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Menopause - Post WHI
                  Jessie Chan
               27th Sept 2012
Women’s Health
  Initiative
15 year project - 1991-2010

3 components:

   Randomized clinical trial
       68,132 postmenopausal women between the ages of 50-79.

       Hormone Therapy (HT): Effect of HT on the prevention of heart disease and osteoporosis, and
       any associated risk for breast cancer. Women participating in this component took hormone pills
       or a placebo (inactive pill).

       Dietary Modification: Effect of a low-fat, high fruit, vegetable and grain diet on the prevention of
       breast and colorectal cancer and heart disease. Study participants followed either their usual
       eating pattern or a low-fat eating program.

       Calcium/Vitamin D: Effect of calcium and vitamin D supplementation on the prevention of
       osteoporosis-related fractures and colorectal cancer. Women in this component took calcium and
       vitamin D pills or a placebo.

   Observational study
       examined the relationship between lifestyle, health and risk factors and specific disease outcomes

   Community prevention study
WHI - Hormone trial
Two studies
 The estrogen-plus-
 progestin study
 (women with a uterus)

 The estrogen-alone study
 (women without a uterus)
WHI - Hormone trial
Compared with the placebo,                     Compared with the placebo,
estrogen plus progestin resulted in:           estrogen alone resulted in:
   Increased risk of heart attack
                                                 No difference in risk for heart
   Increased risk of stroke                      attack
   Increased risk of blood clots
                                                 Increased risk of stroke
   Increased risk of breast cancer
                                                 Increased risk of blood clots
   Reduced risk of colorectal cancer

   Fewer fractures                               Uncertain effect for breast cancer

   No protection against mild cognitive          No difference in risk for colorectal
   impairment and increased risk of dementia
                                                 cancer
   (study included only women 65 and older)

                                                 Reduced risk of fracture

                                                 (Findings about memory and
WHI - Limitations
Addressed the value of long-term HT in the prevention of major chronic conditions of
women after menopause, not intended to explore treatment of menopausal symptoms.

E+P trial was stopped after 5.6 years because of an increased risk of breast cancer and
because overall risks, including increased risks for heart attack, stroke, and blood clots,
outnumbered benefits

The E-alone study was stopped after 6.8 years because of an increased risk of stroke and
no reduction in risk of CHD. The estrogen-alone study also found an increased risk of
blood clots.

Difference between results of E+P and E-alone, progestin (medroxyprogesterone
acetate) may be responsible?

 Two trials populations dissimilar - E-alone participants had a higher mean body mass
index and more years of prior exposure to HT than E + P participants, so interpretation
of trial differences must be cautious.
Recent Debates:
HRT and CVD
HRT and CVD
Women’s Health Initiative (WHI) (Rossouw et al, JAMA 2007; 297: 1465-77)

   Younger women (50 -59) taking HRT over a period of 10 years have shown no
   increased risk of developing CVD - previous WHI study which stated an
   opposite finding

The women's international study of long duration estrogen and progestin
after menopause (WISDOM)

   Women starting or restarting combined HRT have increased cardiovascular and
   thromboembolic risk when treatment begins many years after the menopause
   (Vickers et al, BMJ, July 2007, doi:10.1136/bmj.39266.425069.AD)

   Decreased risk of osteoporotic fracture and no difference in the risk of stroke or
   cancers.
Recent Debates:
HRT and Breast Ca
HRT and Breast Ca
Studies have shown an association between E+P with breast cancer - but related to certain
types of HRT and certain types of breast cancer for women of a particular age group.

The recorded risks are statistically small and appear to be linked with the duration of therapy
(Ravdin et al, NEJM 2007; 356: 1670-4)

Postmenopausal women who take E+P for at least 5 years are increasing their risk of breast
cancer. Researchers also found that women can quickly reduce their risk of breast cancer
by stopping HRT (Chlebowski et al., NEJM 2009; 360(6): 573-587).

In considering these findings, women should be aware that only a small percentage of
combined estrogen plus progestin users continue use for more than five years (Brett &
Reuben, Obstet Gynecol 2003; 102:1240-9).

