medroxyprogesterone
acetate
(not for
uterine
protection)
|
IUD
|
Mirena
|
levonorgestrel
|
| |
Progestasert
|
progesterone
|
Estrogen
plus
progestin
products:
|
Skin
Patch
|
Combipatch
|
17-beta-estradiol
and norethindrone
acetate
|
Ortho-Prefest
|
17-beta-estradiol
and norgestimate
|
Injection
|
Depo-Testadiol
|
testosterone
and estradiol
cypionate
|
*
As
of
Fall
2000
|
Back to Top
Menopause
and Hormone Therapy
As
you age, significant
internal changes
take place that affect
your production of
the two female hormones,
estrogen and progesterone.
The hormones, which
are important in
regulating the menstrual
cycle and having
a successful pregnancy,
are produced by the
ovaries, two small,
oval-shaped organs.
During
the years just before
menopause, known
as perimenopause,
your ovaries begin
to shrink. Levels
of estrogen and progesterone
fluctuate as your
ovaries try to keep
up production of
the hormones. You
can have irregular
menstrual cycles,
along with unpredictable
episodes of heavy
bleeding during a
period. Perimenopause
usually lasts several
years.
Eventually, your periods stop. Menopause marks the
time of your last
menstrual period.
It is not considered
the last until you
have been period-free
for 1 year without
being ill, pregnant,
breast-feeding, or
using certain medicines,
all of which also
can cause menstrual
cycles to cease.
There should be no
bleeding, even spotting,
during that year.
Natural menopause
usually happens sometime
between the ages
of 45 and 54.
You
also can undergo
menopause as the
result of surgery.
A surgical procedure,
called a hysterectomy,
removes the uterus
and sometimes the
ovaries and fallopian
tubes as well. You
go through menopause
if both of your ovaries
are removed. Otherwise,
the surgery does
not affect menopause,
which still occurs
naturally.
Whether
you go through menopause
naturally or surgically,
symptoms can result
as your body tries
to adjust to the
drop in estrogen
levels. These symptoms
vary greatlyone
woman may breeze
through menopause
with few symptoms,
while another has
difficulty. Symptoms
may last for several
months or years,
or persist. The most
common symptoms are
hot flashes or flushes,
sweats, and sleep
disturbances. (A
hot flash is a feeling
of heat in your face
and upper body, which
may cause the skin
to appear flushed
or red as blood vessels
expand. Hot flashes
that occur with severe
sweating during sleep
are called night
sweats.) But the
drop in estrogen
also can contribute
to other symptoms,
such as changes in
the vaginal and urinary
tracts, which can
cause painful intercourse,
urinary infections,
and the need to urinate
more often.
Box
3
|
Hormone
Therapy
Schedules
- Cyclic
or
sequentialEstrogen
for
25
or
30
days
a month,
with
progestin
added
for
10-14
days
- Continuous-combinedEstrogen
and
progestin
daily
|
To
relieve the symptoms
of menopause, doctors
may prescribe postmenopausal
hormone therapy.
This can involve
the use of either
estrogen alone
or with another
hormone called
progesterone, or
progestin in its
synthetic form.
The two hormones
normally help to
regulate a woman's
menstrual cycle.
Progestin is added
to estrogen to
prevent the overgrowth
(or hyperplasia)
of cells in the
lining of the uterus.
This overgrowth
can lead to uterine
cancer. If you
haven't had a hysterectomy,
you'll receive
estrogen plus progestin
therapy; if you
have had a hysterectomy,
you'll receive
estrogen-only therapy.
Hormones may be
taken daily (continuous
use) or on only
certain days of
the month (cyclic
use).
They
also can be taken
in several ways,
including orally,
through a patch on
the skin, as a cream
or gel, or with an
intrauterine device
(IUD) or vaginal
ring. How the therapy
is taken can depend
on its purpose. For
instance, a vaginal
estrogen ring or
cream can ease vaginal
dryness, urinary
leakage, or vaginal
or urinary infections,
but does not relieve
hot flashes.
Hormone
therapy may cause
side effects, such
as bleeding, bloating,
breast tenderness
or enlargement, headaches,
mood changes, and
nausea. Further,
side effects vary
by how the hormone
is taken. For instance,
a patch may cause
irritation at the
site where it's applied.
Box
1, Box
2, and Box
3 list products
and schedules for
various hormone therapies.
There also are nonhormonal
approaches to easing
the symptoms of menopause. Box
4 offers a list
of some of these
alternatives.
Back to Top
Box
4
|
Alternatives
to Hormone
Therapy
to Help
Prevent
Postmenopausal
Conditions
and Relieve
Menopausal
Symptoms
You
may want
to consider
alternatives
to hormone
therapy
to ease
menopausal
symptoms.
The list
below
includes
some
locally
applied
hormone
products
(which
may not
carry
the same
risks
as those
that
deliver
medication
throughout
the body),
dietary
supplements,
and lifestyle
measures.
Talk
with
your
doctor
or other
health
care
provider
about
the best
treatment
for you
for each
symptom.
Be
aware
that,
unlike
drugs,
the U.S.
Food
and Drug
Administration
(FDA)
does
not have
the authority
to approve
dietary
supplements
before
they
are sold.
The dietary
supplement
manufacturer
is responsible
for insuring
that
the product
is safe
and that
any representations
or claims
made
about
it are
adequately
substantiated
and not
false
or misleading
(see
Box 5).
One
positive
move
you can
make
to feel
better
is to
adopt
a healthy
lifestyledon't
smoke,
eat a
variety
of foods
low in
saturated
fat and
cholesterol
and moderate
in total
fat,
maintain
a healthy
weight,
and be
physically
active.
For
postmenopausal
conditions:
Osteoporosis
- See
Box
20 for
lifestyle
behaviors
to
protect
bone
density
- Designer
estrogen
Raloxifene
(Evista),
which
preserves
bone
density
- Bisphosphonates
Actonel
or
Fosamax,
which
reverse
bone
loss
and
prevent
fractures
- Calcitonin
(a
nasal
spray),
which
may
prevent
fractures
- Note:
Phytoestrogens
(see "Hot
flashes" below)
have
not
been
shown
to
reduce
fractures
Heart
disease
- Lifestyle
behaviors,
including:
- Following
a healthy eating plan
- Limiting
consumption of alcoholic beverages
- Not
smoking
- Maintaining
a healthy weight
- Being
physically active
- Preventing
and
controlling
high
blood
pressure
- Preventing
and
controlling
high
blood
cholesterol
- Managing
diabetes
- Taking
prescribed
medication
to
control
heart
disease
For
menopausal
symptoms:
Hot
flashes
- Lifestyle
changes. These
include
dressing
and
eating
to
avoid
being
too
warm,
sleeping
in
a
cool
room,
and
reducing
stress.
