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Editorial

A more active role for gynecologists in the prevention of postmenopausal osteoporosis

Pages 293-294 | Published online: 07 Jul 2009

Gynecologists often are the only doctors that postmenopausal women see on a regular basis. This should give an optimal basis for screening for osteoporosis and for the initiation of proper treatment if such a condition has been detected. Unfortunately this may not be the case in routine gynecological practice; only half of the women needing bone density assessment and/or bone medication succeeded to get it during primary care gynecological consultation Citation[1]. Patients themselves may not be aware of the risk of osteoporosis, although they judge a hip fracture as a very serious event and are scared about such a prospect. Instead, apparently healthy postmenopausal women may pay visits to their gynecologists e.g. for the exclusion of gynecological cancer. However, the risk of gynecological cancer amounts only to 3.8% (cervical 0.3%, endometrial 2.3% and ovarian cancer 1.2%) for women between 60 and 85 years of age. In contrast, the risk of future bone fracture in this population is 50%!

Although women may be aware of the importance of lifestyle and dietary factors in bone protection, it makes a big difference if also the gynecologist takes up these issues while seeing postmenopausal women. Regular weight-bearing activity (e.g. 30–60 minutes of walking at least three times a week) strengthens bone. Calcium intake should be of order of 1000–1200 mg/day. Some women ask if excessive calcium is dangerous to blood vessels. We can assure them that the body absorbs only that much calcium needed for bone health; extra calcium passes through the gastrointestinal tract without harming any organ. Vitamin D is needed for calcium (and phosphate) absorption, and that is why each postmenopausal woman should take 800 IU of vitamin D per day through the year. We might add that that besides protecting bone, vitamin D supplementation decreases the risk of colon (and breast?) cancer. Further, we should not forget to mention that smoking is deleterious to bone; and encourage stopping it! These issues, which appear rather simple to busy gynecologists and which therefore may become neglected, should be taken up in each consultation with a postmenopausal woman.

One of the most pertinent questions when meeting postmenopausal women is whose bone mineral density (BMD) should be measured. There are no strict rules on this, but established osteoporosis risk factors (e.g. family history, petite size, heavy smoking, insufficient intake of calcium and/or vitamin D, use of heparin, antiepileptics or thyroxine, history of amenorrhea or premature menopause) should lead to the assessment of BMD. Because the long-term use of hormone therapy (HT) reduces the risk of hip and vertebrae fractures by 30–60%Citation[2],Citation[3], a history of no use of HT should lead to BMD assessment. It is also established that BMD declines by 2.3–6.2% in the first year after stopping HT, and thus BMD in these women should be studied within 3–5 years after the cessation of HT Citation[4]. Some bone societies have recommended that all women from the age of 65 years onwards, or from 60 years if risk factors are present, should be studied at least once for BMD but this decision needs individual clinical judgment. BMD should be assessed in weight-bearing hip and lumbar spine which are most prone to fractures.

Interpretation of BMD scans needs training but each gynecologist can learn it. We must demand good quality control for BMD readings and we can compare two BMD readings only if they are obtained with the same equipment. The impact of low bone density on fracture risk depends on the age of the patient; a femoral neck T-score < −2.5 is associated with hip fracture risk in the next decade in 2.8% if a woman is 50 years old but in 18.3% if she is 70 years old at the time of assessment Citation[5].

The initiation of osteoporosis therapy is indicated if total hip or spine T-score is less than −2.5. The therapy is also indicated if T-score is between −2.0 and −2.5 and there is at least one additional risk factor. Moreover, therapy is always indicated, and even without BMD assessment, if a bone fracture has already occurred Citation[6]. In clinical routine we should avoid the use of unnecessary treatments which just increase costs and which may also cause side-effects, and therefore each treatment decision should carefully considered.

We gynecologists should master all bone treatments. HT is often the most useful regimen for osteopenia and even for mild osteoporosis. The bone maintains its sensitivity towards estrogen up to the senium, and even very low doses (estradiol 0.25 mg orally or 14 μg transdermally) are bone-effective Citation[7-9]. Bisphosphonates (aledronate, risedronate, ibandronate, tsoledronate) all reduce bone resorption, whereas strontium ranelate reduces resorption but may also enhance bone formation. Calcitonin is one option and is especially suitable if vertebral fractures have already occurred because it relieves pains. In our comparative trial on osteoporotic elderly women, HT was at least as effective as alendronate to raise BMD in hip and spine, and a combination of HT and alendronate was not more effective than either agent alone Citation[10]. Thus, in regard to bone, there is no reason to combine HT and bisphosphonate.

To sum up, the large number of post-war ‘baby boomers’ are now slightly above 60 years of age. Due to negative reports in the lay press, the use of bone- protecting HT has been declining. Therefore, osteoporosis is–and will continue to be–a growing dilemma in the Western world. We gynecologists should take a more active role in the screening and treatment of osteoporosis, because we often are the only physicians whom postmenopausal women see on a regular basis.

References

  • Gill J M, Hoffman M K. Prevention and treatment of osteoporosis in primary care offices. Womens Health (Larchmt) 2003; 12: 473–480
  • Cranney A, Guyatt G, Griffith L, Wells G, Tugwell P, Rosen C, Osteoporosis Methodology Group and The Osteoporosis Research Advisory Group. Meta-analyses of therapies for postmenopausal osteoporosis. IX: Summary of meta-analyses of therapies for postmenopausal osteoporosis. Endocr Rev 2002; 23: 570–578
  • Wehren L E, Hosking D, Hochberg M C. Putting evidence-based medicine into clinical practice: comparing anti-resorptive agents for the treatment of osteoporosis. Curr Med Res Opin 2004; 20: 525–531
  • Simon J A, Wehren L E, Ascott-Evans B H, Omizo M K, Silfen S L, Lombardi A. Skeletal consequences of hormone therapy discontinuance: a systematic review. Obstet Gynecol Surv 2006; 61: 115–124
  • Kanis J A, Johnell O, Oden A, De Laet C, de Terlizzi F. Ten-year probabilities of clinical vertebral fractures according to phalangeal quantitative ultrasonography. Osteoporos Int 2005; 16: 1065–1070
  • North American Menopause Society. Management of osteoporosis in postmenopausal women: 2006 position statement of the North American Menopause Society. Menopause 2006; 13: 340–367
  • Prestwood K M, Kenny A M, Kleppinger A, Kulldorff M. Ultralow-dose micronized 17β-estradiol and bone density and bone metabolism in older women: a randomized controlled trial. JAMA 2003; 290: 1042–1048
  • Ettinger B. Rationale for use of lower estrogen doses for postmenopausal hormone therapy. Maturitas 2007; 57: 81–84
  • van de Weijer P H, Matsson L A, Ylikorkala O. Benefits and risks of long-term low-dose oral continuous combined hormone therapy. Maturitas 2007; 56: 231–248
  • Eviö S, Tiitinen A, Laitinen K, Ylikorkala O, Välimäki M J. Effects of alendronate and hormone replacement therapy, alone and in combination, on bone mass and markers of bone turnover in elderly women with osteoporosis. J Clin Endocrinol Metab 2004; 89: 626–631

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