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Makale detayı · 2025

The First-year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-hydroxylase Deficiency and a Higher Detection Rate of Non-classical Cases

Journal of Clinical Research in Pediatric Endocrinology

YÖKSİS OpenAlex ISSN 1308-5727 DOI 10.4274/jcrpe.galenos.2025.2024-9-11 Atıf 0 Açık erişim · gold SJR Q2 JCR Q2 TR Index

10.4274/jcrpe.galenos.2025.2024-9-11

YÖKSİS YÖKSİS makale kaydı

OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

OpenAlex kaydı

İngilizce (OpenAlex)

Objective: Neonatal screening for congenital adrenal hyperplasia (CAH) was implemented nationwide in Türkiye in 2022. The performance of this screening program in its first year was assessed. Methods: This retrospective, descriptive study included neonates born in Türkiye between January 1 and December 31, 2022, with gestational age ≥32 weeks and birth weight ≥1500 grams. The screening protocol used a two-tier approach. In the first step, 17α-hydroxyprogesterone (17-OHP) levels were measured using fluoroimmunoassay (FIA) in dried blood spots (DBS) collected at 3-5 days of life. Infants with positive results underwent second-tier testing using liquid chromatography-tandem mass spectrometry to measure 17-OHP, 21-deoxycortisol (21-DF), cortisol (F), and 11-deoxycortisol (S) in DBS. Those with a steroid ratio (21-DF+17-OHP)/F ≥1 were referred to pediatric endocrinology clinics for diagnostic evaluation. Results: Of 1,096,069 neonates screened (including 149,652 refugees), second-tier tests were performed on 70,455 (6.88%) infants, and 3,429 (0.27%) were referred to clinics, resulting in 91 confirmed cases of classical 21-hydroxylase deficiency (21-OHD) CAH (77; salt-wasting, 14; simple virilizing). Twenty-two patients were diagnosed with non-classical 21-OHD CAH. The frequency of classical 21-OHD was 1 in 12,044. The first-tier FIA-17-OHP values were below 17.5 ng/mL in 99.8% of healthy neonates with ≥36 weeks gestation or ≥2500 grams and below 50 ng/mL in those with 32-36 weeks or 1500-2500 grams. Conclusion: Neonatal CAH screening facilitates early diagnosis of 21-OHD and improved patient care. Using refined cut-offs may reduce referrals six-fold and eliminate second-tier testing for 95% of infants. Ongoing evaluation can enhance the efficiency and cost-effectiveness of the screening protocol.

OpenAlex zenginleştirmesi

Konular

  • Sexual Differentiation and Disorders
  • Metabolism and Genetic Disorders
  • Hormonal and reproductive studies

Tür: article Sexual Differentiation and Disorders

İndeks bilgisi

WoS (JCR) ve Scopus (SJR) çeyrekleri ISSN ve yayın yılına göre. · 2025

Scopus (SJR) / WoS (JCR)

JCRPE Journal of Clinical Research in Pediatric Endocrinology

Scopus (SJR) Q2 0,599 2025 yılı
WoS (JCR) Q2 JIF 1,9 2025 yılı

TR Index

Journal of Clinical Research in Pediatric Endocrinology

TR Index yılları 2015–2026 (12)

Makale yılı TR Index kapsamında.

Üniversiteler

  • AYDIN ADNAN MENDERES ÜNİVERSİTESİ

Yazarlar

  1. TÜLAY GÜRAN
  2. Elif Yürüker
  3. AHMET ANIK AYDIN ADNAN MENDERES ÜNİVERSİTESİ
  4. MÜGE ATAR
  5. EMİNE ÇAMTOSUN
  6. ELİF EVİZ
  7. MEHMET İSAKOCA
  8. EDA MENGEN UÇAKTÜRK
  9. BUŞRA GÜRPINAR TOSUN
  10. İHSAN TURAN
  11. AYLİN KILINÇ UĞURLU
  12. EDİP UNAL
  13. DOĞUŞ VURALLI KARAOĞLAN
  14. GÜLAY CAN YILMAZ
  15. YÜKSEL HAKAN AYDOĞMUŞ
  16. ŞÜKRAN DARCAN