Avoid
spicy
foods
and
caffeine.
Try
deep
breathing
and
stress
reduction
techniques,
including
meditation
and
other
relaxation
methods.
- Soy. This
contains
phytoestrogens.
(Phytoestrogens
are
estrogen-like
substances
derived
from
a plant
source.)
However,
there
is
no
solid
evidence
that
soyor
other
sources
of
phytoestrogensreally
do
relieve
hot
flashes.
Further,
the
risks
of
taking
soy,
especially
the
more
concentrated
forms
of
soy,
such
as
pills
and
powders,
are
not
known.
Phytoestrogens
from
soy
can
be
consumed
through
foods
or
supplements.
Soy
food
products
include
tofu,
tempeh,
soy
milk,
and
soy
nuts.
These
soy
products
are
more
likely
to
work
on
mild
hot
flashes.
- Other
sources
of
phytoestrogens. These
include
such
herbs
as
black
cohosh,
a
member
of
the
buttercup
family,
wild
yam,
dong
quai,
and
valerian
root.
- Antidepressants, such
as
Effexor,
Paxil,
and
Prozac
have
been
proved
moderately
effective
in
clinical
trials;
however,
they
have
not
been
approved
for
this
use.
Vaginal
dryness
- Vaginal
lubricants
and
moisturizers
(available
over
the
counter).
- Products
that
release
estrogen
locally
(such
as
vaginal
creams,
a vaginal
suppository,
called
Vagifem,
and
a plastic
ring,
called
an
Estring)these
are
used
for
more
severe
dryness.
The
ring
contains
a low
dose
of
estrogen
and
may
not
protect
against
osteoporosis.
It
also
must
be
changed
every
3 months.
Mood
swings
- Lifestyle
behaviors,
including
getting
enough
sleep
and
being
physically
active
- Relaxation
exercises
- Antidepressant
or
anti-anxiety
drugs
Insomnia
- Over-the-counter
sleep
aids
- Milk
products,
such
as
a glass
of
milk
or
cup
of
yogurtchoose
low-
or
fat-free
varieties
- Do
physical
activity
in
the
morning
or
early
afternoon exercising
later
in
the
day
may
increase
wakefulness
- Hot
shower
or
bath
immediately
before
going
to
bed
Memory
problems
- Mental
exercises
- Lifestyle
behaviors,
especially
getting
enough
sleep
and
being
physically
active
|
Back to Top
Postmenopausal
Use
Menopause
may cause other changes
that produce no symptoms
yet affect your health.
For instance, a woman's
risk of developing
heart disease begins
to rise around menopause.
After menopause,
women's rate of bone
loss increases. The
increased rate can
lead to osteoporosis,
which may in turn
increase the risk
of bone fractures,
usually after age
70.
Through
the years, studies
were finding evidence
that estrogen might
help with some of
these postmenopausal
health risks especially
heart disease and
osteoporosis. With
more than 40 million
American women over
age 50, the promise
seemed great.
Although
erroneously thought
of in the past as
a "man's disease," heart
disease is the leading
killer of American
women. Women typically
develop it about
10 years later than
men.
Similarly,
menopause is a time
of increased bone
loss. Bone is living
tissue. Old bone
is continuously being
broken down and new
bone formed in its
place. With menopause,
bone loss is greater
and, if not enough
new bone is made,
the result can be
weakened bones and
osteoporosis, which
increases the risk
of breaks. One of
every two women over
age 50 will have
an osteoporosis-related
fracture during her
life.
Many
scientists believed
these increased health
risks were linked
to the postmenopausal
drop in estrogen
produced by the ovaries
and that replacing
estrogen would help
protect against the
diseases.
Box
5
|
About
Dietary
Supplements
If
you use
dietary
supplements
to try
to ease
hot flashes
and other
menopausal
symptoms,
you should
bear
these
points
in mind:
The U.S.
Food
and Drug
Administration
(FDA)
does
not have
the authority
to approve
dietary
supplements
before
they
are marketed,
and it's
important
to tell
your
health
care
provider
that
you are
taking
such
remedies.
Dietary
supplements
are sold
over
the counter
and may
contain
phytoestrogens:
These
are estrogen-like
substances
that
come
from
some
plants
(such
as soy)
and plant
materials
(such
as legumes,
vegetables,
cereals,
and some
herbs).
For instance,
these
products
may contain
black
cohosh,
wild
yams,
dong
quai,
and valerian
root.
Dietary
supplement
manufacturers
are responsible
for making
sure
that
their
products
are safe.
The FDA
must
show
that
a dietary
supplement
is harmful
before
it can
limit
the product's
use or
remove
it from
the market.
Currently,
there
are no
FDA regulations
that
specifically
establish
minimum
standards
for the
manufacture
of dietary
supplements
in order
to insure
their
identity
(tests
to insure
that
the ingredient
is actually
what
its label
claims),
purity,
quality,
strength,
and composition.
You may
want
to contact
a product's
manufacturer
before
buying
it.
Furthermore,
the possible
effects
of the
products
are not
known.
Some
of the
substances
they
contain
are being
studied.
For example,
soy contains
plant
estrogens,
which
are being
studied
to see
if they
have
the same
risks
and benefits
as estrogen.
Some
of this
research
is being
supported
by the
Office
of Dietary
Supplements,
the National
Center
for Complementary
and Alternative
Medicine,
the National
Institute
on Aging,
and other
units
of the
National
Institutes
of Health.
Until
more
is known
about
these
substances,
you should
use them
with
caution.
Also,
as noted,
tell
your
health
care
provider
if you
take
a dietary
supplement
or if
you increase
your
intake
of dietary
phytoestrogens.
There
may be
dangerous
side
effects.
An increase
in the
level
of estrogens
in your
body
could
interfere
with
other
prescription
medications
you are
taking
or even
cause
an overdose.
|
Back to Top
Early
Findings
Early
studies seemed to
support hormone therapy's
ability to protect
women against the
diseases that tend
to occur after menopause.
For instance, research
showed that the treatment
does prevent osteoporosis.
However, other findings
lacked evidence or
were unclear. No
large clinical trials
had proved that hormone
therapy prevents
heart disease or
fractures. Answers
also were needed
about other possible
effects of long-term
use of hormones,
especially on such
conditions as breast
and colorectal cancers.
Further,
prior research on
postmenopausal hormone
therapy's effect
on heart disease
had involved mainly
observational studies,
which can indicate
possible relationships
between behaviors
or treatments and
disease, but cannot
establish a cause-and-effect
tie. (See
Box 6 for more
about types of studies.)
Box
6
|
What
We Lean
From
Different
Types
of Studies
Medical
researchers
conduct
many
types
of studies.
The reason
is that
the studies
yield
different
kinds
of information.