The Society of Obstetricians and Gynaecologists of Canada has noted that risk factors for
breast cancer, such as hormones, should be evaluated in light of equally important risk
factors related to lifestyle (Reid et al, JOGC 2009; 31(1): S5-S8)

Research suggests that 34% of breast cancers could be avoided by making lifestyle
changes at the time of menopause (Sprague et al, Am J Epidemiol 2008; 168(4): 404-11).
Recent Debates:
HRT and Ovarian Ca
HRT and Ovarian Ca
Million Women Study - increased incidence of developing ovarian cancer in
women on HRT, compared to women who have never used HRT (Million
Women Study Collaborators, Lancet 2007; 369:1703-10). However, these
risks are statistically small. Researchers report that the risk of developing
ovarian cancer returns to pre-use levels once users stop using HRT.
Recent Debates:
HRT and Colon Ca
HRT and Colon Ca
Small reduction in the risk of colonic cancer (Johnson JR et al, Cancer
Epidemiology Biomarkers Prev 2009;18(1):196-203).

Evidence from the WHI and other trials suggests that current HRT users
have a 40% reduction in colorectal cancers.

? too early to consider HRT use in the prevention of colon cancer (Barnes
and Long)
Recent Debates:
HRT and VTE
HRT and VTE
There is an increased risk of venous thromboembolism with oral HRT. This
may be increased with age and obesity, and may vary by the progestogen
used. Observational studies suggest that it may not be associated with
transdermal HRTs (patches), but this needs confirmation (Archer and Ogar).
Recent Debates:
HRT and stroke
HRT and stroke
There is a modest increase in stroke risk with HRT use if stated near the
menopause. This risk rises considerably in women who start at older ages.
There is some evidence that use of HRT patches (as opposed to pills) may
not increase stroke risk, but this needs to be confirmed (Henderson and
Lobo).
Recent Debates:
HRT and bone
HRT and bone
Taking HRT confers some benefit to bone strength (Farquhar C et al,
Cochrane Database Syst Rev. 2009 Apr 15;(2):CD004143)

Fractures The WHI "Global Index", which looked at the balance of risks and
benefits, inappropriately downgraded the importance of fractures.

HRT gives more bone benefits than many other drugs (e.g.
bisphosphonates), and so restrictions on HRT use as a first-line therapy are
not appropriate (de Villiers and Stevenson)
HRT and UG + sexual
health
HRT and UG + sexual
health
Around 50% of postmenopausal women will suffer urogenital atrophy.
Studies indicate that locally applied hormone therapy is generally
more effective than systemic HRT for urogenital symptoms, including
dyspareunia, which can be a critical determinant of a woman’s
interest in sex.(Nappi & Davis)

E-P is effective for relief of lower urinary tract symptoms related to
estrogen deficiency

Most studies show that in post menopausal women with urinary
incontinence, E-alone and E-P are not beneficial and may worsen the
condition
Recent Debates:
HRT and QoL
HRT and QoL
WHI - HRT use led to minimal improvement in quality
of life

WHI study wasn’t designed to look at wemen going
through the menopause - underestimated the real
extent of effect of HRT on QoL - hence suffering to
many women

Some studies indicate that E-P improves many domain
of QoL - mental health and depressive symptoms,
physical functioning, bodily pain and sleep.
Recent Debates:
HRT and dementia
HRT and dementia
Initial WHI results showed an increase in dementia
for both E+P and E alone users.

  ? may be influenced by the timing of the HRT
  initiation, with benefits for those starting nearer
  the menopause, but increased risks for women
  starting at older ages (Maki and Henderson).
Current
recommendations
The risks associated with the use of HRT are low and duration of use may, if necessary, be
extended, as the use of HRT for many women provides welcome relief from distressing
postmenopausal symptoms (Grady & Barrett-Connor, BMJ 2007; 334:860-1).

Start early, use the lowest dose which gives symptom control, for the shortest period of time
(Benefit outweighs the risks)

‘window-of-opportunity' - before the age of 60 and/or within 10 years of the menopause.

    This reduces the risk of coronary heart disease and overall mortality. HRT is more effective
    for this than other medicines such as statins and aspirin, and is cost-effective. Starting HRT
    later than this increases risks to women (Hodis et al).

All women commencing HRT should be advised of type, dose, mode of delivery and
duration

Tailor treatment to individual patients
References
Effect of Hormone Therapy on Risk of Heart Disease May Vary by Age and
Years Since Menopause. Additional analyses from the Women’s Health
Initiative. NHI News April 2007

The Women’s Health Initiative study and Hormone Therapy – what have we
learned 10 years on? International Menopause Society. May 2012

Wallace, Robert. The Women’s Health Initiative: The Role of Hormonal
Therapy in Disease Prevention

Women’s Health Initiative. http://www.nhlbi.nih.gov/whi/

Hormone Therapy During Menopause in Malaysian Women. Clinical Practice
Guidelines July 2010.
Thank you....

