Hormone Therapy for the Prevention of Bone Loss in Menopausal Women with OsteopeniaIs it a Viable Option?

被引:0
作者
Mary H. Hohenhaus
Kelly A. McGarry
Nananda F. Col
机构
[1] Brown University,Department of Medicine
[2] The Miriam Hospital,Department of Medicine
[3] Brown University,undefined
[4] Rhode Island Hospital,undefined
[5] Center for Outcomes Research and Evaluation,undefined
[6] Maine Medical Center,undefined
来源
Drugs | 2007年 / 67卷
关键词
Bone Mineral Density; Osteoporosis; Hormone Therapy; Vertebral Fracture; Fracture Risk;
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摘要
Osteopenia is a state of low bone mass, the appropriate clinical management of which is not always clear. The use of hormone therapy for postmenopausal bone loss has become controversial given recent data regarding the risks of therapy. Fragility fractures are common, and result in substantial morbidity and mortality. Although the fracture rate is higher among osteoporotic women, the substantially larger population of osteopenic women accounts for a higher absolute number of fractures. Osteopenia is defined solely according to the statistical properties of the distribution of bone mineral density (BMD) values, which limits its usefulness in clinical care. BMD, although inversely related to fracture risk, should not be used as the sole criterion for fracture risk. Limited data suggest that benefits of treatment seen in women with documented osteoporosis may not extend to osteopenic women. Although estrogen prevents postmenopausal bone loss, preservation of BMD does not necessarily translate into reduced fracture risk. In making decisions about whether to treat a woman with osteopenia, it is critical to estimate how treatments will affect the individual’s risk of fracture. Treatment decisions should be based on whether the net benefits of treatment outweigh the anticipated risks, which will depend on the age of the patient and her risk profile. In our opinion, there is insufficient evidence to support treatment for women with a BMD in the osteopenic range in the absence of fragility fracture. For osteopenic women with higher risk, the availability of other treatments with a more favourable risk-benefit profile eliminates the role of hormone therapy for fracture prevention.
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页码:2311 / 2321
页数:10
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