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Updated: May 31, 2026

An Ex vivo Culture System to Study Thyroid Development
Published on: June 6, 2014
Correct neonatal free thyroxine reference intervals are crucial to detect central congenital hypothyroidism
Mark R Garrelfs1,2, Peter Lauffer1,2,3, Jacquelien J Hillebrand2,4
1Department of Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Centers, European Reference Network on Rare Endocrine Conditions (Endo-ERN), University of Amsterdam and Vrije Universiteit, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.
Objective:
In the Netherlands, after an abnormal newborn screening (NBS) result suggestive of central congenital hypothyroidism (CH), children are referred for confirmatory plasma-free thyroxine (fT4) measurement. Correct interpretation of these results relies on appropriate age- and assay-specific reference intervals (RI), which are often not available. The current study was performed to check whether the use of adult or other incorrect fT4 RIs during the post-screening work-up of neonates with an abnormal NBS had led to missed diagnoses of central CH.
Design:
Retrospective cohort study with prospective re-evaluation.
Methods:
Children born between 1 March 2018 and 1 April 2021 with an abnormal NBS result suggesting central CH were identified through the Dutch national screening registry (NEORAH). Children classified as having a "false positive" screening result based on post-screening confirmatory fT4 concentrations in the neonatal period were included if those fT4 concentrations were ≤ 3 pmol/L above the assay-specific lower limit of the adult RI. After obtaining informed consent, re-evaluation of thyroid function was performed.
Results:
Six children were identified and informed consent was obtained from four participants. Two out of four participants received a new diagnosis of central CH, including one case of multiple pituitary hormone deficiencies (MPHD).
Conclusions:
This study highlights the critical need for age- and assay-specific RIs for plasma fT4 to accurately diagnose central CH in the neonatal period.
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