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特立帕肽(重组人甲状旁腺激素)治疗综合征性甲状旁腺功能减退症患儿

Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism.

作者信息

Matarazzo Patrizia, Tuli Gerdi, Fiore Ludovica, Mussa Alessandro, Feyles Francesca, Peiretti Valentina, Lala Roberto

出版信息

J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):53-9. doi: 10.1515/jpem-2013-0159.

Abstract

BACKGROUND

Subcutaneous recombinant human parathormone [rhPTH (1-34)] has been introduced for hypoparathyroidism treatment, allowing avoidance of vitamin D and calcium side effects.

OBJECTIVE

Our objective was to evaluate rhPTH (1-34) safety and efficacy in pediatric patients with genetically proved syndromic hypoparathyroidism.

METHODS

The study was a 2.5-year self-controlled trial on six pediatric patients (four males, two females, age 9.8±5.1 years) with syndromic hypoparathyroidism including three with autoimmune polyendocrinopathy candidiasis ectodermal dysplasia (APECED) syndrome, two with DiGeorge syndrome, and one with hypoparathyroidism-deafness-renal dysplasia syndrome. We compared patients' clinical and biochemical outcome of conventional treatment based on oral administration of calcium (1-1.5 g/day in three doses) plus oral calcitriol (6.5-33 ng/kg per day in two to three doses) with the outcome obtained with rhPTH (1-34) (teriparatide, 12.5 μg bid). Therapy shift was conducted introducing rhPTH (1-34) while progressively withdrawing calcium and vitamin D. Blood calcium, phosphorus, alkaline phosphatase, and urinary calcium-to-creatinine ratio (mg/mg) before and during rhPTH therapy were compared.

RESULTS

rhPTH treatment allowed complete calcium and vitamin D withdrawal in two patients, calcium withdrawal in three and reduction of vitamin D dose in two. During rhPTH (1-34), mean blood calcium, phosphorus, and alkaline phosphatase were not significantly modified, whereas significant reduction of the calciuria-to-creatininuria ratio (0.55±0.31 vs. 0.1±0.1, p=0.02) was obtained. The number of tetanic episodes was reduced in four patients during teriparatide treatment compared to conventional treatment.

CONCLUSION

In children with syndromic hypoparathyroidism, substitutive treatment with rhPTH (1-34) maintains adequate blood calcium levels and allows prompt normalization of urinary calcium excretion, through direct action on the kidney and through calcium and vitamin D therapy layoff.

摘要

背景

皮下注射重组人甲状旁腺激素[rhPTH(1-34)]已被用于治疗甲状旁腺功能减退症,可避免维生素D和钙的副作用。

目的

我们的目的是评估rhPTH(1-34)在经基因证实的综合征性甲状旁腺功能减退症儿科患者中的安全性和疗效。

方法

该研究是一项针对6例综合征性甲状旁腺功能减退症儿科患者(4例男性,2例女性,年龄9.8±5.1岁)的2.5年自我对照试验,其中包括3例自身免疫性多内分泌腺病念珠菌病外胚层发育不良(APECED)综合征患者、2例DiGeorge综合征患者和1例甲状旁腺功能减退症-耳聋-肾发育不良综合征患者。我们将基于口服钙剂(每日1-1.5 g,分3次服用)加口服骨化三醇(每日6.5-33 ng/kg,分2-3次服用)的传统治疗的患者临床和生化结果与rhPTH(1-34)(特立帕肽,12.5 μg,每日2次)治疗的结果进行了比较。在逐渐停用钙剂和维生素D的同时引入rhPTH(1-34)进行治疗转换。比较了rhPTH治疗前和治疗期间的血钙、血磷、碱性磷酸酶以及尿钙肌酐比值(mg/mg)。

结果

rhPTH治疗使2例患者完全停用了钙剂和维生素D,3例患者停用了钙剂,2例患者减少了维生素D剂量。在rhPTH(1-34)治疗期间,血钙、血磷和碱性磷酸酶的平均值无显著变化,而尿钙肌酐比值显著降低(0.55±0.31对0.1±0.1,p=0.02)。与传统治疗相比,4例患者在特立帕肽治疗期间手足搐搦发作次数减少。

结论

在综合征性甲状旁腺功能减退症儿童中,rhPTH(1-34)替代治疗可维持足够的血钙水平,并通过对肾脏的直接作用以及停用钙剂和维生素D治疗,使尿钙排泄迅速恢复正常。

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