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骨转换生化标志物和骨密度在骨质疏松症管理中的效用。

Utility of biochemical markers of bone turnover and bone mineral density in management of osteoporosis.

作者信息

Vasikaran Samuel D

机构信息

Department of Core Clinical Pathology and Biochemistry, PathWest Laboratory Medicine, Royal Perth Hospital, Perth, WA, Australia.

出版信息

Crit Rev Clin Lab Sci. 2008;45(2):221-58. doi: 10.1080/10408360801949442.

Abstract

Biochemical markers of bone turnover (bone-turnover markers) are released during bone formation or resorption and can be measured in blood and/or urine. The concentration of bone-turnover markers in serum or urine reflect bone remodeling activity and can potentially be used as surrogate markers of the rate of bone formation or bone resorption. While the diagnosis of osteoporosis is based on bone mineral density (BMD), the absolute fracture risk for a particular BMD measurement varies several fold depending on age and is also influenced by other clinical risk factors. The measurement of bone-turnover markers may be of additional value to BMD and clinical risk factors in fracture risk assessment by improving the sensitivity and specificity of prediction of future fractures. In clinical practice, bone-turnover markers may help make cost-effective treatment decisions in patients with borderline absolute risk. BMD changes following treatment cannot be detected with confidence for 12-24 months due to measurement imprecision. Bone-turnover markers, which show an early response following treatment, may be useful for monitoring therapy, identifying non-compliance and non-responders, and predicting early response to therapy. This review concludes by identifying the need for internationally agreed-upon standards for bone resorption and formation.

摘要

骨转换生化标志物(骨转换标志物)在骨形成或骨吸收过程中释放,可在血液和/或尿液中进行检测。血清或尿液中骨转换标志物的浓度反映骨重塑活性,并有可能用作骨形成或骨吸收速率的替代标志物。虽然骨质疏松症的诊断基于骨密度(BMD),但特定骨密度测量的绝对骨折风险因年龄而异,相差数倍,且还受其他临床风险因素的影响。在骨折风险评估中,通过提高预测未来骨折的敏感性和特异性,骨转换标志物的检测对于骨密度和临床风险因素可能具有额外价值。在临床实践中,骨转换标志物可能有助于为绝对风险处于临界值的患者做出具有成本效益的治疗决策。由于测量不精确,治疗后12 - 24个月内无法可靠地检测到骨密度变化。骨转换标志物在治疗后显示出早期反应,可能有助于监测治疗、识别不依从和无反应者,以及预测对治疗的早期反应。本综述最后指出需要制定国际公认的骨吸收和形成标准。

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