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      Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

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          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.

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          Most cited references27

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          Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology.

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            One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study.

            Congenital adrenal hyperplasia due to 21-hydroxylase deficiency results in cortisol and aldosterone deficiency and is, in its most severe form, lethal. We aimed to assess the effect of historical medical improvements in the care of patients with this disorder over time and to assess the effects of neonatal screening in Sweden.
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              Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders: Saudi Newborn Screening Program

              To address the implementation of the National Newborn Screening Program (NBS) in Saudi Arabia and stratify the incidence of the screened disorders.
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                Author and article information

                Journal
                J Clin Res Pediatr Endocrinol
                J Clin Res Pediatr Endocrinol
                JCRPE
                Journal of Clinical Research in Pediatric Endocrinology
                Galenos Publishing
                1308-5727
                1308-5735
                March 2019
                20 February 2019
                : 11
                : 1
                : 13-23
                Affiliations
                [1 ]Marmara University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, İstanbul, Turkey
                [2 ]Turkish Directorate of Public Health, Ankara, Turkey
                [3 ]Çukurova University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Adana, Turkey
                [4 ]Necmettin Erbakan University Meram Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Konya, Turkey
                [5 ]Erciyes University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Kayseri, Turkey
                [6 ]Ondokuz Mayıs University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Samsun, Turkey
                [7 ]Osmangazi University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Eskişehir, Turkey
                [8 ]Kocaeli University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Kocaeli, Turkey
                [9 ]Hacettepe University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Ankara, Turkey
                [10 ]İstanbul University İstanbul Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, İstanbul, Turkey
                Author notes
                * Address for Correspondence: Marmara University Faculty of Medicine, Department of Paediatric Endocrinology and Diabetes, Istanbul, Turkey Phone: +90 216 625 45 45 E-mail: tulayguran@ 123456yahoo.com
                Author information
                https://orcid.org/0000-0003-2658-6866
                https://orcid.org/0000-0001-9280-6746
                https://orcid.org/0000-0003-2160-9838
                https://orcid.org/0000-0002-6700-5346
                https://orcid.org/0000-0002-0991-6539
                https://orcid.org/0000-0002-8989-560X
                https://orcid.org/0000-0003-0120-9976
                https://orcid.org/0000-0001-7340-6368
                https://orcid.org/0000-0002-2390-5123
                https://orcid.org/0000-0001-9689-4464
                https://orcid.org/0000-0001-7374-229X
                https://orcid.org/0000-0003-4786-0780
                Article
                19485
                10.4274/jcrpe.galenos.2018.2018.0117
                6398187
                30111524
                4ce3bc4d-0f62-4c8c-a70a-7665f925aa82
                ©Copyright 2019 by Turkish Pediatric Endocrinology and Diabetes Society | The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 May 2018
                : 10 August 2018
                Categories
                Original Article

                Pediatrics
                newborn screening,congenital adrenal hyperplasia,second-tier,steroid profiling
                Pediatrics
                newborn screening, congenital adrenal hyperplasia, second-tier, steroid profiling

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