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骨折后骨质疏松症治疗监测中骨转换标志物的目标值及日间变化

Target Values and Daytime Variation of Bone Turnover Markers in Monitoring Osteoporosis Treatment After Fractures.

作者信息

Borgen Tove T, Solberg Lene B, Lauritzen Trine, Apalset Ellen M, Bjørnerem Åshild, Eriksen Erik F

机构信息

Department of Rheumatology Vestre Viken Hospital Trust, Drammen Hospital Drammen Norway.

Division of Orthopedic Surgery Oslo University Hospital Oslo Norway.

出版信息

JBMR Plus. 2022 May 9;6(6):e10633. doi: 10.1002/jbm4.10633. eCollection 2022 Jun.

Abstract

The serum bone turnover markers (BTM) procollagen type 1 N-terminal propeptide (P1NP) and C-terminal cross-linking telopeptide of type 1 collagen (CTX) are recommended for monitoring adherence and response of antiresorptive drugs (ARD). BTM are elevated about 1 year after fracture and therefore BTM target values are most convenient in ARD treatment follow-up of fracture patients. In this prospective cohort study, we explored the cut-off values of P1NP and CTX showing the best discriminating ability with respect to adherence and treatment effects, reflected in bone mineral density (BMD) changes. Furthermore, we explored the ability of BTM to predict subsequent fractures and BTM variation during daytime in patients using ARD or not. After a fragility fracture, 228 consenting patients (82.2% women) were evaluated for ARD indication and followed for a mean of 4.6 years (SD 0.5 years). BMD was measured at baseline and after 2 years. Serum BTM were measured after 1 or 2 years. The largest area under the curve (AUC) for discrimination of patients taking ARD or not was shown for P1NP <30 μg/L and CTX <0.25 μg/L. AUC for discrimination of patients with >2% gain in BMD (lumbar spine and total hip) was largest at cut-off values for P1NP <30 μg/L and CTX <0.25 μg/L. Higher P1NP was associated with increased fracture risk in patients using ARD (hazard ratio [HR] = 15.0; 95% confidence interval [CI] 2.7-83.3),  = 0.002. P1NP and CTX were stable during daytime, except in those patients not taking ARD, where CTX decreased by 21% per hour during daytime. In conclusion, P1NP <30 μg/L and CTX <0.25 μg/L yield the best discrimination between patients taking and not taking ARD and the best prediction of BMD gains after 2 years. Furthermore, higher P1NP is associated with increased fracture risk in patients on ARD. BTM can be measured at any time during the day in patients on ARD. © 2022 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.

摘要

血清骨转换标志物(BTM)1型前胶原N端前肽(P1NP)和1型胶原C端交联末肽(CTX)被推荐用于监测抗吸收药物(ARD)的依从性和反应。骨折后约1年BTM会升高,因此在骨折患者的ARD治疗随访中,BTM目标值最为方便。在这项前瞻性队列研究中,我们探讨了P1NP和CTX的截断值,这些截断值在反映骨密度(BMD)变化的依从性和治疗效果方面具有最佳的区分能力。此外,我们还探讨了BTM预测后续骨折的能力以及使用或未使用ARD的患者白天BTM的变化情况。在发生脆性骨折后,对228名同意参与的患者(82.2%为女性)进行了ARD指征评估,并平均随访4.6年(标准差0.5年)。在基线和2年后测量BMD。在1年或2年后测量血清BTM。对于区分服用或未服用ARD的患者,P1NP<30μg/L和CTX<0.25μg/L的曲线下面积(AUC)最大。对于区分BMD(腰椎和全髋)增加>2%的患者,P1NP<30μg/L和CTX<0.25μg/L的截断值时AUC最大。在使用ARD的患者中,较高的P1NP与骨折风险增加相关(风险比[HR]=15.0;95%置信区间[CI]2.7-83.3),P=0.002。除了未服用ARD的患者外,P1NP和CTX在白天是稳定的,在未服用ARD的患者中,CTX在白天每小时下降21%。总之,P1NP<30μg/L和CTX<0.25μg/L在区分服用和未服用ARD的患者方面效果最佳,并且对2年后的BMD增加预测效果最佳。此外,在使用ARD的患者中,较高的P1NP与骨折风险增加相关。对于使用ARD的患者,可以在一天中的任何时间测量BTM。©2022作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9906/9189911/a6ff217a1072/JBM4-6-e10633-g003.jpg

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