New Mexico Clinical Research & Osteoporosis Center, 300 Oak St. NE, Albuquerque, NM 87106, USA.
Rev Endocr Metab Disord. 2010 Dec;11(4):261-73. doi: 10.1007/s11154-010-9126-4.
Osteoporosis is a common disease characterized by low bone strength that increases the risk of fractures. The consequences of fractures include increases in morbidity, mortality, and healthcare costs. Randomized clinical trials have shown that pharmacological therapy can reduce the risk of fractures. In clinical practice, however, failure to achieve optimal therapeutic benefit is common for reasons that include taking medication incorrectly, stopping it prematurely, malabsorption, and the presence of unrecognized diseases or conditions with adverse skeletal effects. Monitoring for anti-fracture effectiveness in individual patients is limited by the absence of clinical tools to directly measure bone strength. It is therefore necessary to monitor therapy with biomarkers such as bone mineral density and bone turnover markers. This is a review of the utility of these tools in the care of individual patients.
骨质疏松症是一种常见的疾病,其特征是骨强度低,增加骨折的风险。骨折的后果包括发病率、死亡率和医疗保健成本的增加。随机临床试验表明,药物治疗可以降低骨折的风险。然而,在临床实践中,由于药物使用不正确、过早停药、吸收不良以及存在未被识别的具有骨骼不良影响的疾病或情况等原因,常常无法达到最佳治疗效果。由于缺乏直接测量骨强度的临床工具,因此对个体患者的抗骨折效果进行监测是有限的。因此,有必要使用骨密度和骨转换标志物等生物标志物来监测治疗。这是对这些工具在个体患者护理中的应用的综述。