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Stress could increase risk of heart disease in women
REDUCED ESTROGEN levels due to stress may put some young women on
a high-risk course for heart disease, reported researchers from
Wake Forest University Baptist Medical Center at a meeting of the
North American Menopause Society.
"Our study of female monkeys indicates that stress affects
estrogen levels and can lead to the development of heart disease
- even before menopause," said Jay Kaplan, professor of
comparative medicine.
Kaplan said the women have traditionally been considered "immune"
from heart disease until after menopause, when their estrogen
levels dramatically drop. His research showed that stress can
actually reduce estrogen levels much earlier in life and cause
the buildup of fatty deposits in the arteries that can lead to
heart attacks and strokes.
"This research demonstrates that a deficiency of estrogen before
menopause places these females on a high-risk trajectory,
regardless of whether they get estrogen treatment after
menopause," said Kaplan. "Our data and recent trials in humans
suggest that the emphasis in this country on postmenopausal
estrogen treatment may be misplaced."
In the study, female monkeys were placed in groups so they would
naturally establish a pecking order from dominant to subordinate.
Monkeys that were socially stressed - because they were in
subordinate roles in their group - produced reduced amounts of
the hormone estrogen. In women, the estrogen produced before
menopause helps protect against heart disease and osteoporosis.
Kaplan's results showed that the estrogen-deficient monkeys had
four times more atherosclerosis than dominant monkeys that
produced normal levels of estrogen. When the subordinate, or
"stressed," monkeys got estrogen treatments either before or
after menopause, their rates of atherosclerosis were cut in half.
When they got a "double dose" of estrogen - both before and after
menopause - their rates of atherosclerosis were equal to the
dominant monkeys.
"Applied to women, this lifetime study suggests that having an
estrogen deficiency in the pre-menopausal years predicts a higher
rate of heart disease after menopause, even when treated with
hormone replacement therapy after menopause," said Kaplan. An
ongoing study of human autopsy results supports Kaplan's
findings. Results released last year showed that by age 35, one-
third of women have substantial atherosclerosis in the vessels
leading to their hearts.
In women, stress, anorexia nervosa and hormone imbalances can all
reduce estrogen levels to the point that menstrual periods stop.
But Kaplan and colleagues theorize that more moderate drops in
estrogen - that don't produce symptoms - can also affect health.
"We know from monkey studies that stress can lower estrogen
levels to the points that health is affected, even though the
animals still have menstrual periods," he said.
In a study of 66 women having normal-length menstrual periods,
estrogen levels were low enough in half of the participants to
cause the bone loss that can lead to osteoporosis. Kaplan
theorises that if reduced estrogen levels can cause bone loss in
women, they can also cause atherosclerosis. In Kaplan's monkey
study, estrogen was given in the form of oral contraceptives
prior to menopause. After menopause, it was given as hormone
replacement therapy. Monkeys were selected for the study because
they closely resemble humans in behavioural and reproductive
characteristics. The cynomolgus macaques, used in the study, have
a 28-day menstrual cycle and the females (except stressed
subordinates) have a natural resistance to heart disease compared
to males.
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