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Neonatal screening for congenital adrenal hyperplasia in turkey: A pilot study with 38,935 infants

  • Tülay Güran
  • , Başak Tezel
  • , Fatih Gürbüz
  • , Beray Selver Eklioğlu
  • , Nihal Hatipoğlu
  • , Cengiz Kara
  • , Enver Şimşek
  • , Filiz Mine Çizmecioğlu
  • , Alev Ozon
  • , Firdevs Baş
  • , Murat Aydın
  • , Feyza Darendeliler
  • Marmara University
  • General Directorate of Public Health
  • Cukurova University
  • Necmettin Erbakan University
  • Erciyes University
  • Ondokuz Mayis University
  • Osmangazi University
  • Kocaeli University
  • Istanbul University

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

Objective: Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. In this study, our aim was to estimate the incidence of CAH in Turkey and to assess the characteristics and efficacy of the adopted newborn CAH screening strategy. Methods: A pilot newborn CAH screening study was carried out under the authority of the Turkish Directorate of Public Health. Newborn babies of ≥32 gestational weeks and ≥1500 gr birth weight from four cities, born between March 27-September 15, 2017 were included in the study. Screening protocol included one sample two-tier testing. In the first step, 17α-hydroxyprogesterone (17-OHP) was measured by fluoroimmunoassay in dried blood spots (DBS) obtained at 3-5 days of life. The cases with positive initial screening were tested by steroid profiling in DBS using a liquid chromatography-tandem mass spectrometry method to measure 17-OHP, 21-deoxycortisol (21-S), cortisol (F), 11-deoxycortisol and androstenedione as a second-tier test. The babies with a steroid ratio (21-S+17-OHP)/F of ≥0.5 were referred to pediatric endocrinology clinics for diagnostic assessment. Results: 38,935 infants were tested, 2265 (5.82%) required second-tier testing and 212 (0.54%) were referred for clinical assessment, six of whom were diagnosed with CAH (four males, two females). Four cases were identified as SW 21-hydroxylase deficiency (21-OHD) (two males, two females). One male baby had simple virilizing 21-OHD and one male baby had 11-OHD CAH. The incidence of classical 21-OHD in the screened population was 1:7,787. Conclusion: The incidence of CAH due to classical 21-OHD is higher in Turkey compared to previous reports. We, therefore, suggest that CAH be added to the newborn screening panel in Turkey. The use of steroid profiling as a second-tier test was found to improve the efficacy of the screening and reduce the number of false-positives.

Original languageEnglish
Pages (from-to)13-23
Number of pages11
JournalJCRPE Journal of Clinical Research in Pediatric Endocrinology
Volume11
Issue number1
DOIs
Publication statusPublished - Mar 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Congenital adrenal hyperplasia
  • Newborn screening
  • Second-tier
  • Steroid profiling

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