Kim Beom Jun, Lee Seung Hun, Koh Jung Min
Division of Endocrinology and Metabolism, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Endocrinol Metab (Seoul). 2020 Mar;35(1):55-63. doi: 10.3803/EnM.2020.35.1.55.
Osteoporotic fracture (OF) is associated with high disability and morbidity rates. The burden of OF may be reduced by early identification of subjects who are vulnerable to fracture. Although the current fracture risk assessment model includes clinical risk factors (CRFs) and bone mineral density (BMD), its overall ability to identify individuals at high risk for fracture remains suboptimal. Efforts have therefore been made to identify potential biomarkers that can predict the risk of OF, independent of or combined with CRFs and BMD. This review highlights the emerging biomarkers of bone metabolism, including sphongosine-1-phosphate, leucine-rich repeat-containing 17, macrophage migration inhibitory factor, sclerostin, receptor activator of nuclear factor-κB ligand, and periostin, and the importance of biomarker risk score, generated by combining these markers, in enhancing the accuracy of fracture prediction.
骨质疏松性骨折(OF)与高致残率和高发病率相关。通过早期识别易发生骨折的个体,OF的负担可能会减轻。尽管当前的骨折风险评估模型包括临床风险因素(CRF)和骨密度(BMD),但其识别骨折高危个体的整体能力仍不理想。因此,人们一直在努力寻找能够独立于CRF和BMD或与之结合来预测OF风险的潜在生物标志物。本综述重点介绍了骨代谢领域新出现的生物标志物,包括1-磷酸鞘氨醇、富含亮氨酸重复序列17、巨噬细胞迁移抑制因子、硬化蛋白、核因子κB受体激活剂配体和成骨素,以及通过组合这些标志物生成的生物标志物风险评分在提高骨折预测准确性方面的重要性。