Together,
the studies
help
scientists
understand
health
and disease,
and how
to educate
people
so they
can lead
healthier
lives.
Three
main
types
are:
observational
studies,
clinical
trials,
and community
prevention
studies.
Each
type
is discussed
briefly
below:
Observational
studies follow
women's
medical
and
lifestyle
practices
but
do
not
intervene.
Such
studies
can
turn
up
possible
relationships
between
various
factors
and
health
or
illness.
Those
factors
include
population
traits,
ethnicity,
genetic
attributes,
and
behaviors.
For
instance,
researchers
can
track
women
who
do
and
do
not
take
postmenopausal
hormone
therapy.
The
results
may
show
that
the
hormone
users
have
fewer
heart
attacks.
But
the
results
cannot
conclude
that
hormone
therapy
reduces
the
risk
of
heart
disease.
Other
factors
may
have
played
a part.
For
instance,
compared
with
women
who
do
not
use
hormone
therapy,
those
who
do
are
often
healthier,
have
a higher
level
of
education
and
better
access
to
medical
care,
and
are
more
willing
to
follow
a prescribed
therapy.
Clinical
trials control
and
compare
specific
medical
interventions,
such
as
the
use
of
postmenopausal
hormone
therapy.
Women
on
an
intervention
are
compared
with
those
who
do
not
receive
the
treatment.
Researchers
try
to
control
all
of
the
experimental
conditions
so
that
any
difference
between
the
two
groups
can
be
tied
to
the
intervention.
The
most
rigorous
of these
investigations
is the
randomized,
controlled,
double-blinded
clinical
trial.
Women
are randomly
assigned
to the
study
groups
and,
in a
drug
trial
for instance,
neither
the women
nor the
researchers
typically
know
who is
receiving
an active
drug
and who
a placebo.
Further,
on average
women
in the
two groups
will
be similar
in age,
education,
health
at the
time
of entering
the trial,
and other
factors
that
may affect
the results.
These
trials
are considered
to be
the "gold
standard" among
types
of studies
because
they
yield
the most
reliable
information.
Clinical
trials
are often
done
to test
whether
a possible
relationship
uncovered
in an
observational
study
is in
fact
so. The
trials
help
establish
a causal
link
between
a treatment
and a
specific
medical
outcome,
such
as fewer
heart
attacks.
Community
prevention
studies explore
ways
to
encourage
people
to
adopt
healthier
behaviors.
|
There
also were some
clinical trials,
which are considered
the "gold standard" in
establishing a
cause-and-effect
connection between
a behavior or treatment
and a disease.
The most definitive
clinical trials
are those that
test the effects
of a treatment
on the disease
itself. But such
clinical trials
are time-consuming
and costly. Consequently,
early clinical
trials of postmenopausal
hormone use tested
the therapy's effects
on the risk factors
or predictors of
various diseases.
One of the most
important of these
early clinical
trials that tested
effects on risk
factors was the "Postmenopausal
Estrogen/ Progestin
Interventions Trial," or
PEPI. Supported
by the National
Heart, Lung, and
Blood Institute
(NHLBI) and other
units of the National
Institutes of Health
(NIH), PEPI tested
the effects of
four hormone regimens
(one estrogenonly
and three different
estrogen plus progestin
regimens) on key
risk factors for
heart disease and
bone mass. Begun
in 1987, it followed
875 healthy, postmenopausal
women, ages 45-64,
for 3 years. About
a third of the
women had had a
hysterectomy. Participants
included various
races but were
predominantly white.
Box
7
|
Risk
Factors
for Uterine
Cancer
There
are various
types
of uterine
cancer.
The most
common
is endometrial
cancer,
which
begins
in the
lining
(endometrium)
of the
uterus.
It is
often
referred
to as
uterine
cancer.
Key
risk
factors
for
uterine
cancer
are:
- Ageusually
occurs
after
age
50
- Endometrial
hyperplasiaan
increase
in
cells
in
the
lining
of
the
uterus
- Hormone
therapyusing
estrogen
without
progesterone
- Obesity
and
related
conditions
- Tamoxifentaken
to
prevent
breast
cancer
- Racewhite
women
are
more
likely
than
African
American
women
to
develop
uterine
cancer
- Colorectal
cancerthose
who
have
an
inherited
form
are
at
a higher
risk
of
developing
uterine
cancer
- Factors
that
increase
exposure
to
estrogennot
having
children,
starting
menstruation
at
an
early
age,
entering
menopause
late
|
Back to Top
PEPI's
results were
generally positive:
-
Each
of the hormone
regimens
reduced "bad" LDL
cholesterol
and raised "good" HDL
cholesterol,
although
estrogen-only
raised good
cholesterol
the most.
(LDL, or
low density
lipoprotein,
carries cholesterol
to tissues,
including
the arteries,
while HDL,
or high density
lipoprotein,
carries it
away, aiding
its removal
from the
body.)
-
All
hormone therapies
decreased
levels of
fibrinogen.
(High levels
of fibrinogen
allow blood
clots to
form more
readily,
thus increasing
the risk
of heart
disease and
stroke.)
-
On
the other
hand, a large
percentage
of those
who took
estrogen
alone had
a high rate
of overgrowth
of the uterine
lining and
other abnormalities.
This finding
stressed
the need
for women
with a uterus
to use estrogen
plus progestin
therapy.
The added
progestin
protects
women against
uterine cancer
(see
Box 7).
Box
8
|
Breast
Cancer
Risk
Factors
About
80 percent
of breast
cancer
cases
occur
after
age 50.
One of
every
eight
American
women
who live
to be
85 develops
breast
cancer.
Some
factors
increase
the risk
for breast
cancer.
However,
most
women
who develop
breast
cancer
do not
have
any of
the risk
factors.
Key
factors
that
increase
the
risk
of
developing
breast
cancer
are:
- Personal
historyif
you've
had
it
once,
you're
more
likely
to
develop
it
again
- Family
historyif
your
mother,
sister,
or
daughter
had
breast
cancer,
especially
at
an
early
age,
you're
more
likely
to
develop
it
- Other
breast
changes
(not
including
ordinary "lumpiness")such
as
atypical
hyperplasia
(an
irregular
pattern
of
cell
growth)
- Genetic
alterationschanges
in
certain
genes,
including
BRCA1
and
BRCA2
mutations
Other
factors
also
may
increase
the
risk
of
developing
breast
cancer.
These
include:
- Racewhite
women
are
more
likely
to
develop
it
than
African
American
or
Asian
women
- Estrogen
exposurerisk
is
somewhat
increased
for
those
who
began
menstruation
early
(before
age
12),
had
menopause
late
(after
age
55),
never
had
children,
or
took
hormone
therapy
for
long
periods
- Late
childbearinghaving
a first
child
after
about
age
30
- Radiation
therapyif
given
to
the
chest
more
than
10
years
ago,
especially
in
women
younger
than
age
30
- Breast
densitybreasts
with
a high
proportion
of
lobular
and
ductal
tissue,
which
is
dense
and
in
which
breast
cancers
usually
appear
- Alcoholic
beverage
consumption
|
PEPI
did not last long
enough to tackle
some crucial questions
about hormone therapy,
such as a possible
rise in breast
cancer risk (see
Box 8).
