Posted April 16, 2004
A large, multi-center heart disease prevention study, part
of the Women's Health Initiative (WHI), in which UAB participated, found that
estrogen-alone hormone therapy had no effect on coronary
heart disease risk but increased the risk of stroke for
postmenopausal women. The study also found that estrogen-
alone therapy significantly increased the risk of deep vein
thrombosis, had no significant effect on the risk of breast
or colorectal cancer, and reduced the risk of hip and other
fractures.
The WHI is sponsored by the National Heart, Lung, and Blood
Institute (NHLBI), part of the National Institutes of
Health (NIH).
The estrogen-alone study was stopped at the end of February
2004 because the hormone increased the risk of stroke and
did not reduce the risk of coronary heart disease, a key
question of the trial. The study was to have ended in March
2005. Initial findings appear in the April 14 issue of The
Journal of the American Medical Association.
A separate report on the WHI Memory Study of estrogen
alone's effects on dementia and cognitive function will be
published soon.
"These findings confirm that estrogen-alone therapy should
not be used to prevent chronic disease," said NHLBI Acting
Director Dr. Barbara Alving. "We believe the findings
support current FDA recommendations that hormone therapy
only be used to treat menopausal symptoms and that it be
used at the smallest effective dose for the shortest
possible time."
"The results make clear that hormone therapy does not
protect women against coronary heart disease and increases
their risk for stroke," said Dr. Jacques Rossouw, WHI
Project Officer at NHLBI. "This may be especially true for
older women, such as those aged 60 and older in this
study."
As of July 2003, about 10 million American women were
taking some form of hormone therapy. It is estimated that
about 6.7 million of those take estrogen alone and 3.3
million take estrogen plus progestin. The drugs tested in
the WHI are those most commonly used in the United States.
The estrogen-alone study involved 40 clinical centers and
10,739 generally healthy postmenopausal women ages 50-79
who did not have a uterus. Their average age at enrollment
was nearly 64 and about 70 when the study stopped. They
enrolled in the study between 1993 and 1998.
About 75% of the women were white, 15 percent black,
and 6 percent Hispanic. Most of the women were overweight
and about 8% had diabetes. About 35% of the
women had used hormone therapy in the past and about 13% were current users at the time they enrolled in the
study.
The women were randomized to two groups-one received 0.625
mg/day of conjugated equine estrogens (Premarin [TM]) and the
other a placebo. Premarin[TM] and the placebo were supplied by
Wyeth-Ayerst Research.
The women were followed for an average of 6.8 years. They
visited their clinic at least once a year, and had annual
mammograms and clinical breast exams.
The study was carefully monitored by an independent Data
and Safety Monitoring Board (DSMB). The NIH made the
decision at the beginning of February 2004 to stop the
study drugs. The JAMA article includes data collected
through February 2004.
For every 10,000 women each year, on average, estrogen-
alone use compared to placebo resulted in:
INCREASED RISK FOR:
- Stroke (fatal and non-fatal)
12 cases more (44 cases in those
on estrogen alone and 32 in those on placebo)
- Venous thrombosis (blood clot, usually in one of the deep
veins of the legs)
6 cases more (21 cases in those on estrogen alone and 15 in
those on placebo) (An increased risk of pulmonary embolism
- blood clots in the lungs -- was not statistically
significant -- there were 13 cases in those on estrogen
alone and 10 in those on placebo.)
NO DIFFERENCE IN RISK OR UNCERTAIN EFFECT FOR:
- Coronary heart disease
No significant difference in risk (neither increased nor
decreased) -- 5 fewer cases (49 cases in those on estrogen
alone and 54 in those on placebo). During the first two
years of use, risk was slightly increased for estrogen
alone, but it appeared to diminish over time.
- Colorectal cancer or total cancer
No significant difference in risk (neither increased nor
decreased) -- 1 more case for colorectal cancer and 7 fewer
cases for total cancer (for colorectal cancer, 17 cases in
those on estrogen alone and 16 in those on placebo; for
total cancer, 103 cases in those on estrogen alone and 110
in those placebo)
- All deaths or those for a specific cause
No significant difference in risk (neither increased nor
decreased) -- 3 more deaths (for all deaths, 81 in those on
estrogen alone and 78 in those on placebo)
- Breast cancer
Uncertain effect -- 7 fewer cases (26 cases in those on
estrogen alone and 33 in those on placebo). This finding
was not statistically significant.
INCREASED BENEFIT FOR:
Bone fractures
6 fewer hip fractures (11 cases in those on estrogen alone
and 17 cases in those on placebo)
The results above were not affected by race or ethnicity,
or body mass index (BMI).
The combined hormone therapy study involved 16, 608
participants, who were randomly assigned to receive either
a daily intake of 0.625 mg of conjugated equine estrogens
plus 2.5 mg of medroxyprogesterone (Prempro[TM]), or a
placebo. Combination therapy is used when women have a
uterus to prevent the development of endometrial cancer.
Key findings of estrogen plus progestin compared to the
placebo for every 10,000 women each year were: more strokes
(8 more cases); an increased risk of breast cancer (8 more
breast cancers); an increase in heart attacks (7 more heart
attacks); a higher risk of blood clots (8 more women with
blood clots in the lungs and 18 more with blood clots in
the legs or lungs); a reduction in hip fractures (5 fewer
hip fractures); and a drop in the risk of colorectal cancer
(6 fewer colorectal cancers).
Rossouw cautioned that the findings for the two hormone
therapy studies should not be compared directly. "At
baseline, the women in the estrogen-alone study had a
higher risk of cardiovascular disease than those in the
estrogen-plus-progestin trial. Those in the estrogen-alone
study were more likely to have such heart disease risk
factors as high blood pressure, high blood cholesterol,
diabetes, and obesity."
Women in both hormone trials are now in a followup phase,
due to last until 2007, during which their health will be
closely monitored.
WHI was launched in 1991 and consists of a set of clinical
trials to test the preventive effects of postmenopausal
hormone therapy, diet modification, and calcium and vitamin
D supplements on heart disease, fractures, breast and
colorectal cancer, as well as an observational study, which
is looking for predictors and biological markers for
disease. The diet modification trial involves nearly 49,000
women, the calcium/vitamin D trial about 36,000 women, and
the observational study about 94,000 women -- all three
studies are continuing.
Additional information on menopausal hormone therapy,
including the WHI estrogen-plus-progestin study, can be
found on the NIH Website at www.nih.gov
Other online sources of information are:
Women's Health Initiative www.nhlbi.nih.gov/whi