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Posts Tagged ‘hormones’

Breast Cancer Incidence Drops in U.S.

Posted by medconsumers on January 15, 2009

The incidence of breast cancer in postmenopausal women has been decreasing since 2002, probably because so many women have given up hormone therapy, say researchers who assessed the follow-up data from the Women’s Health Initiative. This is the landmark trial that was that stopped early in 2002 because the women taking the combination estrogen plus progestin showed a higher incidence of heart disease, stroke, and breast cancer than the women taking placebos. Many of them stopped taking hormones immediately, and all were followed up until 2005.

The authors of this report said they are fairly confident that the falling breast cancer incidence was caused by the decreased use of hormones, not by the other opt-proposed possibility—the drop in the number of American women going for screening mammograms. One question remains: Why did the decline in breast cancer incidence occur so rapidly after the trial was stopped? The authors speculate that some of the tiny “pre-clinical cancers” found during mammography spontaneously regressed once women stop taking hormones.

N Engl J Med 2009;360:573-87

Posted in Cancer, Women's Health | Tagged: , | Comments Off

“Natural” Postmenopausal Hormones: Not so natural, not so safe

Posted by medconsumers on May 1, 2007

When a landmark clinical trial reported in 2002 that the dangers of postmenopausal hormone drugs far outweighed the benefits, many more women turned to bioidentical or natural hormones. These products are widely portrayed in the media and on the Internet as safer than prescription hormone drugs like Prempro and Premarin for the relief of hot flashes and other menopausal symptoms. The idea that these products are safer or even natural is challenged in a paper by Adriane Fugh-Berman, MD, and Jenna Bythrow of the Complementary and Alternative Medicine Master’s Program, Georgetown University School of Medicine.

Sold as topical creams and tablets over the Internet and in health food stores, bioidentical hormones are actually synthetic versions of female hormones, including estriol, estrone, estradiol, progesterone, testosterone, DHEA, thyroxine and cortisol. In their paper published recently in the Journal of General Internal Medicine, Fugh-Berman and Bythrow contend that bioidentical is a meaningless term coined by a business that knows what sells.

Compounding Pharmacies

Many of these products are prepared by compounding pharmacies that convert prescription and non-prescription drugs into different formulations. For example, converting a drug manufactured in tablet form to a syrup for people who have difficulty swallowing pills or a pet-sized dose of a drug meant for humans. In the case of bioidentical hormones, the pharmacies are reformulating the standard prescription hormone drugs, usually in weaker doses.

Because compounding pharmacies are not manufacturing facilities, they are not required by the FDA to prove safety or effectiveness. “Compounding pharmacies have their place,” said Dr. Fugh-Berman in a telephone interview. “But [with bioidentical hormones] all these pharmacies are doing are buying hormones from Upjohn or some other drug company and following a recipe.”

“Bioidentical hormones are chemically identical to hormones produced by the body,” explained Dr. Fugh-Berman, but the term bioidentical is widely misunderstood. Most women surveyed at one compounding pharmacy either thought it meant “not man-made” or plant-derived; they no doubt got that impression from advertising and/or reading the product labels which often, for example, feature wild yams as the source of progesterone.

Bioidentical hormones are sometimes derived from starting materials of plants in a lab process, Dr. Fugh-Berman said, “but, you won’t get progesterone from eating a yam. Plants have precursors in them, but not actual progesterone.”

Because compounding pharmacies are unregulated, they can make unsubstantiated claims for their products. (Legislation has been introduced.) The most dangerous to Dr. Fugh-Berman are the claims that bioidentical hormones will prevent heart disease and breast cancer, as well as improve well-being—all of which have been discredited for standard hormone drugs in the landmark 2002 Women’s Health Initiative trial.

Also, women with an intact uterus must protect it against estrogen-induced endometrial cancer with the addition of progesterone. Studies show that many bioidentical progesterone products contain much weaker doses of the standard progesterone prescription drugs, so they do not provide the level of needed protection.

For the many women who do not want to hear her message and will continue taking bioidentical hormones no matter what, Dr. Fugh-Berman has this advice, “Now we know that [the conventional prescription] hormones help only symptoms—hot flashes and vaginal dryness—they don’t prevent disease,” she said, referring to the results of the 2002 Women’s Health Initiative trial. “So symptomatic women should take the lowest possible dose for the shortest period of time. Women without symptoms shouldn’t use either bioidentical or conventional hormones for disease prevention. Bioidentical hormones should be assumed to have the same risks as conventional hormone drugs and should carry the same warning labels.”