The
first clinical trial
to investigate the
effects of postmenopausal
hormone therapy directly
on diseases was the "Heart
and Estrogen-Progestin
Replacement Study," or
HERS, which began
enrolling participants
in January 1983.
HERS tested whether
estrogen plus progestin
would prevent a second
heart attack or other
coronary event. Altogether,
it involved 2,763
postmenopausal women,
average age 67, who
already had heart
disease. The women
received either estrogen
plus progestin or
a placebo for about
4 years. (A placebo
is a substance that
looks like the real
drug but has no biologic
effect.)
Back to Top
Box
9
|
WHI
Findings
On Estrogen
Plus
Progestin
Therapy
Compared
with
a placebo,
after
about
5 years
of use,
estrogen
plus
progestin
resulted
in:
Increased
risks
- 26%
increase
in
breast
cancer
- 41%
increase
in
strokes
- 29%
increase
in
heart
attacks
- Doubled
rates
of
blood
clots
in
legs
and
lungs
Increased
benefits
- 37%
less
colorectal
cancer
- 34%
fewer
hip
fractures
No
difference
|
Box
10 [skip to text version]
|
Estrogen
Plus
Progestin
Pills
vs. Placebo
Pills
The
rate
of the
following
medical
conditions
per 10,000
women
per year

|
Box
10 Text
Version
[skip
to graphical
version]
|
Estrogen
Plus
Progestin
Pills
vs. Placebo
Pills
The
rate
of the
following
medical
conditions
per 10,000
women
per year
| |
Placebo Pills
|
Estrogen
Plus
Progestin Pills
|
Breast
Cancer
|
30
|
38
|
Heart
Attack
|
30
|
37
|
Stroke
|
21
|
29
|
Total
Blood Clots
|
16
|
34
|
Hip
Fracture
|
15
|
10
|
Colorectal
Cancer
|
16
|
10
|
|
Findings,
released in 1998,
showed that those
on the hormone
therapy did not
have fewer fatal
or nonfatal heart
attacks. In fact,
the women's risk
for a heart attack
increased during
the first year
of hormone use,
declining thereafter.
HERS also showed
that the therapy
caused an increase
in blood clots
in the legs and
lungs.
More
recently, the "HERS
Follow-Up Study," which
tracked the women
for about 3 more
years, found no decrease
in heart disease
from use of estrogen
plus progestin therapy.
Back to Top
Box 11
|
What
Do the
Data
Really
Mean?
The
data
sound
scaryand
confusing.
A 41
percent
increase
in strokes.
A 34
percent
decline
in hip
fractures.
Which
is more
important?
The bad
news,
or the
good?
Either
way,
the percentages
sound
big.
So it's
good
to take
a moment
and check
out what
they're
really
saying.
There
are two
main
ways
to express
risk"relative
risk" and "absolute
risk." The
relative
risk
measures
and compares
the percent
change
in risk
of some
health-related
event
in a
population
that
has been
exposed
to some
agent
and another
that
has not.
The increase
(or decrease)
in absolute
risk
is an
estimate
of the
number
or proportion
of women
who will
(or will
not)
develop
a disease
when
exposed
to a
particular
agent.
Relative
risk
allows
scientists
to compare
data.
In the
WHI study,
for example,
scientists
wanted
to find
out the
relative
risk
of breast
cancer
in women
who had
and had
not been
exposed
to the
estrogen
plus
progestin
hormone
therapy.
After
about
5 years,
the study
had 166
cases
of breast
cancer
among
estrogen
plus
progestin
users,
compared
with
124 in
the placebo
group.
However,
there
were
more
woman
in the
hormone
group8,506,
compared
with
8,102
in the
placebo
group.
To be
able
to compare
data
from
the groups,
the cases
were
converted
into
rates
per 10,000
women
per year.
Thus,
the rate
of breast
cancer
in the
hormone
group
was 38
per 10,000
women,
compared
with
30 per
10,000
women
in the
placebo
group.
This
also
can be
expressed
as 38
divided
by 30
or 1.26.
Since
that
is 0.26
greater
than
an equal
risk
(or 1.00),
the women
on hormone
therapy
had a
26 percent
greater
chance
of developing
breast
cancer
than
non-users.
What
was the
increase
in absolute
risk
of developing
breast
cancer
for women
in the
WHI study?
On average,
in any
single
year,
0.08
percent
more
women
in the
hormone
group
developed
breast
cancer
than
women
in the
placebo
group.
This
means
that,
if a
group
of 10,000
women
takes
estrogen
plus
progestin
for a
year,
there
will
be 8
more
cases
of breast
cancer
among
the hormone
users
than
if they
hadn't
taken
the therapy.
Thus,
women
on the
hormone
therapy
have
only
a slightly
increased
absolute
risk
of breast
cancer
over
a year.
(See
Boxes 9 and 10 for
a summary
of the
relative
and absolute
risks
of breast
cancer
and other
conditions
for women
in the
estrogen
plus
progestin
study.)
But,
if you
count
up all
the added
cases
of breast
cancer,
heart
attacks,
strokes,
and blood
clots
in the
lungs
and subtract
the fewer
cases
of colorectal
cancer
and hip
fractures,
you'd
still
get about
100 extra
harmful
events
among
the 10,000
hormone
users
after
5.2 yearsthe
period
the study
ran.
Multiply
that
by 10
years
and millions
of women
and the
number
of cases
of adverse
effects
grows.
Remember
too that
reports
of increased
risks
do not
mean
you will
develop
breast
cancer
or another
condition
if you
have
been
using
the hormone
therapy.
Your
personal
and family
medical
history,
along
with
your
lifestyle
and other
influences,
play
a big
role
in your
chance
of developing
a disease.
|
The
Women's Health
Initiative
In
1991, the NHLBI and
other units of the
NIH launched the "Women's
Health Initiative" (WHI),
one of the largest
studies of its kind
ever undertaken in
the United States.
It consists of a
set of clinical trials,
an observational
study, and a community
prevention study,
which altogether
involve more than
161,000 healthy,
postmenopausal women.
The
observational study
is looking for predictors
and biological markers
for disease and is
being conducted at
more than 40 centers
across the United
States, while the
community prevention
study, which has
ended, sought to
find ways to get
women to adopt healthful
behaviors and was
done with the Federal
Government's Centers
for Disease Control
and Prevention.
