Morris H A, Eastell R, Jorgensen N R, Cavalier E, Vasikaran S, Chubb S A P, Kanis J A, Cooper C, Makris K
School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA 5000, Australia.
Mellanby Centre for Bone Research, University of Sheffield and Metabolic Bone Centre, Northern General Hospital, Herries Road, Sheffield, UK.
Clin Chim Acta. 2017 Apr;467:34-41. doi: 10.1016/j.cca.2016.06.036. Epub 2016 Jun 30.
Current evidence continues to support the potential for bone turnover markers (BTM) to provide clinically useful information particularly for monitoring the efficacy of osteoporosis treatment. Many of the limitations identified earlier remain, principally in regard to the relationship between BTM and incident fractures. Important data are now available on reference interval values for CTX and PINP across a range of geographic regions and for individual clinical assays. An apparent lack of comparability between current clinical assays for CTX has become evident indicating the possible limitations of combining such data for meta-analyses. Harmonization of units for reporting serum/plasma CTX (ng/L) and PINP (μg/L) is recommended. The development of international collaborations continues with an important initiative to combine BTM results from clinical trials in osteoporosis in a meta-analysis and an assay harmonization program are likely to be beneficial. It is possible that knowledge derived from clinical studies can further enhance fracture risk estimation tools with inclusion of BTM together with other independent risk factors. Further data of the relationships between the clinical assays for CTX and PINP as well as physiological and pre-analytical factors contributing to variability in BTM concentrations are required.
现有证据继续支持骨转换标志物(BTM)提供临床有用信息的潜力,特别是在监测骨质疏松症治疗效果方面。早期发现的许多局限性仍然存在,主要涉及BTM与新发骨折之间的关系。现在已有关于不同地理区域以及个体临床检测中CTX和PINP参考区间值的重要数据。目前CTX临床检测之间明显缺乏可比性,这表明将此类数据用于荟萃分析可能存在局限性。建议统一血清/血浆CTX(ng/L)和PINP(μg/L)的报告单位。国际合作仍在继续,一项重要举措是将骨质疏松症临床试验中的BTM结果纳入荟萃分析,检测方法协调计划可能会有所帮助。临床研究得出的知识有可能通过将BTM与其他独立风险因素一起纳入,进一步改进骨折风险评估工具。还需要有关CTX和PINP临床检测之间的关系以及导致BTM浓度变化的生理和分析前因素的更多数据。