As for the standard claim that bioidentical hormones are natural, “Ironically, the estrogen in the best-selling hormone preparations Premarin, Prempro, and Premphase is derived from pregnant mare’s urine, an inarguably natural source.”

Maryann Napoli, Center for Medical Consumers ©
May 2007

Posted in Alternative Medicine, Women's Health | Tagged: , | Comments Off

Hormones Cause Urinary Incontinence

Posted by medconsumers on March 1, 2005

Hormones Can Worsen and Cause Incontinence

For several decades, doctors have been prescribing estrogen to older women with urinary incontinence. But new findings show that hormones worsen the symptoms. What’s more, they increase the risk of healthy women becoming incontinent.

This is the latest bad news from the Women’s Health Initiative (WHI), the large clinical trial that had randomly assigned over 27,000 healthy postmenopausal women, aged 50 to 79 years, to take either hormones or placebos. The trial received enormous international media attention in 2002 when it had to be stopped prematurely due to a higher incidence of serious conditions among the women taking hormones. Among them were: more cases of breast cancer, heart disease, stroke, blood clots, and dementia. These harms greatly outweighed the two benefits—a reduced risk of colon cancer and fractures—shown among the women on hormones.

Researchers continue to comb through the “goldmine” of data produced by this trial. Gynecologist Susan L. Hendrix, DO, Wayne State University School of Medicine, Detroit , and colleagues looked at the incidence of incontinence in WHI participants after one year of taking hormones or placebos. They found an increase in all forms of urinary incontinence among the women who took hormones, compared with those on placebos.

The risk was highest for the most common form called stress incontinence, which is characterized by leaking of urine when coughing, sneezing, laughing, and/or exercising. Women on hormone therapy were also more likely to report that urinary incontinence had limited their daily activities. The WHI is the first randomized trial to show that women on estrogen alone were more likely to be incontinent than women who did not take hormones. Until the WHI, the incontinence risk was thought to be confined to women taking combination hormones.

This study was published in the February 23, 2005 issue of JAMA, the Journal of the American Medical Association. The WHI was a government-funded study so an extensive account of the results is available at www.whi.org

Maryann Napoli, Center for Medical Consumers ©
March 2005

Posted in Chronic Conditions, Women's Health | Tagged: , , | Comments Off

Two New Books about Hormones

Posted by medconsumers on July 1, 2003

Two New Books that take a Critical Look at Hormone Therapy
By Maryann Napoli
(July 2003)

The bad news about postmenopausal hormones came in increments. In July 2002, the Women’s Health Initiative trial was stopped prematurely because the estrogen/progestin combination drug called Prempro was-over a five-year period-causing more diseases than it was preventing. Then eight months later, the WHI produced another unexpected finding: hormone drugs aren’t all that helpful to women taking them to alleviate hot flashes.

In time, widely advertised hopes that estrogen could prevent Alzheimer’s disease were dashed when the WHI showed that the women taking Prempro had a higher rate of this much-feared disorder. And if that weren’t bad enough, last month a study involving one million British women found a substantially higher rate of breast cancer deaths among those had taken combination hormones than those who did not or those who took estrogen alone (The Lancet, 8/9/03).

So many questions remain. Why were gynecologists unanimously convinced that long-term hormone “replacement” therapy would prevent heart disease? Why were the adverse effects shown only for combination hormones and not estrogen alone? Are there any safe and effective alternatives for women who were taking hormones to alleviate menopausal symptoms? Two new books provide some answers.

For Susan M. Love, MD, the much admired breast surgeon, the underlying question that the WHI raises for her is why women need to replace hormones in the long term. Women require high levels of hormones to reproduce, she says, then they shift down to lower levels for the second half of life. In her latest book, Dr. Susan Love’s Menopause & Hormone Book, written with Karen Lindsey (New York: Three Rivers Press, 2003), Dr. Love notes that the marketing of hormone “replacement” therapy went hand in hand with the idea that once menopause begins, a heart attack or hip fracture will soon follow. Diseases of aging, like heart disease and osteoporosis, were reclassified as diseases caused by menopause. Both were portrayed as estrogen-deficiency diseases.