Back to Top
WHI's
three clinical
trials, conducted
at the same U.S.
centers, are designed
to test the effects
of postmenopausal
hormone therapy,
diet modification,
and calcium and
vitamin D supplements
on heart disease,
osteoporotic fractures,
and colorectal
cancer risk.
Box
12
|
Risk
Factors
for Stroke
Main
risk
factors
are:
- High
blood
pressure
- Diabetes
- Cigarette
smoking
Other
risk
factors
include:
- Family
historystroke
appears
to
run
in
some
families,
whether
due
to
genetics
and/or
shared
lifestyle
- Heavy
consumption
of
alcoholic
beverages
- High
blood
cholesterol
- Menopause
|
The
postmenopausal
hormone therapy
clinical trial
has two parts.
The first involved
16,608 postmenopausal
women with a uterus
who took either
estrogen plus progestin
therapy or a placebo.
The second involves
10,739 women who
have had a hysterectomy
and are taking
estrogen alone
or a placebo.
The
estrogen plus progestin
trial used 0.625
milligrams of conjugated
equine estrogens
taken daily plus
2.5 milligrams of
medroxyprogesterone
acetate taken daily
(Prempro). Two key
reasons that that
combination was chosen
are: It is the mostly
commonly prescribed
form of the combined
hormone therapy in
the United States,
and, in several observational
studies, it had appeared
to benefit women's
health.
The
women in the WHI
estrogen plus progestin
study were aged 50
to 79. They enrolled
in the study between
1993 and 1998. Their
health was carefully
monitored by an independent
panel, called the
Data and Safety Monitoring
Board (DSMB).
Box
13
|
Risk
Factors
for Colorectal
Cancer
About
30,000
women
a year
die of
colorectal
cancerit
is the
third-leading
cause
of cancer
deaths
for women,
after
lung
and breast
cancers.
Factors that increase the risk of colorectal
cancer
include:
- Agerisk
increases
after
age
50
- Dieteating
a diet
high
in
fat
and
calories,
and
low
in
fiber
- Polypsthese
are
benign
growths
on
the
inner
wall
of
the
colon
and
rectum
- Personal
medical
historyhaving
had
cancer
of
the
ovary,
uterus,
or
breast;
also
having
had
colorectal
cancer
once
increases
the
chance
of
developing
it
again
- Family
medical
historyhaving
first-degree
relatives
(parents,
siblings,
or
children)
with
colorectal
cancer,
especially
at
a young
age;
risk
increases
even
more
if
many
family
members
have
had
colorectal
cancer
- Ulcerative
colitisa
condition
in
which
the
lining
of
the
colon
becomes
inflamed
|
The
study's main goal
was to see if the
therapy would help
prevent heart disease
and hip fractures.
Another goal was
to see if those
possible benefits
were greater than
the possible risks
from breast cancer,
endometrial (or
uterine) cancer,
and blood clots.
The
study was to have
continued until 2005.
However, it was stopped
in July 2002 because
the DSMB found an
increased risk of
breast cancer and
that, overall, risks
from use of the hormones
outweighed and outnumbered
the benefits. "Outnumbered" means
that more women had
adverse effects from
the therapy than
benefitted from it.
The key results are
shown in Boxes 9 and 10.
These
results show both
risks and benefits
from use of the estrogen
plus progestin therapy.
The key adverse effects
were more cases of
breast cancer, heart
attacks, strokes,
and blood clots.
The main benefits
were fewer hip and
other fractures and
cases of colorectal
cancer.
Back to Top
Box 14
|
Postmenopausal
Hormone
Therapy
and Ovarian
Cancer
Risk
Early
studies
of postmenopausal
hormone
therapy
found
inconsistent
results
about
its effect
on the
risk
of ovarian
cancer:
Some
reported
increased
risk
with
estrogen
use,
while
others
reported
no effect
or even
a protective
one.
Most
of those
studies
were
relatively
small
and did
not take
into
account
the key
risk
factors
for ovarian
cancer
(see
Box 15).
More
recently,
two large
observational
studies
have
indicated
that
long-term
estrogen
use increases
the risk
of ovarian
cancer.
It's
important
to keep
in mind
that
observational
studies
do not
prove
that
a treatment
causes
a disease
(see
Box 6).
The evidence
from
these
studies
is cautionary,
not definitive.
Here's
more
on the
studies:
- One
study
followed
211,581
postmenopausal
women
from
1982-1996.
Of
those,
44,260
had
used
estrogen-only
hormone
therapy;
the
rest
did
not
use
hormone
therapy.
None
of
the
women
had
had
a hysterectomy,
ovarian
surgery,
or
cancer.
Those
with
10
or
more
years
of
estrogen
use
had
an
increased
risk
of
dying
from
ovarian
cancerand,
while
the
risk
decreased
somewhat
long
after
use
was
stopped,
it
was
still
higher
than
that
of
women
who
had
never
used
estrogen-only
therapy.
- Another
study
followed
44,241
women
from
1979-1998.
It
found
that
estrogen-only
therapy
increased
the
risk
of
ovarian
cancer.
Women
who
used
estrogen
alone
for
10
or
more
years
had
an
80
percent
higher
risk
of
ovarian
cancer
than
women
who
had
never
used
the
hormone
therapy;
women
who
used
estrogen
alone
for
20
or
more
years
had
a 220
percent
higher
risk
than
women
who
had
never
used
hormone
therapy.
The study found no increased risk of ovarian cancer for users of
estrogen plus progestin. However, few women in the study had used
the combination therapy for more than 4 years.
More
research
is needed
to see
if estrogen
plus
progestin
affects
ovarian
cancer
riskand
on other
aspects
of postmenopausal
hormone
use.
For instance,
another
recent
study
found
that
estrogen
alone
or estrogen
plus
progestin
used
on a
sequential
basis
increased
the risk
for ovarian
cancer,
while
estrogen
plus
progestin
used
continuously
did not.
|
Additionally,
there was no increase
in deaths from
breast cancer or
from other causes.
Further, there
was no increase
in the risk of
endometrial cancer.
Here's more on
the findingsto
better understand
them, see "Putting
It All Together," as
well as Box 11:
-
Breast
cancer. The
increased
risk of
breast
cancer
appeared
after 4
years of
hormone
use. After
5.2 years,
estrogen
plus progestin
resulted
in a 26
percent
increase
in the
risk of
breast
canceror
8 more
breast
cancers
each year
for every
10,000
women.
Women who
had used
estrogen
plus progestin
before
entering
the study
were more
likely
to develop
breast
cancer
than others,
indicating
that the
therapy
may have
a cumulative
effect.
-
Heart
attack. For
heart attack,
the risk
began to
increase
in the
first year
of estrogen
plus progestin
use and
became
more pronounced
in the
second
year. After
5.2 years,
there were
29 percent
more heart
attacks
in the
estrogen
plus progestin
group than
in the
placebo
groupor
7 more
heart attacks
each year
for every
10,000
women.
