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西那卡塞治疗遗传性维生素D抵抗性佝偻病的经验

Cinacalcet treatment experience in hereditary vitamin D resistant rickets.

作者信息

Lucas Jesús, Badia Jose Luis, Lucas Elena, Remon Ana

机构信息

Pediatric Nephrology, General University Hospital of Castellón, Castellón, Spain.

Hospital of Manises, Manises, Spain.

出版信息

J Pediatr Endocrinol Metab. 2020 Feb 25;33(2):313-318. doi: 10.1515/jpem-2019-0258.

Abstract

Background Hereditary vitamin D resistant rickets (HVDRR) is a bone disorder characterized by a phenotype of rickets with onset at early stage of life with elevated alkaline phosphatase, hypocalcemia, hypophosphatemia, hyperparathyroidism and elevated levels of 1,25-dihydroxyvitamin D (calcitriol) as a consequence of the resistance of the vitamin D receptor (VDR). Mutations in the DNA-binding domain of the VDR of the vitamin D receptor have been characterized by a lack of response to traditional treatment with calcium and calcitriol. Secondary hyperparathyroidism and hypophosphatemia are the main factors in its pathogenesis. Cinacalcet is a calciomimetic drug that reproduces the action of calcium by increasing the sensitivity of the calcium-sensitive receptors (CASR) of the parathyroid glands that regulate the secretion of the parathyroid hormone (PTH). Case presentation We describe its effectiveness and safety in a patient with HVDRR and review other published report cases in the literature. According to published experience, cinacalcet could be used as an adjunctive treatment for the HVDRR with mutations in the DNA-binding domain of the VDR refractory to traditional treatment. Due to lack of knowledge of possible effects of cinacalcet on CASR in the skeleton, long-term use should be avoided. Conclusions The optimal dose of cinacalcet for treatment of HVDRR ranges between 0.25 and 0.5 mg/kg/day. Serious side effects of cinacalcet have not been published in this type of patient, although we considered that a close monitoring is necessary in order to detect hypocalcemia.

摘要

背景 遗传性维生素D抵抗性佝偻病(HVDRR)是一种骨骼疾病,其特征为佝偻病表型,在生命早期发病,伴有碱性磷酸酶升高、低钙血症、低磷血症、甲状旁腺功能亢进以及由于维生素D受体(VDR)抵抗导致的1,25 - 二羟维生素D(骨化三醇)水平升高。维生素D受体的VDR DNA结合域中的突变表现为对传统的钙和骨化三醇治疗无反应。继发性甲状旁腺功能亢进和低磷血症是其发病机制的主要因素。西那卡塞是一种拟钙剂药物,通过增加调节甲状旁腺激素(PTH)分泌的甲状旁腺钙敏感受体(CASR)的敏感性来模拟钙的作用。病例报告 我们描述了其在一名HVDRR患者中的有效性和安全性,并回顾了文献中其他已发表的报告病例。根据已发表的经验,西那卡塞可作为对传统治疗难治的VDR DNA结合域突变的HVDRR的辅助治疗。由于缺乏关于西那卡塞对骨骼中CASR可能影响的知识,应避免长期使用。结论 治疗HVDRR的西那卡塞最佳剂量范围为0.25至0.5毫克/千克/天。尽管我们认为需要密切监测以检测低钙血症,但西那卡塞在这类患者中的严重副作用尚未见报道。

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