Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2020

Open Access 01-12-2020 | Rickets | Research

Clinical and genetic analysis of two Chinese families with vitamin D-dependent rickets type IA and follow-up

Authors: Yunfei Li, Xin Yuan, Ruimin Chen, Xiangquan Lin, Huakun Shangguan, Xiaohong Yang, Ying Zhang

Published in: Orphanet Journal of Rare Diseases | Issue 1/2020

Login to get access

Abstract

Objective

Vitamin D-dependent rickets type IA (VDDR-IA) is a rare autosomal recessive disorder characterized by the early onset of severe rickets. The objectives of this study were twofold: (1) to analyze the clinical characteristics and therapy of two patients with VDDR-IA from two separate Chinese families, and (2) investigate the CYP27B1 gene mutations in two large pedigrees.

Methods

Medical history, clinical manifestations, physical examination, radiological findings and laboratory data were analyzed from two patients with VDDR-IA. Serum 1, 25-dihydroxyvitamin D [1, 25-(OH)2D3] of the two patients and their respective families were measured by ELISA and blood samples from both families was obtained for CYP27B1 gene sequence.

Results

Two patients had typical manifestations and radiological evidence of rickets. Laboratory data showed hypocalcaemia and hypophosphataemia, along with high levels of serum alkaline phosphatase, parathyroid hormone and 25-hydroxyvitamin D3. However, serum 1,25-(OH)2D3 level were low in the patients but normal in their family members. Genetic sequence identified two patients were homozygous for a duplication mutation in exon 8 of CYP27B1 gene (c.1319_1325dupCCCACCC, p.Phe443Profs * 24). After treating with calcitriol and calcium, there was biochemical improvement with normalization of serum calcium and phosphorus, and radiographic evidence of compensatory skeletal mineralization. One patient developed nephrocalcinosis during follow-up.