Unlike
HERS, which
involved
women with
heart disease,
the increased
risk from
estrogen
plus progestin
did not
go back
down again.
-
Stroke. For
the first
time, estrogen
plus progestin
was shown
to cause
more strokes
in healthy
women. By
the end of
the study,
the estrogen
plus progestin
group had
41 percent
more strokes
than the
placebo groupor
8 more strokes
each year
for every
10,000 women.
-
Blood
clots. The
risk of
total blood
clots was
greatest
during
the first
2 years
of hormone
usefour
times higher
than that
of placebo
users.
By the
end of
the study,
it had
decreased
to two
times greateror
18 more
women with
blood clots
each year
for every
10,000
women.
-
Fractures. Estrogen
plus progestin
reduced hip
fractures
by 34 percentor
5 fewer hip
fractures
for every
10,000 women.
This is the
first solid
evidence
from a clinical
trial that
hormone therapy,
in helping
to prevent
bone loss
and osteoporosis,
protects
women against
fractures.
-
Colorectal
cancer. The
therapy
also lowered
the risk
of colorectal
cancer
by 37 percentor
6 fewer
colorectal
cancers
each year
for every
10,000
women.
This reduction
appeared
after 3
years of
hormone
use and
became
more significant
thereafter.
However,
the number
of cases
of colorectal
cancer
was relatively
small,
and more
research
is needed
to confirm
the finding.
Back to Top
Box
15
|
Risk
Factors
for Ovarian
Cancer
About
1 in
57 American
women
will
develop
ovarian
cancer.
Most
will
be over
age 50,
but younger
women
also
can develop
the disease.
Here
are some
factors
that
increase
or decrease
the risk
of ovarian
cancer:
Increases
risk
- Agerisk
increases
as
a woman
ages
- Family
history
of
ovarian
cancerhigher
risk
if
mother
or
sister
has
had
ovarian
cancer;
somewhat
higher
risk
if
other
relatives,
such
as
grandmother,
aunt,
or
cousin,
have
developed
ovarian
cancer
- Postmenopausal
hormone
therapymay
increase
risk
- Fertility
drugs
- Personal
history
of
breast
and/or
colon
cancer
Decreases
risk
- Oral
contraceptivesthe
longer
the
use,
the
lower
the
risk
may
be
and
the
decrease
may
last
after
use
has
ended
- Childbearing
and
breast-feeding
- Tubal
ligation
(sterilization)
or
hysterectomy
- Prophylactic
(to
prevent
or
protect)
oophorectomy
(surgery
to
remove
one
or
both
ovaries)
|
The
findings are important
for several reasons:
As a clinical trial,
they establish
a causal link between
use of the particular
hormone therapy
and its effects
on diseases. Further,
the findings finally
offer some firm
guidance to the
millions of American
women who have
a uterus and may
consider taking
the drugs6
million already
use a form of combination
therapy. And, the
results apply broadlythe
study found no
differences in
risk by prior health
status, age, or
ethnicity. The
findings do not
apply to postmenopausal
use of estrogen
alone. That arm
of the study, which
used 0.625 mg per
day of conjugated
equine estrogen
(Premarin), did
not have the same
increased breast
cancer risk and
continues.
However,
an observational
study, supported
by the NIH's National
Cancer Institute
(NCI), recently found
that estrogen-only
therapy appeared
to increase the risk
of ovarian cancer
(see
Box 14). But
other, similar studies
have not found such
an increased risk,
and the possible
relationship between
estrogen use and
ovarian cancer remains
unclear. WHI participants
were informed of
these findings, and
the results were
reviewed for their
significance to the
study's continuation.
Box
16
|
What
About
Birth
Control
Pills?
The
recent
findings
about
the risks
of long-term
postmenopausal
hormone
therapy
do not
apply
to use
of birth
control
pills,
which
have
not been
found
to increase
breast
cancer
risk.
There had been concern about the effect of birth control pills
on the
risk
of breast
cancer
because,
until
recently,
studies
had given
conflicting
results.
For example,
a 1996
analysis
of 54
small
studies
had found
a slight
increase
among
women
who were
or had
recently
used
oral
contraceptives.
But the
54 studies
differed
in quality
and some
included
oral
contraceptive
preparations
no longer
in use.
Other
studies,
such
as the
1986 "Cancer
and Steroid
Hormone" (CASH)
study,
had found
no increased
risk.
In
June
2002,
findings
of the "Women's
Contraceptive
and Reproductive
Experiences
Study" (also
called
the Women's
CARE
Study)
were
released
and showed
no increased
risk
of breast
cancer,
regardless
of length
of oral
contraceptive
use,
timing
of use,
age at
use,
or the
users'
risk
factors
for developing
breast
cancer.
The study,
supported
by the
NIH's
National
Institute
of Child
Health
and Human
Development,
involved
more
than
9,257
women
between
the ages
of 35
and 64.
The women
were
interviewed
about
their
contraceptive
use.
Oral
contraceptives
do pose
risks,
however:
Combination
oral
contraceptives
increase
the risk
of blood
clots.
Oral
contraceptives
should
not be
used
if you
are at
an elevated
risk
for blood
clots
because
of diabetes
or another
condition,
or if
you smoke.
Taking
oral
contraceptives
and smoking
increases
your
risk
for heart
attack
and stroke.
Oral
contraceptive
use has
benefits
too:
It can
reduce
the risk
of ovarian
cancer,
endometrial
cancer,
colorectal
cancer,
pelvic
inflammatory
disease
(an infection
that
can lead
to infertility),
and osteoporosis.
|
Back to Top
Putting
It All Together
How
can you sort through
the benefits and
risks and make a
good decision about
whether or not to
use postmenopausal
hormone therapy?
Here are several
points to help you
evaluate the findings:
First,
it's important to
know that, because
the study involved
healthy women, only
a small number of
them had either a
negative or positive
effect from estrogen
plus progestin therapy.
The
percentages describe
what would happen
to a whole populationnot
to an individual
woman. For example,
the increased risk
of breast cancer
for the women in
the WHI study who
were taking the estrogen
plus progestin therapy
was less than a tenth
of 1 percent each
year.
But
if you apply that
increased risk to
a large group of
women and over several
years, then the number
of women affected
becomes an important
public health concern.
As noted, about 6
million American
women take estrogen
plus progestin therapy.
That would translate
into nearly 6,000
more cases of breast
cancer every year and,
if all of the women
took the therapy
for 5 years, that
might result in 30,000
more cases of breast
cancer.
Box
17
|
Talking
With
Your
Doctor
It's
important
to be
involved
in your
health
care.
Ask questions
and express
your
concerns.
