Osteoporosis diagnosis and screening

Clinical cornerstone Pub Date : 2006-01-01 Epub Date: 2007-06-22 DOI:10.1016/S1098-3597(06)80061-X
MD Andrea Singer (Associate Professor)
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引用次数: 30

Abstract

Osteoporosis and osteoporotic fracture are major causes of morbidity and mortality in the United States and worldwide. Nearly half of all women and one quarter of men >50 years of age will experience an osteoporosis-related fracture during their lifetime. The diagnosis of osteoporosis in postmenopausal women and older men can be made definitively by comparing bone mineral density (BMD) measurements from dual-energy x-ray absorptiometry (DXA) to mean peak bone mass in young adults. Efforts to increase access to DXA and improve the sensitivity and specificity of osteoporosis risk assessment instruments may help ensure that individuals with osteoporosis are diagnosed early. The early identification of individuals with low BMD and/or clinical risk factors, accurate diagnosis of osteoporosis and osteopenia, and initiation of appropriate treatment are crucial to reducing the incidence of vertebral and nonvertebral fractures. The World Health Organization is moving toward absolute risk assessment and this may help to better identify patients for screening and treatment in the future.

骨质疏松症的诊断和筛查
骨质疏松症和骨质疏松性骨折是美国和全世界发病率和死亡率的主要原因。近一半的女性和四分之一的50岁男性在他们的一生中会经历骨质疏松相关的骨折。绝经后女性和老年男性骨质疏松症的诊断可以通过比较双能x线骨密度(DXA)测量的骨密度(BMD)和年轻成人的平均峰值骨量来确定。努力增加获得DXA的机会,提高骨质疏松症风险评估工具的敏感性和特异性,可能有助于确保骨质疏松症患者得到早期诊断。早期识别低骨密度和/或临床危险因素,准确诊断骨质疏松症和骨质减少症,并开始适当的治疗对于减少椎体和非椎体骨折的发生率至关重要。世界卫生组织正朝着绝对风险评估的方向发展,这可能有助于更好地确定患者,以便在未来进行筛查和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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