Clinical and molecular profile of newborns with confirmed or suspicious congenital adrenal hyperplasia detected after a public screening program implementation

Journal Title: Jornal de Pediatria - Year 2019, Vol 95, Issue 3

Abstract

Objective To describe the results obtained in a neonatal screening program after its implementation and to assess the clinical and molecular profiles of confirmed and suspicious congenital adrenal hyperplasia cases. Methods A cross-sectional study was conducted. Newborns with suspected disease due to high 17-hydroxyprogesterone levels and adjusted for birth weight were selected. Classical congenital adrenal hyperplasia (salt-wasting and simple virilizing forms) was diagnosed by an increase in 17-hydroxyprogesterone levels as confirmed in the retest, clinical evaluation, and genotype determined by SNaPshot and multiplex ligation-dependent probe amplification. Results After 24 months, 15 classic congenital adrenal hyperplasia cases were diagnosed in a total of 217,965 newborns, with an estimated incidence of 1:14,531. From 132 patients, seven non-classical and 14 heterozygous patients were screened for CYP21A2 mutations, and 96 patients presented false positives with wild type CYP21A2. On retest, increased 17-hydroxyprogesterone levels were found in classical congenital adrenal hyperplasia patients and showed significant correlation with genotype-related classical genital adrenal hyperplasia. The most frequent mutations were IVS2-13A/C>G followed by gene deletion or rearrangement events in the classical form. In non-classical and heterozygous diseases, p.Val282Leu was the most common mutation. Conclusions The results underscore the effectiveness of congenital adrenal hyperplasia neonatal screening in the public health system and indicate that the adopted strategy was appropriate. The second sample collection along with genotyping of suspected cases helped to properly diagnose both severe and milder cases and delineate them from false positive patients.

Authors and Affiliations

Cristiane Kopacek

Keywords

Related Articles

Assessment of acute motor deficit in the pediatric emergency room

Objectives This review article aimed to present a clinical approach, emphasizing the diagnostic investigation, to children and adolescents who present in the emergency room with acute-onset muscle weakness. Sources A sy...

Prevalence and factors associated with body mass index in children aged 9–11 years

Objective This study aimed to identify the prevalence and factors associated with body mass index (BMI) in children aged 9–11 years. Methods The study is part of the International Study of Childhood Obesity Lifestyle an...

ERICA: smoking is associated with more severe asthma in Brazilian adolescents

Objective To investigate the association between smoking and asthma, and possible associated factors in Brazilian adolescents. Methods A cross-sectional, national, school-based study with adolescents aged 12–17 years, p...

The TyG index cutoff point and its association with body adiposity and lifestyle in children

Objective To investigate the factors associated with insulin resistance in children aged 4–7 years, and to identify the cutoff point of the triglyceride-glucose index for the prediction of insulin resistance in this popu...

Spirometry and volumetric capnography in lung function assessment of obese and normal-weight individuals without asthma

Objective To analyze and compare lung function of obese and healthy, normal-weight children and adolescents, without asthma, through spirometry and volumetric capnography. Methods Cross-sectional study including 77 subj...

Download PDF file
  • EP ID EP575272
  • DOI 10.1016/j.jped.2018.03.003
  • Views 54
  • Downloads 0

How To Cite

Cristiane Kopacek (2019). Clinical and molecular profile of newborns with confirmed or suspicious congenital adrenal hyperplasia detected after a public screening program implementation. Jornal de Pediatria, 95(3), 282-290. https://europub.co.uk/articles/-A-575272