Here
are some
questions
that
may help
you talk
with
your
health
care
provider
about
hormone
therapy:
- Why
am
I taking
hormone
therapy?
Or
why
should
I take
hormone
therapy?
- Which
hormone
therapy
am
I on?
- What
are
my
risks
for
heart
disease,
breast
cancer,
and
osteoporosis?
- Should
I stop
taking
the
hormone
therapy?
- What's
the
best
way
for
me
to
stop?
What
side
effects
will
I have?
- Is
there
an
alternative
therapy
that
I can
use
long-term?
- What
alternatives
can
help
me
prevent
heart
disease?
- What
alternatives
can
help
me
prevent
osteoporosis?
- What
can
I do
to
keep
menopausal
symptoms
from
returning?
Your
risk
for heart
disease,
osteoporosis,
and colorectal
cancer
may change
over
time.
So remember
to regularly
review
your
health
status
with
your
doctor
or other
health
care
provider.
It's also important to bear in mind that your
doctor
or other
health
care
provider
may not
be able
to answer
all of
your
questionsmany
questions
about
postmenopausal
hormone
use remain.
For instance,
it's
not yet
known
if increases
in disease
risk
caused
by long-term
use of
estrogen
plus
progestin
drop
after
use stops.
As with
any treatment,
you need
to carefully
weigh
your
personal
risks
against
the possible
benefits
and make
the best
choice
possible
for your
health
and lifestyle
needs.
Finally,
your
doctor
or other
health
care
provider
can speak
with
a WHI
Principal
Investigator
about
the study's
results.
For a
list
of the
Principal
Investigators,
check
the NHLBI
WHI Web
site
or contact
the NHLBI
Health
Information
Center.
|
Back to Top
Second,
bear in mind that
percentages aren't
fate. Whether expressing
risks or benefits,
they do not mean
you will develop
a disease. Many
factors affect
that likelihood,
including your
lifestyle and other
environmental factors,
heredity, and your
personal medical
history.
Finally,
realize that most
treatments carry
risks and benefits.
No one can make a
treatment choice
for you. Talk with
your doctor or other
health care provider
and decide what's
best for your health
and quality of life.
Begin by finding
out your personal
risk profile for
heart disease, stroke,
breast cancer, osteoporosis,
colorectal cancer,
and other conditions
(see Boxes 7, 8, 12, 13, 15, 18,
and 20).
Discuss quality of
life issues and alternatives
to postmenopausal
hormone therapy. Box
17 will help
you talk with your
health care provider.
Then weigh every
factor carefully
and choose the best
option for your health
and quality of life.
And keep the dialogue
goingyour health
status can change
and so can your choice.
Box
18
|
Your
Heart
Disease
Risk
Profile
One
in three
American
women
dies
of heart
disease.
Heart
disease
kills
more
American
women
than
any other
cause.
It also
can lead
to disability
and decrease
one's
quality
of life.
Yet,
many
women
don't
take
the threat
of heart
disease
seriously.
But menopause is a time when you need to get very
serious
about
heart
disease
because
that's
when
your
risk
for it
starts
to rise.
So, it's
more
important
than
ever
to talk
with
your
health
care
provider
about
how to
lower
your
risk
of heart
diseaseor,
if you
already
have
it, to
keep
it under
control.
Ask about
your "heart
disease
profile," a
check
of the
heart
disease
risk
factors
you already
have
or are
at an
increased
risk
of developing.
Risk
factors
are behaviors
or conditions
that
increase
your
chance
of developing
a disease.
The more
risk
factors
you have,
the greater
your
chance
of developing
the disease.
For heart
disease,
the risk
factors
don't
just
add their
risksthey
multiply
them.
So it's
vital
to prevent
them
or, if
you already
have
any,
to keep
them
under
control.
Fortunately,
most
heart
disease
risk
factors
can be
prevented
or controlled.
Here's
a breakdown
of both
types:
Risk
factors
beyond
your
control
- Being
age
55
or
older
- Having
a family
history
of
early
heart
diseasethis
means
having
a mother
or
sister
who
has
been
diagnosed
with
heart
disease
before
age
65,
or
a father
or
brother
diagnosed
before
age
55
Risk
factors
you
can
control
- Cigarette
smoking
- High
blood
cholesterol
- High
blood
pressure
- Diabetes
(high
blood
sugar)
- Overweight/obesity
- Physical
inactivity
|
Back to Top
Advice
About Postmenopausal
Hormone Therapy
While
many questions remain,
the new WHI findings
provide the basis
for some advice about
the use of postmenopausal
hormone therapy.
Here it is, along
with advice for short-term
hormone use to relieve
menopausal symptoms:
Short-term
estrogen alone or
estrogen plus progestin
therapy
-
"Short-term" means
the shortest
time needed
to manage
menopausal
symptoms.
The benefits
of such use
could outweigh
any risks
for you.
Most women
use the hormone
therapy for
2 to 3 years.
However,
some may
require a
longer period
of treatment.
Talk with
your health
care provider
about your
personal
risks and
needs.
Long-term
estrogen plus progestin
therapy
-
Do
not use estrogen
plus progestin
therapy to
prevent heart
disease.
The new findings
show that
it doesn't
work. In
fact, the
therapy increases
the chance
of a heart
attack or
stroke. And
it increases
the risk
of breast
cancer and
blood clots.
What can you do instead? Talk to your health care provider about other
ways to prevent heart disease and stroke that have been proven to be
safe and effective. These include lifestyle changes and such drugs
as cholesterol-lowering statins and blood pressure medications. Lifestyle
changes include: not smoking, maintaining a healthy weight, being physically
active, and managing diabetes.
Another key part of this is to follow a healthy eating plan that has
a variety of foods and is low in saturated fat and cholesterol and
moderate in total fat. In addition, limiting how much salt and other
forms of sodium you eat will help keep your blood pressure at a healthy
level.
-
Do
not use long-term
postmenopausal
hormone therapy
if you already
have heart
disease.
Such use
increases
the risk
of blood
clots. It
also increases
the risk
of heart
attack in
the first
year of therapy.
-
To
prevent osteoporosis,
talk with
your health
care provider
about what
your personal
risks and
benefits
would be
from estrogen
plus progestin
therapy.
Weigh any
benefits
against your
risk of heart
disease,
stroke, and
breast cancer.
Ask about
alternate
approaches
that are
considered
safe and
effective
in preventing
osteoporosis
and fractures.
These include
oral biphosphonates,
such as alendronate
(or Fosamax)
and risedronate
(or Actonel),
and selective
estrogen
receptor
modulators
(SERMs),
such as raloxifene
(or Evista).
SERMs are
also known
as designer
estrogens.
They are
substances
that have
estrogen-like
effects on
some tissues
and anti-estrogen
effects on
others.
