Detecting congenital hypothyroidism with newborn screening: the relevance of thyroid‐stimulating hormone cutoff values

Objectives: To assess the prevalence of congenital hypothyroidism and the ability of various neonatal thyroid‐stimulating hormone (TSHneo) cutoff values to detect this disease. Methods: This cohort study was based on the retrospective collection of information available from the Reference Service fo...

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Bibliographic Details
Main Authors: Stela Maris Silvestrin, Claudio Leone, Cléa Rodrigues Leone
Format: Article
Language:Portuguese
Published: Brazilian Society of Pediatrics 2017-05-01
Series:Jornal de Pediatria (Versão em Português)
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Online Access:http://www.sciencedirect.com/science/article/pii/S2255553617300010
Description
Summary:Objectives: To assess the prevalence of congenital hypothyroidism and the ability of various neonatal thyroid‐stimulating hormone (TSHneo) cutoff values to detect this disease. Methods: This cohort study was based on the retrospective collection of information available from the Reference Service for Newborn Screening database for all live births from January 1, 2010, to December 31, 2012, assessed using the Newborn Screening Program of a Brazilian state. The infants were divided into two groups: I–Control: infants with normal newborn screening tests and II–Study: infants with congenital hypothyroidism. Analysis included comparing the TSHneo levels from both groups. A receiver operating characteristic (ROC) curve was constructed to assess the TSHneo cutoff values. Results: Using a TSHneo cutoff value of 5.0 μIU/mL, 50 out of 111,705 screened infants had diagnosis of congenital hypothyroidism (prevalence 1:2234 live births). The ROC curve showed that TSHneo value of 5.03 μIU/mL had 100% sensitivity and the greatest associated specificity (93.7%). The area under the curve was 0.9898 (p < 0.0001). Conclusions: The ROC curve confirmed that the TSHneo cutoff value of 5.0 μIU/mL adopted by the Newborn Screening Program of a Brazilian state was the most appropriate for detecting congenital hypothyroidism and most likely explains the high prevalence that was found.
ISSN:2255-5536