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活性维生素 D 治疗中国人假性维生素 D 缺乏性佝偻病(PDDR)的基因突变更新和长期结果。

Mutation update and long-term outcome after treatment with active vitamin D in Chinese patients with pseudovitamin D-deficiency rickets (PDDR).

机构信息

Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Shuaifuyuan No. 1, Wangfujing, Dongcheng District, Beijing, 100730, China.

出版信息

Osteoporos Int. 2019 Feb;30(2):481-489. doi: 10.1007/s00198-018-4607-5. Epub 2018 Oct 31.

Abstract

UNLABELLED

Pseudovitamin D-deficiency rickets is a rare disease which is caused by CYP27B1. In this study, we identified 9 mutations in 7 PDDR patients. In addition, we observed the response to long-term treatment of calcitriol in 15 Chinese patients with PDDR, which showed that the biochemical abnormalities had been corrected satisfactorily after 1-year treatment.

INTRODUCTION

Pseudovitamin D-deficiency rickets is a rare autosomal recessive disorder resulting from a defect in 25-hydroxyvitamin D 1α-hydroxylase, which is encoded by CYP27B1. The purpose of this study was to identify the CYP27B1 mutations and investigate the response to long-term treatment of calcitriol in Chinese patients with PDDR.

METHODS

We investigated CYP27B1 mutations in seven individuals from six separate families. To investigate the response to long-term (13 years) treatment with calcitriol in PDDR patients, we additionally collected clinical data of eight families from our previous report and analyzed their biochemical parameter and radiographic changes during the treatment.

RESULTS

Nine different mutations were identified: two novel missense mutations (G194R, R259L), three novel and one reported deletion mutations (c1442delA, c1504delA, c311-321del, and c. 48-60del), two novel nonsense mutations (c.85G>T, c.580G>T), and a reported insertion mutation (c1325-1332insCCCACCC). The statistical analysis revealed that parathyroid hormone (PTH) and ALP significantly decreased after 6-month and 1-year treatment with calcitriol respectively. Urine calcium was measured in all the patients without kidney stones being documented. After 6-year treatment, the radiographic abnormalities had also been improved. Two patients who had reached their final height are both with short stature (height Z-score below - 2.0).

CONCLUSIONS

We identified seven novel mutations of CYP27B1 gene in seven Chinese PDDR families. Our findings revealed after 1-year treatment of active vitamin D, PTH and ALP significantly decreased. The correction of the biochemical abnormalities had not improved the final height satisfactorily.

摘要

未注明

假性维生素 D 缺乏性佝偻病是一种罕见的疾病,由 CYP27B1 引起。在这项研究中,我们在 7 名 PDDR 患者中鉴定了 9 种突变。此外,我们观察了 15 名中国 PDDR 患者长期接受骨化三醇治疗的反应,结果表明,经过 1 年的治疗,生化异常得到了满意的纠正。

介绍

假性维生素 D 缺乏性佝偻病是一种罕见的常染色体隐性遗传病,由 25-羟维生素 D1α-羟化酶缺陷引起,该酶由 CYP27B1 编码。本研究的目的是鉴定 CYP27B1 突变,并研究中国 PDDR 患者长期(13 年)接受骨化三醇治疗的反应。

方法

我们研究了来自 6 个不同家庭的 7 个人的 CYP27B1 突变。为了研究 PDDR 患者长期(13 年)接受骨化三醇治疗的反应,我们还收集了我们之前报告的 8 个家庭的临床数据,并分析了他们在治疗过程中的生化参数和影像学变化。

结果

鉴定了 9 种不同的突变:2 种新的错义突变(G194R,R259L),3 种新的和 1 种报道的缺失突变(c1442delA,c1504delA,c311-321del,和 c.48-60del),2 种新的无义突变(c.85G>T,c.580G>T),和 1 种报道的插入突变(c1325-1332insCCCACCC)。统计分析显示,甲状旁腺激素(PTH)和 ALP 在骨化三醇治疗 6 个月和 1 年后分别显著下降。所有患者均测量尿钙,无肾结石记录。治疗 6 年后,影像学异常也得到改善。达到最终身高的 2 名患者均身材矮小(身高 Z 评分低于-2.0)。

结论

我们在 7 个中国 PDDR 家族中鉴定了 CYP27B1 基因的 7 个新突变。我们的发现表明,在接受活性维生素 D 治疗 1 年后,PTH 和 ALP 显著下降。生化异常的纠正并不能使最终身高得到满意的改善。

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