Conclusions

This study identified a recurrent seven-nucleotide insertion of CYP27B1 in two large pedigrees, and compared the clinical characteristics and individual therapy of two affected patients. Additionally, our experience further supports the notion that nephrocalcinosis can occur even on standard doses of calcitriol and oral calcium, and normal level of serum calcium, phosphorus, PTH and 25-(OH)D3.
Literature
2.
go back to reference Fu GK, Lin D, Zhang MY, Bikle DD, Shackleton CH, et al. Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. Mol Endocrinol. 1997;11:1961–70.PubMed Fu GK, Lin D, Zhang MY, Bikle DD, Shackleton CH, et al. Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. Mol Endocrinol. 1997;11:1961–70.PubMed
3.
go back to reference Haussler MR, Whitfield GK, Kaneko I, Haussler CA, Hsieh D, et al. Molecular mechanisms of vitamin D action. Calcif Tissue Int. 2013;92:77–98.CrossRef Haussler MR, Whitfield GK, Kaneko I, Haussler CA, Hsieh D, et al. Molecular mechanisms of vitamin D action. Calcif Tissue Int. 2013;92:77–98.CrossRef
4.
go back to reference Miller WL, Portale AA. Vitamin D biosynthesis and vitamin D 1 alpha-hydroxylase deficiency. Endocr Dev. 2003;6:156–74.CrossRef Miller WL, Portale AA. Vitamin D biosynthesis and vitamin D 1 alpha-hydroxylase deficiency. Endocr Dev. 2003;6:156–74.CrossRef
5.
go back to reference Prader A, Illig R, Heierli E. An unusual form of primary vitamin D-resistant rickets with hypocalcemia and autosomal-dominant hereditary transmission: hereditary pseudo-deficiency rickets. Helv Paediatr Acta. 1961;16:452–68.PubMed Prader A, Illig R, Heierli E. An unusual form of primary vitamin D-resistant rickets with hypocalcemia and autosomal-dominant hereditary transmission: hereditary pseudo-deficiency rickets. Helv Paediatr Acta. 1961;16:452–68.PubMed
6.
go back to reference Wang X, Zhang MY, Miller WL, Portale AA. Novel gene mutations in patients with 1alpha-hydroxylase deficiency that confer partial enzyme activity in vitro. J Clin Endocrinol Metab. 2002;87:2424–30.PubMed Wang X, Zhang MY, Miller WL, Portale AA. Novel gene mutations in patients with 1alpha-hydroxylase deficiency that confer partial enzyme activity in vitro. J Clin Endocrinol Metab. 2002;87:2424–30.PubMed
7.
go back to reference Alzahrani AS, Zou M, Baitei EY, Alshaikh OM, Al-Rijjal RA, et al. A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1. J Clin Endocrinol Metab. 2010;95:4176–83.CrossRef Alzahrani AS, Zou M, Baitei EY, Alshaikh OM, Al-Rijjal RA, et al. A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1. J Clin Endocrinol Metab. 2010;95:4176–83.CrossRef
8.
go back to reference Cao L, Liu F, Wang Y, Ma J, Wang S, et al. Novel vitamin D 1alpha-hydroxylase gene mutations in a Chinese vitamin-D-dependent rickets type I patient. J Genet. 2011;90:339–42.CrossRef Cao L, Liu F, Wang Y, Ma J, Wang S, et al. Novel vitamin D 1alpha-hydroxylase gene mutations in a Chinese vitamin-D-dependent rickets type I patient. J Genet. 2011;90:339–42.CrossRef
9.
go back to reference Durmaz E, Zou M, Al-Rijjal RA, Bircan I, Akçurin S, Meyer B, Shi Y. Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A. Clin Endocrinol (Oxf). 2012;77:363–9.CrossRef Durmaz E, Zou M, Al-Rijjal RA, Bircan I, Akçurin S, Meyer B, Shi Y. Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A. Clin Endocrinol (Oxf). 2012;77:363–9.CrossRef
10.
go back to reference Babiker AM, Al Gadi I, Al-Jurayyan NA, Al Nemri AM, Al Haboob AA, Al Boukai AA, Al Zahrani A, Habib HA. A novel pathogenic mutation of the CYP27B1 gene in a patient with vitamin D-dependent rickets type 1: a case report. BMC Res Notes. 2014;7:783.CrossRef Babiker AM, Al Gadi I, Al-Jurayyan NA, Al Nemri AM, Al Haboob AA, Al Boukai AA, Al Zahrani A, Habib HA. A novel pathogenic mutation of the CYP27B1 gene in a patient with vitamin D-dependent rickets type 1: a case report. BMC Res Notes. 2014;7:783.CrossRef
11.
go back to reference Cui N, Xia W, Su H, Pang L, Jiang Y, Sun Y, et al. Novel mutations of CYP27B1 gene lead to reduced activity of 1alpha-hydroxylase in Chinese patients. Bone. 2012;51:563–9.CrossRef Cui N, Xia W, Su H, Pang L, Jiang Y, Sun Y, et al. Novel mutations of CYP27B1 gene lead to reduced activity of 1alpha-hydroxylase in Chinese patients. Bone. 2012;51:563–9.CrossRef
12.
go back to reference Cui N, Xia W, Su H, Pang L, Jiang Y, Sun Y, Nie M, Xing X, Li M, Wang O, Yuan T, Chi Y, Hu Y, Liu H, Meng X, Zhou X. A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A. J Pediatr Endocrinol Metab. 2014;27:335–41. Cui N, Xia W, Su H, Pang L, Jiang Y, Sun Y, Nie M, Xing X, Li M, Wang O, Yuan T, Chi Y, Hu Y, Liu H, Meng X, Zhou X. A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A. J Pediatr Endocrinol Metab. 2014;27:335–41.
13.
go back to reference Sawada N, Sakaki T, Kitanaka S, Kato S, Inouye K. Structure-function analysis of CYP27B1 and CYP27A1. Studies on mutants from patients with vitamin D-dependent rickets type I (VDDR-I) and cerebrotendinous xanthomatosis (CTX). Eur J Biochem. 2001;268:6607–15.CrossRef Sawada N, Sakaki T, Kitanaka S, Kato S, Inouye K. Structure-function analysis of CYP27B1 and CYP27A1. Studies on mutants from patients with vitamin D-dependent rickets type I (VDDR-I) and cerebrotendinous xanthomatosis (CTX). Eur J Biochem. 2001;268:6607–15.CrossRef
