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西那卡塞用于肾移植后持续性继发性甲状旁腺功能亢进的初步经验。

Preliminary experience with cinacalcet use in persistent secondary hyperparathyroidism after kidney transplantation.

作者信息

El-Amm Jose-Marie, Doshi Mona D, Singh Atul, Migdal Stephen, Morawski Katherina, Sternbauer Diane, Cincotta Elizabeth, West Miguel S, Losanoff Julian E, Gruber Scott A

机构信息

Division of Nephrology, Department of Medicine, Wayne State University School of Medicine, Harper Professional Building, Detroit, MI 48201, USA.

出版信息

Transplantation. 2007 Mar 15;83(5):546-9. doi: 10.1097/01.tp.0000253429.33198.2f.

Abstract

BACKGROUND

There is limited experience with the use of cinacalcet in the treatment of persistent secondary hyperparathyroidism after kidney transplantation.

METHODS

We retrospectively analyzed our experience in 18 renal allograft recipients who initiated cinacalcet therapy from 1 month to 23 years (median 3 years) posttransplantation and were maintained on the drug for 6 months. The daily dose was titrated from 30 mg up to a maximum of 180 mg to achieve a reduction in serum intact parathyroid hormone (PTH) levels.

RESULTS

Sustainable, significant decreases in mean calcium and alkaline phosphatase were noted at 1 month and intact PTH by 3 months, with 50% of patients achieving at least a 30% drop in PTH levels at 6 months. Serum phosphorous increased at 6 months, whereas urine N-telopeptides decreased. There were no significant changes in serum osteocalcin, albumin, and hemoglobin levels. We did not observe a tachyphylaxis phenomenon. Two patients reported occasional nausea, but did not require medication discontinuation. Estimated glomerular filtration rate did decrease progressively over the 6-month period.

CONCLUSION

Cinacalcet appears to be an effective drug for the treatment of posttransplant hypercalcemia due to persistent secondary hyperparathyroidism. Further studies with more patients and longer follow-up will be needed to better elucidate the efficacy/safety profile for this agent, particularly with regard to long-term bone histology and renal outcomes.

摘要

背景

在肾移植后持续性继发性甲状旁腺功能亢进的治疗中,使用西那卡塞的经验有限。

方法

我们回顾性分析了18例肾移植受者的经验,这些患者在移植后1个月至23年(中位时间3年)开始使用西那卡塞治疗,并持续用药6个月。每日剂量从30毫克滴定至最大180毫克,以降低血清完整甲状旁腺激素(PTH)水平。

结果

1个月时平均钙和碱性磷酸酶持续显著下降,3个月时完整PTH下降,6个月时50%的患者PTH水平至少下降30%。6个月时血清磷升高,而尿N-端肽下降。血清骨钙素、白蛋白和血红蛋白水平无显著变化。我们未观察到快速耐受现象。两名患者报告偶尔有恶心,但无需停药。估计肾小球滤过率在6个月期间确实逐渐下降。

结论

西那卡塞似乎是治疗因持续性继发性甲状旁腺功能亢进导致的移植后高钙血症的有效药物。需要更多患者和更长随访时间的进一步研究,以更好地阐明该药物的疗效/安全性,特别是在长期骨组织学和肾脏结局方面。

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