Department of Orthopaedic Surgery, Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
J Bone Joint Surg Am. 2010 Mar;92(3):743-53. doi: 10.2106/JBJS.I.00919.
Bone mineral density is considered to be the standard measure for the diagnosis of osteoporosis and the assessment of fracture risk. The majority of fragility fractures occur in patients with bone mineral density in the osteopenic range. The Fracture Risk Assessment Tool (FRAX) can be used as an assessment modality for the prediction of fractures on the basis of clinical risk factors, with or without the use of femoral neck bone mineral density. Treatment of osteoporosis should be considered for patients with low bone mineral density (a T-score of between -1.0 and -2.5) as well as a ten-year risk of hip fracture of > or = 3% or a ten-year risk of a major osteoporosis-related fracture of > or = 20% as assessed with the FRAX. Biochemical bone markers are useful for monitoring the efficacy of antiresorptive or anabolic therapy and may aid in identifying patients who have a high risk of fracture. An approach combining the assessment of bone mineral density, clinical risk factors for fracture with use of the FRAX, and bone turnover markers will improve the prediction of fracture risk and enhance the evaluation of patients with osteoporosis.
骨密度被认为是骨质疏松症诊断和骨折风险评估的标准方法。大多数脆性骨折发生在骨密度处于骨质疏松范围内的患者中。骨折风险评估工具(FRAX)可作为基于临床危险因素的骨折预测评估方式,无论是否使用股骨颈骨密度。对于骨密度低(T 评分在-1.0 到-2.5 之间)的患者,以及使用 FRAX 评估髋部骨折 10 年风险大于或等于 3%或主要骨质疏松性骨折 10 年风险大于或等于 20%的患者,应考虑骨质疏松症的治疗。生化骨标志物可用于监测抗吸收或合成代谢治疗的疗效,并有助于识别骨折风险高的患者。结合骨密度评估、骨折临床危险因素和骨转换标志物的方法将提高骨折风险预测能力,并增强对骨质疏松症患者的评估。