The Economist 14Dec2019

(lily) #1

52 International The EconomistDecember 14th 2019


2 popular. In America before 2001 some 20%
of post-menopausal women used it at
some point. By then a synthetic form of
progesterone was being administered
alongside oestrogen; it had been shown to
protect women from an increased risk of
uterine cancer caused by giving oestrogen
on its own.
The benefits of hrtseemed clear. Most
immediately, it offered relief from the mis-
erable symptoms of menopause. In the
longer term it reduced the risk of osteopo-
rosis (which rises after menopause) and
therefore the risk of bone fractures. Wom-
en liked that it seemed to stop their skin
thinning (probably because it boosts the
levels of collagen, a protein). It was thought
to reduce the risk of cognitive decline. But
most importantly, studies suggested that it
prevented the onset of cardiovascular dis-
ease—one of the biggest killers of women.

The great hormone scare
By 1997 a report in the Journal of the Ameri-
can Medical Associationconcluded that hrt
extended life expectancy for post-
menopausal women by as much as three
years. It had become a standard treatment.
But then a bombshell dropped.
In 2002 the results of a large random-
ised trial conducted by America’s National
Institutes of Health, known as the Wom-
en’s Health Initiative (whi), were rushed
into publication. It concluded that taking
oestrogen with synthetic progesterone in-
creased women’s risk of breast cancer,
heart attacks, strokes and blood clots.
Women were told that the dangers of hrt
mostly outweighed any benefits.
This finding overturned decades of
medical practice. As a final kicker, it
emerged that Mr Wilson had received mon-
ey from Wyeth-Ayerst, a company that
made oestrogen, while writing his pro-
hormone book. hrtwent from wonder-
drug to killer pill peddled by profit-hungry
pharmaceutical firms. Within six years
fewer than 5% of American post-meno-
pausal women were taking it. In Western
countries use of hrtincreased rapidly dur-
ing the 1990s but halved in the early 2000s.
To this day doctors are reluctant to pre-
scribe hormones to their patients.
But the first conclusions of the whi
study, on which so much antipathy to hrt
is still based, were almost entirely wrong.
The study had hoped to look at strategies
for preventing heart disease, cancer and
osteoporosis in post-menopausal women.
Avrum Bluming, an oncologist and co-au-
thor of a recent book, “Oestrogen Matters”,
says that instead of recruiting healthy
women in their late 40s and early 50s, who
were entering menopause, the median age
was 63. These older recruits were already
unhealthy. Half were obese. Nearly 50%
were current or past smokers and more
than a third had been treated for high blood

pressure. The women included in the study
probably suffered from atherosclerosis—
where plaque builds up inside arteries and
makes heart disease more likely—when it
began, says Mr Bluming. What the analysis
in 2002 actually showed was that offering
older and more unhealthy women hrtwas
a bad idea. It said nothing about the women
at whom the treatment was aimed.
There were other problems. The whi
study almost completely excluded from
the trial women who were experiencing
menopausal symptoms, fearing that those
given the placebo would abandon the trial
when their symptoms were not relieved.
But these are the women who would be ex-
pected to benefit most from the preventive
effects of hrt. Recent research suggests
that hot flushes and night sweats are asso-
ciated with an increased risk of heart attack
and stroke.
It is now clear that the long-term bene-
fits of hrtfor women given it as they enter
menopause are significant. A careful re-
analysis of the studies showed that women
in their 50s were actually 31% less likely to
die in the five to seven years that they were
taking hormones. For women who have
had their uterus removed or who start
menopause before the age of 45, it is life-
saving, preventing osteoporosis and heart
disease for as long as 18 years. There is a tiny
increase in the rates of breast cancer
among hrt-users after five years of the
treatment. This was lower than the risk
from working as a flight attendant.
A study published in the Lancet, a Brit-
ish medical journal, earlier this year has re-
ignited controversy over the level of risk of
breast cancer that comes with hormone
therapy. But Ms Davis and others worry that
its conclusions are not reliable. Moreover
any increase in risk must be weighed
against that of developing other diseases.
Taking hrt reduces the mortality of
women aged 50-59 by at least 20% and as

much as 40%, mostly because they suffer
fewer heart attacks. One in 25 of all women
will die of breast cancer; one in three will
die of coronary heart disease; and one in
six will die of a stroke. Around 90% of
women with breast cancer survive it in rich
countries. If women are on hrtat the time
of their breast-cancer diagnosis they are
less likely to die from the disease. Weigh-
ing such risks is part of the decision about
whether to embark on a course of hrt.
In addition to the flaws in the structure
of the whistudy, a change in the versions
of hormones used in hrt explains the
shifting scientific consensus on the treat-
ment’s effects. The synthetic form of pro-
gesterone used in the whiprobably trig-
gered cardiovascular problems. The
progesterone that many women now take
with an oestrogen supplement is thought
less likely to do so.
No long-term clinical trials of this spe-
cific combination of hormones have been
carried out. But, in theory, it should bring
all the benefits of oestrogen found in the
whitrial, with none of the risks of taking
synthetic progesterone.
In the absence of such studies, hrtre-
mains in medical limbo. And so women in
their late 40s and early 50s are losing out.
The window of opportunity to begin hrtin
order to capture its full benefits—includ-
ing resisting the effects of cognitive de-
cline—may be as little as two or three years.
Lucy’s symptoms worsened after her
doctor brushed her off. Convinced by her
online research that she was transitioning
into menopause, she paid to have blood
tested. The results confirmed her suspi-
cions that her hormone levels were the
problem. She was prescribed personalised
amounts of three hormones: an oestrogen
patch, micronised progesterone and tes-
tosterone. Within three days her hot
flushes had stopped, she was sleeping
peacefully and her mood had returned to a
happy equilibrium. She felt “superhuman”.
But her happy ending is less common
than it should be. In Britain more than 1m
women are thought to be missing out on
treatment. Elsewhere, the prevalence of
hrtis even lower. In Hungary and Russia
just 3% of menopausal women receive it. In
the absence of prescribed hormone thera-
py, some women turn to natural potions
which may alleviate the symptoms of
menopause but will not reduce a woman’s
future risk of a heart attack. Some types of
black cohosh, a popular herbal supple-
ment, have been associated with liver poi-
soning. In countries such as China, Japan
and Singapore, Chinese traditional medi-
cines are used. A diet rich in phytoestro-
gens, such as soya, may reduce the symp-
toms of menopause. This may explain why
East Asian women suffer less. But nothing
works as well as hrt. By shunning it, some
women are harming themselves. 7
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