In The Greatest Experiment Every Performed on Women: Exploding the Estrogen Myth (NewYork: Hyperion, 2003), journalist Barbara Seaman writes that many women injured by hormones were bullied by their doctors into taking estrogen that they didn’t want or need; now many of them are being bullied by lawyers who also may not know what they are doing. In her 1969 ground-breaking book The Doctors’ Case Against the Pill, Seaman almost single-handedly started the women’s health movement when she brought public attention to the serious, sometimes fatal, health risks associated with oral contraceptives because the products sold in the 1960s had more than ten times the amount of hormones needed to prevent pregnancy.

The Greatest Experiment starts 65 years ago when a British biochemist published his formula for a cheap and powerful oral estrogen. Within months, writes Seaman, thousands of doctors and scores of drug companies around the world were working with this formula, prescribing it to slow and prevent aging, to stop hot flashes, to avoid pregnancy or miscarriage, and as a morning-after contraceptive. The risks of these drugs were known and documented from the start, according to Seaman, whose research shows that the British doctor who published his estrogen formula in 1938 spent many years warning that, though these drugs had great promise, they also put women at serious peril. He would become the first of several doctors to warn about giving hormones to healthy women.

Seaman, whose aunt died of estrogen drug-induced endometrial cancer, takes us through the subsequent decades of early failed attempts to study estrogen’s safety and efficacy as a contraceptive; the widespread prescription of the synthetic estrogen called DES to prevent miscarriage (it couldn’t, but that didn’t stop its use); the marketing of estrogen as an anti-aging panacea; and then brings the reader right up to recent years when healthy women were told to take estrogen to prevent heart disease and hip fractures. The injuries and deaths that occurred along the way did not seem to deter doctors and drug companies, nor did the lack of evidence to support the broad range of health claims. (Research has proven estrogen to be safe and effective only for alleviating symptoms of natural and surgical menopause.)

Seaman provides a behind-the-scenes view of the effectiveness of the women’s health activists who can be credited for-among many other things-getting written information about side effects, warnings, etc. mandated for all hormone drugs. When Wyeth-Ayerst asked the FDA to approve its estrogen drug Premarin for the prevention of heart disease, no professional medical society objected to the request. It was Cindy Pearson of the National Women’s Health Network who was the most vigorous dissenter. She successfully pressured the FDA to have the written information include the fact that estrogen has never been proven to prevent heart disease.

At a 1996 FDA meeting about the perennial fight to have written information with all prescription drugs, Seaman managed to get the then head of the AMA to admit publicly why his organization has been so adamantly against the idea. Dr. Roy Schwartz conceded Seaman’s points-that the provision of written information for hormone drugs had saved lives and reduced malpractice suits. Almost half of all prescriptions are written for conditions that are unproven, he explained. Doctors don’t want their patients to know they are getting a drug for [what is called] an off-label use, continued Dr. Schwartz, adding that people might sue their doctors for an injury incurred by a drug prescribed off-label.

While Seaman’s book provides the historical perspective that should make any reader into an educated skeptic once the next “miracle” drug comes along, Love’s book takes on the question of what menopausal women can do now that the all-purpose menopausal drug has been knocked from its pedestal. There are lots of options for women who want to prevent diseases of aging without resorting to estrogen, she writes, offering five chapters on non-drug approaches to symptom relief, as well as lifestyle changes. Some women suffer so severely from night sweats and hot flashes that they are willing to risk taking the drug for a year or so. Love provides easy-to-understand ways of weighing risks, not only of taking the combination hormones but also of developing the diseases of aging. In the WHI, taking estrogen alone, a choice available only to women without a uterus, appears to be safe-for now. This is the only group of participants allowed to continue to the trial’s originally intended end in 2006. As new research becomes available, Love advises women to be prepared to reevaluate their decisions.

One way for drug companies to sell mid-life women on the idea of lifelong hormone therapy was to sell fear of a potentially fatal hip fracture. Never mind that the odds of this occurring before age 70 are pretty slim. (Ironically, the WHI provided the first scientific evidence that combination hormones actually can reduce the rate of hip fracture.) Osteoporosis moved into the female collective consciousness in the 1980s. The chief culprit was purportedly loss of estrogen. What was once a risk factor (bone loss) has been turned into a disease, writes Love. Not so long ago, a woman did not have osteoporosis unless she had a fracture. A panel of international experts redefined osteoporosis as “a disease characterized by low bone mass and microarchitectural deterioration of bone tissue, which lead to increased bone fragility and a consequent increase in fracture risk.”

