In male dogs, testosterone injections are used to treat urinary incontinence but are generally less effective than
estrogen therapy in female dogs.
Not exact matches
He was writing
in the wake of new revelations about
estrogen replacement
therapy that showed that the benefits of
estrogen had been vastly overstated.
Recently, Manson and colleagues published a long - term study of the risk of death
in women
in the two WHI hormone
therapy trials — combined
therapy and
estrogen alone — from the time of trial enrollment
in the mid-1990s until the end of 2014.
In 2004, researchers published results of the WHI study of
estrogen - only
therapy, taken for about seven years by women who had had their uteruses surgically removed.
However, along with this seemingly linear storyline
in which retinoids block progesterone's promotion of CK5 + cells, previous work
in the lab of CU Cancer Center investigator Peter Kabos, MD, and others shows that breast cancers treated with anti-
estrogen drugs like tamoxifen or aromatase inhibitors show an increased population of CK5 + cells — it is as if these
therapies remove the roadblock of
estrogen - dependent cells, leaving CK5 + cells to proliferate.
In other words, unfortunately, anti-
estrogen therapies may kill
estrogen - dependent cells but at the expense of spurring the growth of CK5 + cells.
Estrogens have been reported to exert protective vascular effects
in animal and observational but randomized clinical trials did not report such effects
in older women, even suggesting the possibility of an increased CVD risk
in this setting, especially with combined
estrogen plus progestin
therapy.
In 2001 the trend reversed: Breast cancer rates initially dipped gradually, but dropped sharply in mid-2002, when many women in the U.S. stopped hormone replacement therapy after the Women's Health Initiative, a large clinical trial involving estrogen - progestin therapy, was stopped after it was determined that the risks — most notably the increased likelihood of developing breast cancer — outweighed the benefit
In 2001 the trend reversed: Breast cancer rates initially dipped gradually, but dropped sharply
in mid-2002, when many women in the U.S. stopped hormone replacement therapy after the Women's Health Initiative, a large clinical trial involving estrogen - progestin therapy, was stopped after it was determined that the risks — most notably the increased likelihood of developing breast cancer — outweighed the benefit
in mid-2002, when many women
in the U.S. stopped hormone replacement therapy after the Women's Health Initiative, a large clinical trial involving estrogen - progestin therapy, was stopped after it was determined that the risks — most notably the increased likelihood of developing breast cancer — outweighed the benefit
in the U.S. stopped hormone replacement
therapy after the Women's Health Initiative, a large clinical trial involving
estrogen - progestin
therapy, was stopped after it was determined that the risks — most notably the increased likelihood of developing breast cancer — outweighed the benefits.
Researchers at the Kaiser Permanente Center for Health Research
in Portland, Ore., concluded there is definitely a link between breast cancer and the use of menopausal hormone
therapy, particularly
estrogen - progestin treatment combinations.
Since the report that it did cause breast cancer and many women have stopped taking hormone replacement
therapy, we've seen a decrease
in breast - cancer incidence, exactly what you'd predict for our understanding of how
estrogens work.
Since being approved
in the U.S.
in the early 1940s,
estrogen and progestin
therapy has been widely used to ease menopausal symptoms as well as prevent many chronic diseases, such as osteoporosis and heart disease.
Estrogen therapy reduced some of the risk
in women who had undergone the procedure.
The drop
in hormone use dates back to July 2002, when the Women's Health Initiative, a 15 - year study tracking the health of more than 160,000 women, abruptly ended its long - term study of
estrogen - progestin hormone replacement
therapy because women taking the drugs faced an elevated risk of invasive breast cancer and heart disease.
More discouraging news about hormone replacement
therapy for menopausal women appeared
in June: Women taking Prempro, the most widely prescribed pill containing both
estrogen and progestin, are more likely to develop Alzheimer's and to have early breast tumors that go undetected by mammograms.
«This could be very applicable for women suffering from hot flashes or depression for whom
estrogen therapy is really counter-indicated,» says neuropharmacologist Roberta Brinton of the University of Southern California
in Los Angeles, who was not involved
in the new work.
A breast cancer
therapy that blocks
estrogen synthesis to activate cancer - killing genes sometimes loses its effectiveness because the cancer takes over epigenetic mechanisms, including permanent DNA modifications
in the patient's tumor, once again allowing tumor growth, according to an international team headed by the University of Pittsburgh Cancer Institute (UPCI).
Perhaps shedding light on this mystery, the researchers found three different types of mutations
in the
estrogen receptor
in patients whose cancer was resistant to anti-hormone
therapy.
Hot flashes are particularly severe and frequent
in breast cancer survivors, but current FDA - approved remedies for these unpleasant episodes, such as hormone replacement
therapies are off - limits to breast cancer survivors because they include
estrogen.
«Preclinical studies suggest a possible benefit of
estrogen therapy when combined with exercise to increase strength and performance and to prevent the loss of muscle mass, but the role of
estrogen in muscle mass is not yet clear for postmenopausal women,» says Dr. JoAnn Pinkerton, executive director of NAMS.
In June researchers from the Women's Health Initiative Memory Study added a dismal confirmation: estrogen - only replacement therapy in postmenopausal women who've had a hysterectomy not only fails to prevent memory loss but may also increase the risk of dementi
In June researchers from the Women's Health Initiative Memory Study added a dismal confirmation:
estrogen - only replacement
therapy in postmenopausal women who've had a hysterectomy not only fails to prevent memory loss but may also increase the risk of dementi
in postmenopausal women who've had a hysterectomy not only fails to prevent memory loss but may also increase the risk of dementia.
Hunt and colleagues exposed some newborn mice to BPA and some newborn mice to a synthetic
estrogen used
in birth control pills and hormone
therapy.
