Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism.

Abstract

OBJECTIVES:

Iodide transport defect (ITD) is one of the principal causes of congenital hypothyroidism (CH) and its primary molecular mechanism is a mutation of the sodium/iodide symporter (NIS) gene. This study aims to analyse the clinical characteristics and genetic mutations of ITD.

METHODS:

The participants were a pair of siblings diagnosed with congenital hypothyroidism. Inductively coupled plasma mass spectrometry was used to determine the concentration of salivary iodine and serum iodine and to calculate their ratio. At the same time, next-generation sequencing (NGS) was applied to detect all exons of congenital hypothyroidism-related genes. All suspicious variants were further validated in the patients and their parents by PCR and Sanger sequencing.

RESULTS:

Both patients were conclusively diagnosed with thyroid iodine transport defect (ITD). NGS identified two variants of the NIS gene in the siblings: c.1021G>A (p.Gly341Arg) with paternal origin and c.1330-2A>C with maternal origin. Both of these variants have not been reported to date. They are predicted to be pathogenic based on these clinical symptoms and comprehensive software analysis.

CONCLUSIONS:

This is the first reported family study of congenital hypothyroidism with SLC5A5 mutation in China. Next-generation sequencing technology is an effective means of studying the genetics of congenital hypothyroidism. The therapeutic effect of potassium iodide needs to be further evaluated.

• Authors: Lifei Gong, Nan Yang, Jinqi Zhao, Yue Tang, Lulu Li, Haihe Yang, Yuanyuan Kong
• Journal: Journal of pediatric endocrinology & metabolism : JPEM (J Pediatr Endocrinol Metab) Vol. 35 Issue 6 Pg. 741-748 (Jun 27 2022) ISSN: 2191-0251 [Electronic] Germany
• PMID: 35438852 (Publication Type: Journal Article)
• Copyright: © 2022 Walter de Gruyter GmbH, Berlin/Boston.

Chemical References

• Iodides
• Iodine

Topics

• Congenital Hypothyroidism (diagnosis, drug therapy, genetics)
• Humans
• Iodides (therapeutic use)
• Iodine
• Metabolism, Inborn Errors (genetics)
• Mutation