Volume 2013 Supplement 1

7th Asia Pacific Paediatric Endocrine Society (APPES) Biennial Scientific Meeting

Open Access

Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency

  • Vu Chi Dung1,
  • Tran Van Khanh2,
  • Maki Fukami3,
  • Le Thi Phuong2,
  • Nguyen Thi Ha2,
  • Nguyen Thanh Liem1 and
  • Ta Thanh Van2
International Journal of Pediatric Endocrinology20132013(Suppl 1):P128

DOI: 10.1186/1687-9856-2013-S1-P128

Published: 3 October 2013

Congenital adrenal hyperplasia (CAH) is one of the most common inherited metabolic disorders. It includes a group of autosomal recessive disorders caused by the deficiency of one of the enzymes involed in one of the various steps of adrenal steroid synthesis. The most common form of CAH (95%) is caused by mutations in CYP21A2, the gene encoding the adrenal steroid 21-hydroxylase enzyme (P450c21). Two major phenotype are recognized in 21-OHD: classic and non-classic. Classic CAH is clinically categorized in two groups: the simple-virilising and the salt-wasting form. The National Hospital of Pediatrics (NHP) in Hanoi is an 1100 bed tertiary referral centre servicing approximately 30 million people from northern provinces of Vietnam. At the start of 1999 there were 91 children with CAH due to 21-hydroxylase deficiency (21-OHD) managed at NHP. By June 2012 this increased to 624 [98.2% due to 21-OHD], representing a more than six fold increase over 12 years. Number of new cases ranged from 40 to 70 per year.

We aim to determine the mutations in the CYP21A2 gene in Vietnamese patients with CAH and attempt a genotype-phenotype correlation. Molecular analysis was performed using PCR, multiplex ligation-dependent probe amplification and direct sequencing of PCR products of the CYP21A2 gene in 81 CAH patients (39 male and 42 female). Correlation between phenotype and genotype was evaluated based on identified mutations and clinical manifestations.

Mutations were identified in 92.6% mutant alleles, 22 genotypes were found in 81 cases. Seven different causative mutations were identified in CYP21A2 including one novel mutation. The most frequent genetic defect in the classic salt-wasting and simple virilizing forms was the IVS2-13A/C>G (54 alleles; 36%) mutation, followed by Large lesion (42 alleles; 28%) including exon 1 deletion (2 alleles), exon 1-3 deletion (10 alleles), exon 1-6 deletion (4 alleles), exon 1-8 deletion (2 alleles) and larger deletion (24 alleles); p.R356W (26 alleles; 17.3%); p.l172N (15 alleles; 10%). The rarer mutations were novel one p.R484fsX541 (6 alleles; 4%); p.Q318X (4 alleles; 2.7%) and p.R426C (3 alleles; 2%). The majority of patients (61 cases; 75.3%) were homozygotes. Four cases were compound heterozygous. Thirteen patients had only a heterozygous mutation detected. Genotype accurately predicted phenotype in 93.8 and 100% of patients with salt-wasting and simple virilizing, respectively.

The spectrum of mutations of the CYP21A2 gene in Vietnamese patients is comparable to the some reported in other Asian population. Large deletion accounts for nearly one-third of the genetic defects. Therefore, laboratory should include methods for detecting point mutations as well as large deletions. Genotype-Phenotype correlation was high in the studied patients.

Authors’ Affiliations

(1)
Vietnam National Hospital of Pediatrics
(2)
Hanoi Medical University
(3)
National Research Institute for Child Health and Development

Copyright

© Dung et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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