This greatly expands the number of people who now have a disease, writes Love, who observed that doctors and drug companies have focused women solely on the first half of that definition-low bone density. However, some researchers have found that bone architecture, or bone strength, is a far better determinant of who will suffer a hip fracture. No test can accurately measure bone strength so doctors test what they can-bone density-and continue to rely on dual-energy X-ray absorptiometry (DEXA). This test, suggested for all women over age 60 in osteoporosis ads by Merck, the maker of an osteoporosis drug, has caused many women to be diagnosed with what Love thinks is a made up condition. Osteopenia (reduced bone mass) is not a disease and not even a risk factor, she writes, and should not be treated. However, a DEXA-produced diagnosis of osteopenia led many a woman to an estrogen prescription.

Both books are written by women who have been at the vortex of the estrogen controversy for many years. Both authors are high-profile activists long known to have women’s best interests at heart.

Posted in Book Reviews, Cancer, Drugs, Heart, Women's Health | Tagged: , , , , , , , , , , , , , | Comments Off

Postmenopausal Hormones: A Cautionary Tale

Posted by medconsumers on August 1, 2002

Post Menopausal Hormones: A Cautionary Tale
By Maryann Napoli

Always read the information that comes with your prescription drug. That’s the take-home message from the recent announcement that postmenopausal hormones cause more harm than good. The woman who took the time to wade through the multiple pages of tiny type in the “patient packet insert” included* within her estrogen/progestin prescription would not have been surprised at the recent news that this combination causes far more harm than good.

For well over a decade, there had been an informal consensus building among gynecologists who seemed to think that virtually all women should consider lifelong hormone therapy, primarily to prevent heart disease. It’s doubtful that many doctors took the time to explain the uncertain safety of combining estrogen with progestin or the iffy nature of the heart protective effects. But the patient packet insert that comes with Prempro, the most widely prescribed estrogen/progestin combination, contains the following information listed under Precautions: “A causal relationship between estrogen replacement therapy and reduction of cardiovascular disease in postmenopausal women has not been proven. Furthermore, the effect of added progestins on this putative [reputed] benefit is not yet known.” Yes, it could have been written in a jargon-free style, but the key information about the “unknowns” is there.

Estrogen was approved by the Food and Drug Administration in 1942 to alleviate the symptoms of menopause. Ironically, the whole point of adding progestin to the regimen was to overcome an adverse reaction to estrogen (an increased risk of endometrial cancer) that was identified 35 years later. Now the combination has been shown to be far more dangerous than estrogen alone.

The story of postmenopausal hormones provides yet another illustration of how long a drug must be in use before a full picture of its safety and effectiveness becomes clear. It also shows the importance of randomized clinical trials. The National Institutes of Health-sponsored trial, called the Women’s Health Initiative (WHI) is the first large study ever to compare hormones with a placebo. The 16,608 healthy participants, aged 50 to 79 years, had been randomly assigned to take Prempro or a placebo. Those who had had a hysterectomy were randomly assigned to take estrogen or a placebo.

The main part of the WHI was stopped three years short of its intended goal because the women taking Prempro showed a higher rate of heart attacks, breast cancer, stroke, and blood clots than the women taking the placebo. These risks showed up after only four years on the drug. Though the women taking Prempro had a decreased risk of colon cancer and fractures, these benefits were far outweighed by the harms. The WHI continues to study the women without a uterus who presently show no significant benefit or risk from taking estrogen alone.

You might wonder why the heart-protective benefit remained so fixed within the belief system of the average gynecologist. For example, a small increase in the number of heart attacks, strokes, and blood clots in the lungs showed up in the first one to two years of use of estrogen and progestin. But doctors reasoned that this small risk (less than 1% altogether) would disappear after two years, so the trial was allowed to continue. But, in the next years, the women on the hormone combination showed a continued increase in heart attacks, strokes, and blood clots. The same disturbing results showed up in an earlier randomized trial that explored the question of whether hormones could prevent heart attacks in women with heart disease.

But gynecologists, as a group, had managed to convince themselves that the heart benefits would eventually be verified. Previous trials did show estrogen’s good effect on what doctors call “markers” for heart disease, such as cholesterol. And there were many observational studies, indicating that women who took hormones had a lower incidence of heart disease. But upper-income women tend to have lower rates of heart disease, and this is the same group that was more likely to take hormones. As Susan M. Love, MD, author of Dr. Susan Love’s Hormone Book, is fond of saying, “We don’t know whether the hormones made the women in these observational studies healthy, or whether healthy women took hormones.” Definitive information did not arrive until the WHI announced its findings last month in the Journal of the American Medical Association (JAMA, 7/17/02).