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Menopause post WHI

  • 1. Menopause - Post WHI Jessie Chan 27th Sept 2012
  • 2. Women’s Health Initiative 15 year project - 1991-2010 3 components: Randomized clinical trial 68,132 postmenopausal women between the ages of 50-79. Hormone Therapy (HT): Effect of HT on the prevention of heart disease and osteoporosis, and any associated risk for breast cancer. Women participating in this component took hormone pills or a placebo (inactive pill). Dietary Modification: Effect of a low-fat, high fruit, vegetable and grain diet on the prevention of breast and colorectal cancer and heart disease. Study participants followed either their usual eating pattern or a low-fat eating program. Calcium/Vitamin D: Effect of calcium and vitamin D supplementation on the prevention of osteoporosis-related fractures and colorectal cancer. Women in this component took calcium and vitamin D pills or a placebo. Observational study examined the relationship between lifestyle, health and risk factors and specific disease outcomes Community prevention study
  • 3. WHI - Hormone trial Two studies The estrogen-plus- progestin study (women with a uterus) The estrogen-alone study (women without a uterus)
  • 4. WHI - Hormone trial Compared with the placebo, Compared with the placebo, estrogen plus progestin resulted in: estrogen alone resulted in: Increased risk of heart attack No difference in risk for heart Increased risk of stroke attack Increased risk of blood clots Increased risk of stroke Increased risk of breast cancer Increased risk of blood clots Reduced risk of colorectal cancer Fewer fractures Uncertain effect for breast cancer No protection against mild cognitive No difference in risk for colorectal impairment and increased risk of dementia cancer (study included only women 65 and older) Reduced risk of fracture (Findings about memory and
  • 5.
  • 6. WHI - Limitations Addressed the value of long-term HT in the prevention of major chronic conditions of women after menopause, not intended to explore treatment of menopausal symptoms. E+P trial was stopped after 5.6 years because of an increased risk of breast cancer and because overall risks, including increased risks for heart attack, stroke, and blood clots, outnumbered benefits The E-alone study was stopped after 6.8 years because of an increased risk of stroke and no reduction in risk of CHD. The estrogen-alone study also found an increased risk of blood clots. Difference between results of E+P and E-alone, progestin (medroxyprogesterone acetate) may be responsible? Two trials populations dissimilar - E-alone participants had a higher mean body mass index and more years of prior exposure to HT than E + P participants, so interpretation of trial differences must be cautious.
  • 7. Recent Debates: HRT and CVD HRT and CVD Women’s Health Initiative (WHI) (Rossouw et al, JAMA 2007; 297: 1465-77) Younger women (50 -59) taking HRT over a period of 10 years have shown no increased risk of developing CVD - previous WHI study which stated an opposite finding The women's international study of long duration estrogen and progestin after menopause (WISDOM) Women starting or restarting combined HRT have increased cardiovascular and thromboembolic risk when treatment begins many years after the menopause (Vickers et al, BMJ, July 2007, doi:10.1136/bmj.39266.425069.AD) Decreased risk of osteoporotic fracture and no difference in the risk of stroke or cancers.
  • 8. Recent Debates: HRT and Breast Ca HRT and Breast Ca Studies have shown an association between E+P with breast cancer - but related to certain types of HRT and certain types of breast cancer for women of a particular age group. The recorded risks are statistically small and appear to be linked with the duration of therapy (Ravdin et al, NEJM 2007; 356: 1670-4) Postmenopausal women who take E+P for at least 5 years are increasing their risk of breast cancer. Researchers also found that women can quickly reduce their risk of breast cancer by stopping HRT (Chlebowski et al., NEJM 2009; 360(6): 573-587). In considering these findings, women should be aware that only a small percentage of combined estrogen plus progestin users continue use for more than five years (Brett & Reuben, Obstet Gynecol 2003; 102:1240-9). The Society of Obstetricians and Gynaecologists of Canada has noted that risk factors for breast cancer, such as hormones, should be evaluated in light of equally important risk factors related to lifestyle (Reid et al, JOGC 2009; 31(1): S5-S8) Research suggests that 34% of breast cancers could be avoided by making lifestyle changes at the time of menopause (Sprague et al, Am J Epidemiol 2008; 168(4): 404-11).
