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骨质疏松症患者甲状旁腺素治疗期间的低镁血症:发生率及决定因素。

Hypomagnesemia During Teriparatide Treatment in Osteoporosis: Incidence and Determinants.

机构信息

Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

Endocrinology Division, Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

出版信息

J Bone Miner Res. 2018 Aug;33(8):1444-1449. doi: 10.1002/jbmr.3438. Epub 2018 May 17.

Abstract

In our clinical experience, we have encountered patients who developed hypomagnesemia after the introduction of teriparatide. Some trials have reported hypomagnesemia as an adverse event during teriparatide treatment, but this issue had never been studied specifically. Our objective was twofold: 1) determine the incidence of hypomagnesemia (serum magnesium <0.7 mmol/L) associated with teriparatide in a retrospective cohort and 2) identify the predisposing factors to hypomagnesemia in this cohort. We reviewed the files of 53 patients treated for severe osteoporosis with teriparatide for 6 to 24 months between May 2008 and January 2016. Serum magnesium levels were measured at 0, 3, 6, 12, 18, and 24 months. In the full cohort, we observed an average decrease of serum magnesium of 0.075 mmol/L, 0.069 mmol/L, 0.085 mmol/L, 0.086 mmol/L (p < 0.001) at 3, 6, 12 months, and at the end of the treatment, respectively. The cumulative incidence of hypomagnesemia during treatment with teriparatide was 35.9% (19 patients). Patients' older age (71.1 versus 65.1 years; p = 0.05) and lower baseline level of magnesium before teriparatide treatment (0.81 mmol/L versus 0.85 mmol/L; p = 0.03) were significant risk factors for teriparatide-induced hypomagnesemia. The average decrease of serum magnesium was greater in the patients who developed hypomagnesemia compared with normomagnesemic patients at 3 months (0.110 mmol/L versus 0.054 mmol/L; p = 0.02), 6 months (0.139 mmol/L versus 0.036 mmol/L; p < 0.001), and 12 months (0.156 mmol/L versus 0.048 mmol/L; p < 0.001). Serum calcium, creatinine, and parathyroid hormone remained normal throughout the treatment period. We observed a statistically significant decrease in the serum magnesium levels in patients treated with teriparatide for severe osteoporosis. Older age and lower baseline magnesium were significant determinants of hypomagnesemia. Closer monitoring of serum magnesium level should be considered in these patients. © 2018 American Society for Bone and Mineral Research.

摘要

在我们的临床经验中,我们遇到了一些在使用特立帕肽后出现低镁血症的患者。一些试验报告了特立帕肽治疗期间低镁血症作为一种不良反应,但这个问题从未被专门研究过。我们的目的有两个:1)确定在回顾性队列中特立帕肽治疗相关的低镁血症(血清镁<0.7mmol/L)的发生率;2)确定该队列中低镁血症的易患因素。我们回顾了 2008 年 5 月至 2016 年 1 月期间,53 名患有严重骨质疏松症的患者接受特立帕肽治疗 6 至 24 个月的档案。在 0、3、6、12、18 和 24 个月时测量血清镁水平。在整个队列中,我们观察到血清镁分别在 3、6、12 个月和治疗结束时平均下降了 0.075mmol/L、0.069mmol/L、0.085mmol/L、0.086mmol/L(p<0.001)。特立帕肽治疗期间低镁血症的累积发生率为 35.9%(19 例)。患者年龄较大(71.1 岁比 65.1 岁;p=0.05)和特立帕肽治疗前较低的基线镁水平(0.81mmol/L 比 0.85mmol/L;p=0.03)是特立帕肽引起低镁血症的显著危险因素。与正常镁血症患者相比,发生低镁血症的患者在 3 个月(0.110mmol/L 比 0.054mmol/L;p=0.02)、6 个月(0.139mmol/L 比 0.036mmol/L;p<0.001)和 12 个月(0.156mmol/L 比 0.048mmol/L;p<0.001)时的血清镁平均下降幅度更大。整个治疗期间血清钙、肌酐和甲状旁腺激素均保持正常。我们观察到严重骨质疏松症患者接受特立帕肽治疗后血清镁水平有统计学意义的下降。年龄较大和较低的基线镁水平是低镁血症的显著决定因素。这些患者应考虑更密切监测血清镁水平。©2018 美国骨矿研究协会。

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