Literature DB >> 28819757

Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia.

Mayara Jorgens Prado1,2, Simone Martins de Castro3,2, Cristiane Kopacek3,4, Maricilda Palandi de Mello5, Thaiane Rispoli1,2, Tarciana Grandi1, Cláudia Maria Dornelles da Silva6, Maria Lucia Rosa Rossetti1.   

Abstract

BACKGROUND: Steroid 21-hydroxylase deficiency due to CYP21A2 gene mutations represents more than 90% of all congenital adrenal hyperplasia cases. This deficiency is screened by measuring levels of 17-hydroxyprogesterone, which may vary, causing false positive or false negative results. In order to assist the diagnosis, molecular methodologies have been employed. This work aimed to perform genotyping assays to detect mutations in the CYP21A2 gene and compare the findings with other population studies.
METHODS: The SNaPshot assay was developed to simultaneously detect 12 frequent point mutations in the CYP21A2 gene (p.Arg409Cys, p.Gln319Ter, p.Arg357Trp, p.Leu308PhefsTer6, p.Val237Glu, IVS2-13A/C > G, p.Ile173Asn, p.Pro31Leu, p.Pro454Ser, p.Val282Leu, p.Gly111ValfsTer21 and p.His63Leu). The direct sequencing and multiplex ligation-dependent probe amplification assays were used to confirm point mutations present in the developed method. The latter was also used to search large deletions and gene conversion, complementing the investigation. A total of 166 cases were studied.
RESULTS: The SNaPshot assay was successfully developed to detect the 12 mutations. The results of mutation analysis indicated 84 pathogenic alleles in 48 cases, with p.Val282Leu (27.1%) and IVS2-13A/C > G (20.8%) being the most frequently found mutations. Between the findings of this study and those of other South American studies, there were significant differences in frequency for p.Pro31Leu and p.Val282Leu (p < 0.001). A new variant T in IVS2-13A/C > G was identified in two patients via the SNaPshot assay.
CONCLUSION: The molecular strategy developed for CYP21A2 gene mutation screening allowed us to detect the principle mutations described around the world. Furthermore, the first Southern Brazilian mutation frequencies concerning the CYP21A2 gene were obtained.

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Year:  2017        PMID: 28819757     DOI: 10.1007/s40291-017-0296-6

Source DB:  PubMed          Journal:  Mol Diagn Ther        ISSN: 1177-1062            Impact factor:   4.074


  55 in total

1.  The minisequencing method: an alternative strategy for preimplantation genetic diagnosis of single gene disorders.

Authors:  F Fiorentino; M C Magli; D Podini; A P Ferraretti; A Nuccitelli; N Vitale; M Baldi; L Gianaroli
Journal:  Mol Hum Reprod       Date:  2003-07       Impact factor: 4.025

2.  Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia.

Authors:  Giselle Hayashi; Cláudia Faure; Maria Fernanda Brondi; Carla Vallejos; Daiana Soares; Erica Oliveira; Vinícius N Brito; Berenice B Mendonca; Tânia A S S Bachega
Journal:  Arq Bras Endocrinol Metabol       Date:  2011-11

3.  Enhancements and modifications of primer design program Primer3.

Authors:  Triinu Koressaar; Maido Remm
Journal:  Bioinformatics       Date:  2007-03-22       Impact factor: 6.937

4.  Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.

Authors:  T A Bachega; A E Billerbeck; G Madureira; J A Marcondes; C A Longui; M V Leite; I J Arnhold; B B Mendonca
Journal:  J Clin Endocrinol Metab       Date:  1998-12       Impact factor: 5.958

5.  Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia.

Authors:  Felix Votava; Dóra Török; József Kovács; Dorothea Möslinger; Sabina M Baumgartner-Parzer; János Sólyom; Zuzana Pribilincová; Tadej Battelino; Jan Lebl; Herwig Frisch; Franz Waldhauser
Journal:  Eur J Endocrinol       Date:  2005-06       Impact factor: 6.664

6.  CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations.

Authors:  Nike M M L Stikkelbroeck; Lies H Hoefsloot; Ilse J de Wijs; Barto J Otten; Ad R M M Hermus; Erik A Sistermans
Journal:  J Clin Endocrinol Metab       Date:  2003-08       Impact factor: 5.958

7.  Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia.

Authors:  Shozeb Haider; Barira Islam; Valentina D'Atri; Miriam Sgobba; Chetan Poojari; Li Sun; Tony Yuen; Mone Zaidi; Maria I New
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-28       Impact factor: 11.205

Review 8.  Transcriptomic Segregation of Human Autoantigens Useful for the Diagnosis of Autoimmune Diseases.

Authors:  Peter D Burbelo; Michael J Iadarola; Ilias Alevizos; Matthew R Sapio
Journal:  Mol Diagn Ther       Date:  2016-10       Impact factor: 4.074

Review 9.  Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo
Journal:  Ann Pediatr Endocrinol Metab       Date:  2016-03-31

10.  Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.

Authors:  Nils Krone; Ian T Rose; Debbie S Willis; James Hodson; Sarah H Wild; Emma J Doherty; Stefanie Hahner; Silvia Parajes; Roland H Stimson; Thang S Han; Paul V Carroll; Gerry S Conway; Brian R Walker; Fiona MacDonald; Richard J Ross; Wiebke Arlt
Journal:  J Clin Endocrinol Metab       Date:  2013-01-21       Impact factor: 5.958

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