  • 9. Recent Debates: HRT and Ovarian Ca HRT and Ovarian Ca Million Women Study - increased incidence of developing ovarian cancer in women on HRT, compared to women who have never used HRT (Million Women Study Collaborators, Lancet 2007; 369:1703-10). However, these risks are statistically small. Researchers report that the risk of developing ovarian cancer returns to pre-use levels once users stop using HRT.
  • 10. Recent Debates: HRT and Colon Ca HRT and Colon Ca Small reduction in the risk of colonic cancer (Johnson JR et al, Cancer Epidemiology Biomarkers Prev 2009;18(1):196-203). Evidence from the WHI and other trials suggests that current HRT users have a 40% reduction in colorectal cancers. ? too early to consider HRT use in the prevention of colon cancer (Barnes and Long)
  • 11. Recent Debates: HRT and VTE HRT and VTE There is an increased risk of venous thromboembolism with oral HRT. This may be increased with age and obesity, and may vary by the progestogen used. Observational studies suggest that it may not be associated with transdermal HRTs (patches), but this needs confirmation (Archer and Ogar).
  • 12. Recent Debates: HRT and stroke HRT and stroke There is a modest increase in stroke risk with HRT use if stated near the menopause. This risk rises considerably in women who start at older ages. There is some evidence that use of HRT patches (as opposed to pills) may not increase stroke risk, but this needs to be confirmed (Henderson and Lobo).
  • 13. Recent Debates: HRT and bone HRT and bone Taking HRT confers some benefit to bone strength (Farquhar C et al, Cochrane Database Syst Rev. 2009 Apr 15;(2):CD004143) Fractures The WHI "Global Index", which looked at the balance of risks and benefits, inappropriately downgraded the importance of fractures. HRT gives more bone benefits than many other drugs (e.g. bisphosphonates), and so restrictions on HRT use as a first-line therapy are not appropriate (de Villiers and Stevenson)
  • 14. HRT and UG + sexual health HRT and UG + sexual health Around 50% of postmenopausal women will suffer urogenital atrophy. Studies indicate that locally applied hormone therapy is generally more effective than systemic HRT for urogenital symptoms, including dyspareunia, which can be a critical determinant of a woman’s interest in sex.(Nappi & Davis) E-P is effective for relief of lower urinary tract symptoms related to estrogen deficiency Most studies show that in post menopausal women with urinary incontinence, E-alone and E-P are not beneficial and may worsen the condition
  • 15. Recent Debates: HRT and QoL HRT and QoL WHI - HRT use led to minimal improvement in quality of life WHI study wasn’t designed to look at wemen going through the menopause - underestimated the real extent of effect of HRT on QoL - hence suffering to many women Some studies indicate that E-P improves many domain of QoL - mental health and depressive symptoms, physical functioning, bodily pain and sleep.
  • 16. Recent Debates: HRT and dementia HRT and dementia Initial WHI results showed an increase in dementia for both E+P and E alone users. ? may be influenced by the timing of the HRT initiation, with benefits for those starting nearer the menopause, but increased risks for women starting at older ages (Maki and Henderson).
  • 17. Current recommendations The risks associated with the use of HRT are low and duration of use may, if necessary, be extended, as the use of HRT for many women provides welcome relief from distressing postmenopausal symptoms (Grady & Barrett-Connor, BMJ 2007; 334:860-1). Start early, use the lowest dose which gives symptom control, for the shortest period of time (Benefit outweighs the risks) ‘window-of-opportunity' - before the age of 60 and/or within 10 years of the menopause. This reduces the risk of coronary heart disease and overall mortality. HRT is more effective for this than other medicines such as statins and aspirin, and is cost-effective. Starting HRT later than this increases risks to women (Hodis et al). All women commencing HRT should be advised of type, dose, mode of delivery and duration Tailor treatment to individual patients
  • 18. References Effect of Hormone Therapy on Risk of Heart Disease May Vary by Age and Years Since Menopause. Additional analyses from the Women’s Health Initiative. NHI News April 2007 The Women’s Health Initiative study and Hormone Therapy – what have we learned 10 years on? International Menopause Society. May 2012 Wallace, Robert. The Women’s Health Initiative: The Role of Hormonal Therapy in Disease Prevention Women’s Health Initiative. http://www.nhlbi.nih.gov/whi/ Hormone Therapy During Menopause in Malaysian Women. Clinical Practice Guidelines July 2010.