The same issue of that journal included another study that reported an increased risk of ovarian cancer to be associated with the use of estrogen alone. The risk was especially relevant to women who took estrogen for ten or more years. This study, however, was not a randomized trial, so it is possible that the ovarian cancer risk will not be confirmed in future, well-designed clinical trials.

There are many women who take hormones solely for the purpose of alleviating menopausal symptoms or osteoporosis prevention. For these women, both pharmaceutical and non-pharmaceutical alternatives are described in one of the Web sites listed below.

Resources:
-Consult the Physicians’ Desk Reference, which is available at most community libraries, before taking any prescription drug. Though quite daunting in language and format, the PDR is the only source of accessible information for consumers who want the most complete information about any prescription drug they are about to take. The book is updated yearly and can be purchased at most major chain bookstores. The patient packet insert referred to in this article is the same information provided in the PDR. Unlike other drug reference books, the PDR describes what has been proven in terms of effectiveness in the pre-approval clinical trials and how long the trials followed the participants.

-For alternatives to hormone therapy, including supplements and other drugs, visit the Web site of the North American Menopause Society (www.menopause.org). NAMS has received funding over the years from Wyeth, makers of Prempro, Premarin, and other estrogen drugs, and it has been the prime force behind the inappropriate promotion of these drugs for prevention of heart disease. At this Web site you can also read the organization’s position papers and expert comments on the WHI findings.

-The Food and Drug Administration Web site (www.fda.gov) has prescription drug information, but it is better at providing it for newly approved drugs. If you can find your way to “advisory committee transcripts,” that is where the pre-approval discussions of a drug’s pros and cons can be found.

-Our Web site (www.medicalconsumers.org) grants free access to the March 2002 HealthFacts article on postmenopausal hormones.

*Hormone drugs are in a rare category of prescription drugs. Their manufacturers are mandated by law to include written information for consumers in their products. How well they comply has yet to be studied. To find this important information for all prescription drugs, see “Resources.”

(August 2002)

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Postmenopausal Hormones: An Update

Posted by medconsumers on March 1, 2002

Postmenopausal Hormones: An Update
by Maryann Napoli

Postmenopausal hormones have been promoted to women (and doctors) for nearly four decades with promises of everything from youthful skin to increased longevity. The currently popular indications-prevention of heart attack and hip fracture-are not supported by good research. Two large trials, which randomly assigned women to take hormones or not, have failed to confirm estrogen’s heart protective effects. And while many randomized controlled trials (RCTs) have proven estrogen’s ability to stop the loss of bone density, none lasted long enough to show that this hormone actually prevents fractures.

Estrogen is still prescribed to women as a treatment for osteoporosis (bone loss), though the Food and Drug Administration removed this indication in 1999 because of lack of evidence. Only one indication for taking hormones is backed up with good research support-the relief of menopausal symptoms, such as hot flashes.

The two large RCTs, which provided the heart-related results, are the Women’s Health Initiative (WHI) and the Heart and Estrogen/Progestin Study (HERS). Together they included about 30,000 participants. The HERS was designed to determine whether hormones can prevent heart attacks in women, aged 44 to 79 years, who have heart disease. And the WHI, which includes healthy women, aged 50-79 years, is exploring the effects of hormone therapy on the prevention of heart disease and osteoporosis-related fractures, and on the risk of breast and uterine cancers. All participants had been randomly assigned to take a placebo (inactive pill) or hormones (estrogen alone for women who had a hysterectomy or estrogen plus progestin for women with an intact uterus).

The data from these and other RCTs are being searched for information about a range of health effects associated with hormone therapy:

Cardiovascular Events: Both the HERS and the WHI found a small increase in the number of heart attacks, strokes, and blood clots in the lungs in the first one to two years of hormone use. Researchers initially thought that this small risk (fewer than 1% altogether) would disappear after two years, but longer follow-up showed otherwise. Last year, the WHI reported a continued increase in heart attacks, strokes, and blood clots in women taking hormones.

