MEDICATIONS: TIMING OF START OF HORMONE
THERAPY MAY HAVE EFFECT ON RISK OF CORONARY HEART DISEASE
April 13, 2007 — Women who initiate hormone therapy closer to menopause tend
to have a reduced risk of coronary heart disease compared to women who begin
treatment further from menopause, but researchers did not find this reduced risk
was statistically significant, according to a study in the April 4 issue of the
Journal of the American Medical Association.
Studies examining the effects of the use of postmenopausal hormone therapy on
coronary heart disease (CHD) have yielded mixed results, depending on the type
of study conducted. There may be a number of reasons for the differences,
including the timing of initiation of hormone therapy, according to background
information in the article. Jacques E. Rossouw, M.D., of the National Heart,
Lung, and Blood Institute in Bethesda, Md., and colleagues conducted a secondary
analysis of data from the Women's Health Initiative (WHI) trial to determine
whether the effects of hormone therapy on risk of cardiovascular disease varied
by age or years since menopause began. The WHI trial included 10,739
postmenopausal women who had undergone a hysterectomy who were randomized to
conjugated equine estrogens (CEE) or placebo and 16,608 postmenopausal women who
had not had a hysterectomy who were randomized to CEE plus medroxyprogesterone
acetate (CEE + MPA) or placebo. Women ages 50 to 79 years were recruited to the
study from 40 U.S. clinical centers between September 1993 and October 1998.
"Although not statistically significant, these secondary analyses suggest
that the effect of hormones on CHD may be modified by years since menopause and
by the presence of vasomotor symptoms [such as hot flashes or night sweats],
with higher risks in women who were 20 or more years since menopause (or aged 70
years or greater). Coronary heart disease tended to be nonsignificantly reduced
by hormone therapy in younger women or women with less than 10 years since
menopause, and the risk of total mortality was reduced in women aged 50 to 59
years," the authors write.
"We did not have adequate statistical power to assess outcomes in the women
aged 50 to 54 years or less than five years since menopause. As previously
reported, CEE appeared to be associated with lower risk of CHD than CEE + MPA.
Importantly, the risk of stroke was not influenced by years since menopause, the
presence of vasomotor symptoms, or drug regimen, although there was no increased
risk of stroke in women aged 50 to 59 years."
"The absence of excess absolute risk of CHD and the suggestion of reduced
total mortality in younger women offers some reassurance that hormones remain a
reasonable option for the short-term treatment of menopausal symptoms, but does
not necessarily imply an absence of harm over prolonged periods of hormone use.
In contrast, risk of stroke did not depend on years since menopause or the
presence of vasomotor symptoms. The findings are consistent with current
recommendations that hormone therapy be used in the short-term for relief of
moderate or severe vasomotor symptoms, but not in the longer term for prevention
of cardiovascular disease," the authors conclude.
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