Gwendolyn Thomas, assistant professor of exercise science, is the co-author of a groundbreaking article
in the Obesity Journal (The Obesity Society, 2017) about the effects of exercise and physical activity on postmenopausal breast cancer survivors taking AIs — hormone -
therapy drugs that stop the production of
estrogen.
By contrast, women receiving
estrogen therapy had a smaller increase
in cortisol and showed no decrease
in working memory function.
Short - term
estrogen - progestin combination
therapy did not show an increase
in risk.
«These findings are unique
in showing a sustained effect over two years and that even
in older postmenopausal women breast density can increase
in response to
estrogen - plus - progestin
therapy,» McTiernan said.
This hypothesis is corroborated by animal studies showing that angiogenesis was negatively influenced by
estrogen loss
in oophorectomized animals (290), whereas
estrogen therapy induced collateral and microvascular remodeling
in a similar animal model (291).
It was used
in this study for the first time to study factors that cause
estrogen receptor positive breast cancer to recur during tamoxifen
therapy.
WASHINGTON (September 8, 2016)-- An animal study suggests that resistance to tamoxifen
therapy in some
estrogen receptor positive breast cancers may originate from
in utero exposure to endocrine disrupting chemicals.
Potential cardioprotection was based on generally supportive data on lipid levels
in intermediate outcome clinical trials, trials
in nonhuman primates, and a large body of observational studies suggesting a 40 % to 50 % reduction
in risk among users of either
estrogen alone or, less frequently, combined
estrogen and progestin.2 - 5 Hip fracture was designated as a secondary outcome, supported by observational data as well as clinical trials showing benefit for bone mineral density.6, 7 Invasive breast cancer was designated as a primary adverse outcome based on observational data.3, 8 Additional clinical outcomes chosen as secondary outcomes that may plausibly be affected by hormone
therapy include other cardiovascular diseases; endometrial, colorectal, and other cancers; and other fractures.3, 6,9
Now, all breast cancers are classified as
estrogen - receptor positive or negative, an important guide to prognosis and
therapy, and medications, such as tamoxifen, that can block the effects of
estrogen have become important tools
in the treatment and possible prevention of breast cancer.
Despite marked advances
in breast cancer
therapy, basal - like breast cancer (BBC), an aggressive subtype of breast cancer usually lacking
estrogen and progesterone receptors, remains difficult to treat.
These results, also presented at the 2015 European Cancer Congress (ECC2015, abstract # 5BA) today, which involve the group of 1,626 patients with a Recurrence Score between 0 and 10, demonstrated that 99.3 percent of node - negative,
estrogen receptor (ER)- positive, human epidermal growth factor receptor 2 (HER2)- negative patients who met accepted guidelines for recommending chemotherapy
in addition to hormonal
therapy, had no distant recurrence at five years after treatment with hormonal
therapy alone.
But Suzanne Somerss hormone
therapy — she takes bioidentical hormones, injects her vagina with a hormone called estriol, and rubs
estrogen or progesterone cream on her arms every day — has put her
in the limelight.
«
In the Womens Health Initiative (WHI) trial, when women got seven years of
estrogen alone, there was no increased risk of breast cancer, but after four to five years on combined hormone
therapy, the risk emerges,» she says.
Low doses of prescription medications, including antidepressants, can help relieve hot flashes
in overweight women who need immediate relief, Dr. Nachtigall says, as can hormone
therapy, which replaces
estrogen and other hormones that decline during menopause.
Research has shown that bioidentical
estrogen is important for both safety and improved effectiveness, which is why we only use bioidentical hormones
in estrogen replacement
therapy.
Estrogen therapy for women comes
in many different forms.
Testosterone and
estrogen receive the most attention
in the world of hormone replacement
therapy, but the action of progesterone may be just as important.
In a group of women 65 to 80 years of age who had never used hormone replacement
therapy of any kind, blood levels of estradiol (one of the human
estrogens) were measured.
For some men who have low testosterone levels that are not yet
in a dire state, progesterone
therapy with an aromatase blocker may help increase T while preventing the
estrogen conversion that can lead to
estrogen dominance and weight gain.
The same is observed
in estrogen replacement
therapy — the doses are generally all greatly excessive.
When you understand the role of
estrogen in the body, the benefits of
estrogen therapy become clear.
From L.A. Times Staff and Wire Reports June 6, 1995 Contrary to much current medical thinking, long - term use of hormone replacement
therapy may significantly increase the risk of breast cancer
in postmenopausal women, even when progestins are added to
estrogen, according to a new study.
Because when you consider your exposure over the course of a lifetime, it really adds up; the average American woman uses up to 16,800 tampons
in her lifetime — or as many as 24,360 if she's on
estrogen replacement
therapy.
Although bio-identical hormone
therapy seems to work for most post-menopausal women for arthritis relief, there are a few women that still have arthritis and arthralgias
in spite of the
estrogen cream.
Conventional synthetic
estrogen and progestin
therapy caused these side effects and «Bioidentical hormones» (which are identical to natural hormones present
in the body) are therefore touted as providing the same benefits without side effects.
Vaginal
estrogen therapy may also be used
in women who have breast, cervical or ovarian cancer, and medical consultation must be sought for proper advice on its risks and benefits.
Intake of calcium must be combined with
estrogen therapy to further decrease * rates of bone loss as
estrogen may help increase * the absorption of calcium
in the gut.
For these reasons, evaluation of hormone replacement
therapy in men should assess not only testosterone, but both free and conjugated
estrogens.
These articles will explain how to supplement with natural progesterone cream and bioidentical
estrogen, and why natural progesterone and
estrogen replacement
therapy can make a big difference
in a woman's health and quality of life.