Other steps to prevent osteoporosis include consuming enough calcium
and vitamin D (see Box 19), being physically active,
especially with weight-bearing exercises (such as walking, jogging,
playing tennis, and dancing), not smoking, and limiting how many alcoholic
beverages you drink. Smoking and drinking alcohol increase your risk
of osteoporosis. For more on osteoporosis, see Box
20.
Back to Top
Box
19
|
Recommended
Daily
Intakes
of Calcium
and Vitamin
D
|
|
Age
|
Vitamin
D
|
Calcium
|
19-50
|
200
IU*
|
1,200
mg**
|
51-70
|
400
IU*
|
1,200
mg**
|
70+
|
600
IU*
|
1,200
mg**
|
Note: IU=International Units
*
not to
exceed
2,000
IU
** not to exceed 2,500 mg
|
Long-term
estrogen-only therapy
General
advice
-
Whether
or not you
decide to
use postmenopausal
hormone therapy,
you should
keep your
regular schedule
of mammograms,
and breast
and clinical
exams.
-
In
addition
to having
regular mammograms,
you should
protect your
health by
having certain
other tests
done too
(see Box 21). These include tests for high blood pressure, high
blood cholesterol,
high blood
glucose (sugar),
bone mineral
density,
and overweight.
-
If
you stop
taking hormone
therapy and
your menopausal
symptoms
return, consider
alternative
treatments
(see
Box 4).
Be aware
that some
of these
remedies
have not
been proved
effective
or safe.
Back to Top
Box
20
|
Boning
Up On
Osteoporosis
More
than
8 million
American
women
have
osteoporosisand
millions
more
have
lost
so much
bone
that
they're
likely
to develop
it.
Osteoporosis
can happen
at any
age but
the risk
grows
as you
get older.
The first
noticeable
sign
of osteoporosis
is often
losing
height
or having
a bone
break
easily.
Other
signs
can be
changes
in the
shape
of the
spine,
prolonged
severe
pain
in the
middle
of the
back,
and tooth
loss.
Risk
factors
of
osteoporosis
include:
- Agerisk
increases
as
you
grow
older
- Being
a womanwomen
have
less
bone
tissue
and
lose
bone
faster
than
men
- Body
sizesmall,
thin-boned
women
are
at
greatest
risk
- Ethnicitywhite
and
Asian
women
are
at
highest
risk
- Family
historyhaving
parents
with
a history
of
fractures
- Sex
hormonesabnormal
absence
of
menstrual
periods
(amenorrhea)
or
menopause
- Anorexia
- Lifetime
diet
low
in
calcium
and
vitamin
D
- Certain
medications,
such
as
glucocorticoids
(prescribed
for
various
diseases,
including
arthritis,
asthma,
and
lupus)
or
some
anticonvulsants
- Physical
inactivity
or
extended
bed
rest
- Cigarette
smoking
- Excessive
use
of
alcoholic
beverages
If you
think
you're
at risk
for osteoporosis
or if
you're
menopausal
or older,
you may
want
to ask
your
doctor
or other
health
care
provider
about
having
a test
called
a DXA-scan
(dual-energy
x-ray
absorptiometry).
It measures
spine,
hip,
or total
body
bone
mineral
density,
or how
solid
bones
are.
The results
can show
the presence
and severity
of osteoporosis,
or if
you're
at risk
of developing
it or
having
fractures.
You
can prevent
osteoporosis.
The key
steps
are to
follow
an eating
plan
that's
rich
in calcium
and vitamin
D and
be sure
to get
regular
weight-bearing
exercises.
Calcium
and vitamin
D intake
can be
taken
as supplements
but check
with
your
health
care
provider
first.
Too much
of either
can cause
problems.
Recommended
daily
intakes
of calcium
and vitamin
D are
given
in Box
19.
Good
food
sources
of calcium
include
lowfat
dairy
foods,
canned
fish
with
bones,
such
as salmon
and sardines,
dark-green
leafy
vegetables,
such
as broccoli,
kale,
and collards,
calcium-fortified
orange
juice,
and breads
made
with
calcium-fortified
flour.
Vitamin
D is
made
by the
bodybeing
in the
sun 20
minutes
a day
helps
most
women
make
enough.
But it's
also
found
in eggs,
fatty
fish
(such
as sardines,
mackerel,
and salmon),
and cereal
and milk
fortified
with
vitamin
D. Weight-bearing
exercisesdone
three
to four
times
a weekthat
help
prevent
osteoporosis
include
walking,
jogging,
stairclimbing,
weight
training,
tennis,
and dancing.
It's
also
important
not to
smoke
and to
limit
how many
alcoholic
beverages
you drink.
Smoking
causes
the body
to make
less
estrogen,
which
protects
bones.
Too much
alcohol
can put
you at
risk
for falling
and breaking
bones.
Osteoporosis
is treated
by stopping
bone
loss
with
lifestyle
changes
and medication.
Hormone
therapy
has been
used
to prevent
and treat
osteoporosis.
But other
drugs
are available:
- Raloxifene
is
a SERM.
It
may
cause
hot
flashes
and
blood
clots.
- Alendronate
(brand
name
Fosamax)
and
risedronate
(brand
name
Actonel)
are
bisphosphonates,
drugs
that
slow
the
breakdown
of
bone
and
may
increase
bone
density.
Side
effects
may
include
nausea,
heartburn,
and
pain
in
the
stomach.
- Calcitonin
is
a naturally
occurring
non-sex
hormone
that
increases
bone
mass
in
the
spine.
It
is
used
for
women
who
are
at
least
5 years
beyond
menopause
and
is
taken
by
injection
or
nasal
spray.
The
injection
may
cause
an
allergic
reaction
and
has
some
unpleasant
side
effects,
including
flushing
of
the
face
and
hands,
urinating
often,
nausea,
and
skin
rash.
The
nasal
spray
may
cause
a runny
nose.
|
Back to Top
How
Do I Stop Postmenopausal
Hormone Therapy?
You
should talk with
your health care
provider about whether
or not stopping postmenopausal
hormone therapy would
be good for you.
Also ask about the
best way to discontinue
the treatment. You
can stop abruptly
or by gradually reducing
the dose over several
months.
However,
by abruptly stopping
the medication, you
may have menopause-like
symptoms. Gradually
weaning your body
off the medication
can ease this.
Box
21
|
Check
It Out
Here's a prescription for better health:
- Blood
pressurehealthy
women
should
have
it
checked
every
2 years;
others
may
need
it
checked
more
often.
- Lipoprotein
profilechecks
blood
levels
of
LDL,
HDL,
total
cholesterol,
and
triglycerides;
healthy
women
should
have
it
once
every
5 years.
- Blood
glucosetests
blood
levels
of
glucose
(a
sugar)
and
indicates
risk
for
diabetes;
healthy
women
age
45
| |