14.
go back to reference Donghi V, Di Frenna M, di Lascio A, Chiumello G, Weber G. Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports. J Pediatr Endocrinol Metab. 2011;24:801–5.CrossRef Donghi V, Di Frenna M, di Lascio A, Chiumello G, Weber G. Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports. J Pediatr Endocrinol Metab. 2011;24:801–5.CrossRef
15.
go back to reference Brame LA, White KE, Econs MJ. Renal phosphate wasting disorders: clinical features and pathogenesis. Semin Nephrol. 2004;24:39–47.CrossRef Brame LA, White KE, Econs MJ. Renal phosphate wasting disorders: clinical features and pathogenesis. Semin Nephrol. 2004;24:39–47.CrossRef
16.
go back to reference Yuan B, Xing Y, Horst RL, Drezner MK. Evidence for abnormal translational regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase activity in the hyp-mouse. Endocrinology. 2004;145:3804–12.CrossRef Yuan B, Xing Y, Horst RL, Drezner MK. Evidence for abnormal translational regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase activity in the hyp-mouse. Endocrinology. 2004;145:3804–12.CrossRef
17.
go back to reference Kitanaka S, Takeyama K, Murayama A, Kato S. The molecular basis of vitamin D-dependent rickets type I. Endocr J. 2001;48:427–32.CrossRef Kitanaka S, Takeyama K, Murayama A, Kato S. The molecular basis of vitamin D-dependent rickets type I. Endocr J. 2001;48:427–32.CrossRef
18.
go back to reference Sahay M, Sahay R. Rickets-vitamin D deficiency and dependency. Indian J Endocrinol Metab. 2012a;16:164–76.CrossRef Sahay M, Sahay R. Rickets-vitamin D deficiency and dependency. Indian J Endocrinol Metab. 2012a;16:164–76.CrossRef
19.
go back to reference Sahay M, Sahay R. Renal rickets-practical approach. Indian J Endocrinol Metab. 2012b;17(Suppl 1):S35-44. Sahay M, Sahay R. Renal rickets-practical approach. Indian J Endocrinol Metab. 2012b;17(Suppl 1):S35-44.
20.
go back to reference Wang JT, Lin CJ, Burridge SM, Fu GK, Labuda M, Portale AA, Miller WL. Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families. Am J Hum Genet. 1998;63:1694–702.CrossRef Wang JT, Lin CJ, Burridge SM, Fu GK, Labuda M, Portale AA, Miller WL. Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families. Am J Hum Genet. 1998;63:1694–702.CrossRef
21.
go back to reference Ito N, Peña AS, Perano S, Atkins GJ, Findlay DM, Couper JJ. First Australian report of vitamin D-dependent rickets type I. Med J Aust. 2014;201:420–1.CrossRef Ito N, Peña AS, Perano S, Atkins GJ, Findlay DM, Couper JJ. First Australian report of vitamin D-dependent rickets type I. Med J Aust. 2014;201:420–1.CrossRef
22.
go back to reference Labuda M, Fujiwara TM, Ross MV, Morgan K, Garcia-Heras J, Ledbetter DH, Hughes MR, Glorieux FH. Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14. J Bone Miner Res. 1992;7:1447–53.CrossRef Labuda M, Fujiwara TM, Ross MV, Morgan K, Garcia-Heras J, Ledbetter DH, Hughes MR, Glorieux FH. Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14. J Bone Miner Res. 1992;7:1447–53.CrossRef
23.
go back to reference Delvin EE, Glorieux FH, Marie PJ, Pettifor JM. Vitamin D dependency: replacement therapy with calcitriol? J Pediatr. 1981;99:26–34.CrossRef Delvin EE, Glorieux FH, Marie PJ, Pettifor JM. Vitamin D dependency: replacement therapy with calcitriol? J Pediatr. 1981;99:26–34.CrossRef
24.
go back to reference Laway BA, Wani AI, Masoodi SR, Bashir MI, Ganie MA, Zargar AH. Hypercalciuria and nephrolithiasis on long-term follow-up of pseudo-vitamin D deficiency rickets. J Pak Med Assoc. 2010;60(7):591–3.PubMed Laway BA, Wani AI, Masoodi SR, Bashir MI, Ganie MA, Zargar AH. Hypercalciuria and nephrolithiasis on long-term follow-up of pseudo-vitamin D deficiency rickets. J Pak Med Assoc. 2010;60(7):591–3.PubMed
25.
go back to reference Yan Y, Calikoglu AS, Jain N. Vitamin D-dependent rickets type 1: a rare, but treatable, cause of severe hypotonia in infancy. J Child Neurol. 2011;26:1571–5.CrossRef Yan Y, Calikoglu AS, Jain N. Vitamin D-dependent rickets type 1: a rare, but treatable, cause of severe hypotonia in infancy. J Child Neurol. 2011;26:1571–5.CrossRef
26.
go back to reference Rowling MJ, Gliniak C, Welsh J, Fleet JC. High dietary vitamin D prevents hypocalcemia and osteomalacia in CYP27B1 knockout mice. J Nutr. 2007;137:2608–15.CrossRef Rowling MJ, Gliniak C, Welsh J, Fleet JC. High dietary vitamin D prevents hypocalcemia and osteomalacia in CYP27B1 knockout mice. J Nutr. 2007;137:2608–15.CrossRef
Metadata
Title
Clinical and genetic analysis of two Chinese families with vitamin D-dependent rickets type IA and follow-up
Authors
Yunfei Li
Xin Yuan
Ruimin Chen
Xiangquan Lin
Huakun Shangguan
Xiaohong Yang
Ying Zhang
Publication date
01-12-2020
Publisher
BioMed Central
Keyword
Rickets
Published in
Orphanet Journal of Rare Diseases / Issue 1/2020
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-020-01558-7

Other articles of this Issue 1/2020

Orphanet Journal of Rare Diseases 1/2020 Go to the issue