Researchers: new drug for osteoporosis shows promise
June 6, 1997
Web posted at: 12:08 a.m. EDT (0408 GMT)
WASHINGTON (CNN) -- A new class of drugs that mimics the
female hormone estrogen may help protect women's bones from
osteoporosis without increasing the risks of heart disease
and cancer, researchers say.
Preliminary results indicate the drug raloxifene, one in the
class of drugs called Selective Estrogen Receptor Modulators
can increase bone mass, which women begin losing at an
accelerated rate after menopause, according to a news release
from the Duke University Medical Center.
More than 25 million Americans, most of them elderly women,
are afflicted with the often crippling bone disease, which
can lead to debilitating, even deadly, fractures in the hip
and spine.
Interim results from a five-year global study of 12,000 women
show raloxifene increased bone density by 1 percent to 2
percent among 2,000 women with normal or slightly abnormal
bone mass. By contrast, women who took a placebo with calcium
supplements lost bone mass over the same two-year period.
"We start to see a compound that looks like it has estrogen's
benefits -- to the bones and to the heart and cardiovascular
system -- without its risks to the uterus and uterine
cancer, and to the breast and breast cancer," said Dr.
Kristine Harper of Duke University, one of 150 U.S. sites
participating in the research.
Still, raloxifene was not as effective as the hormone
estrogen, which can increase bone mass by 5 percent to 6
percent over a two-year interval. Hormone-replacement therapy
is often used to help prevent bone-thinning, but it can have
risks.
Raloxifene also appears to lower so-called bad cholesterol
(LDL) levels, as well as total cholesterol levels, which
could reduce the chance of heart disease and stroke,
researchers said.
The most commonly reported side effect of raloxifene was hot
flashes; these affected 24 percent of patients compared to 18
percent of those taking the placebo.
The research was presented Thursday at the Fourth
International Symposium on Osteoporosis: Research Advances
and Clinical Applications.
Correspondent Eugenia Halsey contributed to this report.
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