Prevention of Another Stroke: Among 652 women (mean age 71 years) who had suffered a non-disabling stroke or a transient ischemic attack, those who had been randomly assigned to take oral estradiol did not show a lower incidence of death or stroke. Worse, the rate of fatal stroke was significantly higher among those taking estradiol (a form of estrogen).

Fractures: The WHI is designed to answer the question of whether hormones prevent fractures, following its participants for eight to 12 years.

Urinary Incontinence: 1,525 women with urinary incontinence participated in the HERS. All were younger than 80 years and had experienced at least one episode of urinary incontinence per week. Incontinence improved in 26% who had been assigned to take a placebo for four years, as compared with 21% assigned to take hormones. Urinary incontinence worsened in 27% of the placebo group, as compared with 39% of the hormone group.

Dry Eye Syndrome: 665 participants of Women’s Health Study, a RCT that began in 1992, found a slight increased incidence of dry eye syndrome in hormone users (past and current), especially among the women on estrogen alone. According to questionnaires completed by the participants: 9% of those taking estrogen alone reported severe symptoms diagnosed by physician, as compared with 7% among the estrogen plus progesterone or progestin, and 6% among those who never used hormones. Dry eye syndrome, a condition with no effective treatment, can damage the surface of the eye.

Urinary Tract Infection: Women in the HERS who had been randomly assigned to take hormones for four years did not have a lower incidence of urinary tract infections.

Gallbladder Disease: The HERS showed gallbladder disease to be 38% higher among those who had been assigned to take estrogen/progestin therapy.

Annoying “Minor” Side Effects: Breast tenderness with uterine bleeding caused 30% to stop taking hormones by the end of one year.

What’s Wrong With Observational Studies?

Many benefits attributed to hormones, such as prevention of Alzheimer’s disease, have yet to be validated in an RCT. Such information comes from less reliable research, known as observational studies. Such research takes a backward look at women who chose to take hormones to determine whether their health status differs from that of women who did not take hormones.

The problem with observational studies is this: Women who take hormones tend to be upper income and well educated. Both characteristics are associated with better heart health and longevity. Susan Love, MD, author of Dr. Susan Love’s Hormone Book, identified the problem: “We don’t know whether hormones made the women healthy, or whether healthy women take hormones.” It is the observational studies that misled so many gynecologists to believe that estrogen prevents heart disease.

An RCT provides more trustworthy results because participants of similar age, health status, etc, are randomly assigned to take the drug or not. Then they are followed for years. Most RCTs are double-blind, which means that neither the participants nor the health professionals monitoring them know who is on the placebo and who is taking the active drug.

Benefits and Risks Yet to Be Confirmed:

Colorectal Cancer: Observational studies have produced inconsistent findings regarding the possibility that hormones lower the risk of colorectal cancer. The results range from no reduction to a 33% reduction in colorectal cancer.

Cognition: Observational studies suggest that hormone therapy may reduce the risk of cognitive decline. A systematic review of all studies, including some RCTs, that explored this topic was published last year in the Journal of the American Medical Association. The participants, who had been taking hormones for the symptoms of menopause, showed improvements in “verbal memory, vigilance, reasoning, and motor speed, but no enhancement in other cognitive functions.” The authors went on to explain that most of these studies had significant limitations.

Alzheimer’s Disease: No RCT has been conducted regarding the risk of dementia. Earlier observational studies suggest that women taking hormones were less likely to develop Alzheimer’s disease, but more recent observational studies did not find this benefit.

Breast Cancer: Does estrogen use increase the risk of developing breast cancer? More than 30 observational studies have been conducted to answer this question. But, here too, the results have been inconsistent. Some found estrogen use to be associated with a reduced risk of developing breast cancer; others found an increased risk of breast cancer beginning after five years of use. And some studies found no risk. The WHI has been designed to provide a reliable answer to the question of whether there is an association between estrogen and breast cancer.

Endometrial (uterine) Cancer: Ever since it became known that estrogen increases a woman’s odds of developing uterine cancer, the drug is now prescribed with another hormone, progestin, to women with an intact uterus. Not all doses of progestin protect the uterus, however. For the results of a review of all trials that determined appropriate doses, see “Protecting the endometrium” by Gibbons and Thorneycroft in the Journal of Reproductive Medicine (2/99).

For More Information About the WHI:

The Women’s Health Initiative is sponsored by the U.S. National Heart, Lung and Blood Institute. Visit its Web site at www.nhlbi.nih.gov/whi/hrt/htm for more information about the progress of this trial.

(March 2002)

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