A 68-year-old postmenopausal woman presents in her family physician’s office to discuss the results of her recent bone mineral density test. She has a T-score of −2.2 at the femoral neck and 1.9 at the lumbar spine. She has no history of fracture and is otherwise healthy. She wonders if her low bone density requires treatment.
What is the 10-year risk of fracture?
There are two models available in Canada to assess risk of fracture: the Fracture Risk Assessment Tool (FRAX; available at www.shef.ac.uk/FRAX) and the Canadian Association of Radiologists and Osteoporosis Canada tool (available at www.osteoporosis.ca).1 Recent guidelines issued by Osteoporosis Canada state that the choice of tool is a matter of personal preference and convenience.1
The World Health Organization (WHO) launched the FRAX tool in 2008 (Table 1).2 It calculates 10-year probabilities of fracture using multiple global observational databases that integrate clinical risk factors and bone mineral density at the femoral neck. Both the risk of hip fracture and the risk of major osteoporotic fracture are calculated. A FRAX tool calibrated to Canadian rates of hip fracture has been available since July 2010.
Upon questioning, our patient confirmed having a 20 pack-year history of smoking with no intention of quitting and that she drinks less than two units of alcohol per day. There is no family history of osteoporosis or fractures. The patient’s menopause occurred at 50 years of age, for which she did not receive hormone therapy. The patient has never taken glucocorticoids and has no other medical conditions, but she reports a 3-inch loss of height over her lifetime. The patient takes 1200 mg of elemental calcium from diet and supplements, as well as 400 IU vitamin D daily. She walks for 30 minutes each day. On examination, the patient weighs 70 kg, with a height of 165 cm and a body mass index of 25.7 kg/m2. A spinal examination shows that the patient has an upright posture with no kyphotic deformity. The patient’s blood pressure is 135/80. The rest of the examination is unremarkable.
Using the patient’s bone mineral density at the femoral neck, the FRAX tool calculates her 10-year probability of major osteoporotic fracture as 12%, with a 3.8% 10-year probability of hip fracture. Using the Canadian Association of Radiologists and Osteoporosis Canada tool, the patient would be considered at moderate risk for fracture (10%–20%).
Is the risk of fracture high enough to warrant medication?
The WHO defines osteoporosis in a postmenopausal woman as a T-score less than or equal to −2.5 at the total hip, femoral neck or lumbar spine.3 The presence of a fragility fracture constitutes a clinical diagnosis of osteoporosis without the need for measuring bone mineral density. By densitometry alone, our patient would have a diagnosis of low bone density (or osteopenia), not osteoporosis.
Guidelines for therapy based on the assessment of 10-year absolute risk of fracture are available for many jurisdictions. The North American Menopause Society and the US National Osteoporosis Foundation recommend that medications be considered for the treatment of osteoporosis in postmenopausal women if any of the following criteria are present:4,5 a fracture of the hip or vertebrae (clinical or morphometric); a T-score of less than −2.5 at the lumbar spine, femoral neck or total hip regions; or a T-score between −1.0 and −2.5 (low bone density) and a 10-year probability of major osteoporotic fracture (spine, hip, proximal humerus and wrist) of at least 20% or a probability of hip fracture of at least 3%, as calculated using the FRAX tool.
Our patient’s 10-year risk of hip fracture using the FRAX calculator is 3.8%, so she exceeds the baseline threshold for pharmacologic treatment as recommended by the North American Menopause Society and the National Osteoporosis Foundation. The patient’s risk of hip fracture increased from 2.2% to 3.8% because of her history of smoking, although this history did not substantially affect her risk of major fracture.
Osteoporosis Canada guidelines do not specify therapy thresholds for 10-year risk of hip fracture and do not include smoking, family history of fracture or consumption of alcohol as risk factors in their evaluation. For patients at moderate risk, as determined using the Canadian Association of Radiologists and Osteoporosis Canada tool, Osteoporosis Canada’s guidelines encourage the consideration of other risk factors in deciding whether medications should be advised. A radiographic image of the patient’s spine showed a 25% wedge compression of the anterior portion of the T12 vertebrae, making her a candidate for pharmacotherapy according to the guidelines of both the North American Menopause Society and Osteoporosis Canada.
Our patient opted to take alendronate. In the Fraction Intervention Trial 2 (FIT-2) of alendronate versus placebo for women with low bone density but no vertebral fracture, alendronate reduced the risk of radiographic vertebral fractures by 44% overall (relative risk, 0.56; 95% confidence interval, 0.39–0.80; treatment–control difference, 1.7%; number needed to treat, 60).6
In the Fracture Intervention Trial (FIT), alendronate was shown to have an absolute risk reduction of 7% (number needed to treat, 14 over 3 yr) and 1.1% (number needed to treat, 91 over 3 yr) for hip fracture in people who had previously had a vertebral fracture.7
What is the recommended daily intake of calcium and vitamin D for this patient?
All postmenopausal women, regardless of their bone density, should be encouraged to get an adequate amount of calcium and vitamin D from their diet and supplements. In women aged 50 years or more, Osteoporosis Canada, the North American Menopause Society and the National Osteoporosis Foundation all recommend a total daily intake of 1200 mg of elemental calcium.1,4,5 A recent meta-analysis suggests a potential increase in the risk of myocardial infarction with high-dose supplementation of calcium.8
A recent Osteoporosis Canada guideline on vitamin D recommends a daily intake of up to 800–2000 IU for women at high risk for osteoporosis or fracture and for older women.1,8 The North American Menopause Society and National Osteoporosis Foundation have suggested that 2000 IU per day is the upper limit of safe intake for vitamin D.1,4,5 Our patient should also be encouraged to quit smoking and to increase her level of physical activity, specifically the amount of weight-bearing exercise she does, such as walking.
What other evaluation is required and what follow-up is advised?
Osteoporosis Canada, among other groups, suggests that patients with low bone density be evaluated for secondary causes of bone loss including renal failure, parathyroid disease, thyroid disease, myeloma and, sometimes, vitamin D deficiency.1 Laboratory investigations before starting treatment may include complete blood count and tests for levels of creatinine, calcium (corrected for albumin), thyroid-stimulating hormone, alkaline phosphatase and 25-hydroxyvitamin D, as well as serum protein electrophoresis and other tests that are clinically indicated.
A follow-up test of a patient’s bone density in one to three years is recommended by Osteoporosis Canada to check for stabilization or increases in bone mineral density.1 Declining bone mineral density (beyond the precision error of the measuring facility) suggests inefficacy of treatment in reducing the risk of fracture. Vitamin D should be measured after three to four months of adequate supplementation in patients with low bone density or osteoporosis and should not be repeated if an optimal level (at least 75 nmol/L) is achieved.1,9
The number needed to treat estimates how many patients in a given risk group will need treatment for a given length of time to prevent one adverse outcome. It is calculated as the inverse of the difference between the proportionate outcomes in the control and treatment groups: 1/[(proportion of outcomes in the control group) – (proportion of outcomes in the treatment group)].
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Footnotes
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Competing interests: David Kendler is a consultant for Amgen, Novartis, Lilly, Pfizer and Merck; he has received grants from Amgen, Novartis, Lilly, Biosante, GlaxoSmithKline and Roche; he has received payment for lectures from Amgen, Lilly, Novartis, Warner Chilcott and Pfizer; and he has been reimbursed for travel expenses by Amgen, Lilly, Novartis, the International Society for Clinical Densitometry and Osteoporosis Canada. No other competing interests were declared.
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This article has been peer reviewed.
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Contributors: Both authors contributed to drafting, revising, and critically reviewing the manuscript and gave their final approval of the version submitted for publication.