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接受双膦酸盐治疗的颌骨骨坏死患者的前瞻性生物标志物评估。

Prospective biomarker evaluation in patients with osteonecrosis of the jaw who received bisphosphonates.

机构信息

Department of Oral and Maxillofacial Surgery, Ewha Womans University, Seoul, Republic of Korea.

出版信息

Bone. 2013 Nov;57(1):201-5. doi: 10.1016/j.bone.2013.08.005. Epub 2013 Aug 14.

Abstract

Bone biomarkers have been suggested for the risk assessment for osteonecrosis of the jaw, a serious complication associated with bisphosphonate (BP) use; however, no consensus has been reached. This study investigated the possible associations between bone biomarkers and the development of bisphosphonates-related osteonecrosis of the jaw (BRONJ). This is a case-control study of 37 patients with BRONJ (age, 73.6±11.2years) who had at least 1 sample available at diagnosis, out of which, 35 were taking BPs for osteoporosis and 2 patients for bone metastasis. Age- and gender-matched 37 patients who had been exposed to BPs for >24months and had no evidence of BRONJ after dentoalveolar surgery served as control group. The association between biomarkers (osteocalcin [OC], deoxypyridinoline [DPD], C-terminal telopeptide of collagen I [CTX], N-terminal telopeptides [NTX], bone-specific alkaline phosphatase [BAP], and parathyroid hormone [PTH]) and BRONJ development, the effects of BP discontinuation on biomarkers, and the performance of biomarkers for risk assessment were investigated. In our study, the PTH levels were found to be significantly higher in BRONJ patients compared to controls (P<0.05). But the OC, DPD, CTX, NTX, and BAP levels were not significantly different between the 2 groups (P>0.05). The CTX level in reference to a 150pg/mL cutoff was also not significant for BRONJ development (P>0.05). Among BRONJ patients who discontinued BP, in a linear mixed model, only CTX showed a significant increase over time (β=0.002, P=0.007). The cutoff PTH level was >41.52pg/mL (AUC=0.719, P=0.009), and that of CTX was ≤0.094ng/mL (AUC=0.619, P=0.069). In conclusion, there is insufficient evidence for the risk prediction for BRONJ of current bone biomarkers; additional research is necessary.

摘要

骨生物标志物已被提议用于评估颌骨骨坏死(BRONJ)的风险,这是一种与双膦酸盐(BP)使用相关的严重并发症;然而,目前尚未达成共识。本研究探讨了骨生物标志物与双膦酸盐相关颌骨骨坏死(BRONJ)之间可能存在的关联。这是一项病例对照研究,共纳入 37 名 BRONJ 患者(年龄 73.6±11.2 岁),其中至少有 1 个样本在诊断时可用,其中 35 名患者因骨质疏松症接受 BP 治疗,2 名患者因骨转移接受 BP 治疗。年龄和性别匹配的 37 名患者在接受 BP 治疗>24 个月后,经牙槽外科手术后无 BRONJ 证据,作为对照组。研究了生物标志物(骨钙素 [OC]、脱氧吡啶啉 [DPD]、I 型胶原 C 末端肽 [CTX]、N 末端肽 [NTX]、碱性磷酸酶 [BAP]和甲状旁腺激素 [PTH])与 BRONJ 发展之间的关联、BP 停药对生物标志物的影响以及生物标志物进行风险评估的性能。在我们的研究中,与对照组相比,BRONJ 患者的 PTH 水平显著升高(P<0.05)。但 2 组之间 OC、DPD、CTX、NTX 和 BAP 水平无显著差异(P>0.05)。CTX 水平与 150pg/mL 临界值相比对 BRONJ 发展也无显著性差异(P>0.05)。在停止 BP 治疗的 BRONJ 患者中,在线性混合模型中,只有 CTX 随时间呈显著增加(β=0.002,P=0.007)。PTH 水平的截断值>41.52pg/mL(AUC=0.719,P=0.009),CTX 水平的截断值≤0.094ng/mL(AUC=0.619,P=0.069)。总之,目前尚无足够的证据表明当前骨生物标志物可用于预测 BRONJ 风险;需要进一步研究。

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