Multi-omics investigation of thyroid development and dysfunction in down syndrome

TL;DR

This study explores how Down syndrome affects thyroid development and function through multi-omics analysis of fetal thyroid tissue.

Contribution

The study identifies gene expression and DNA methylation changes in Down syndrome fetal thyroid tissue linked to thyroid dysfunction.

Findings

DS fetal thyroid tissue shows underdevelopment with smaller follicles and greater heterogeneity.

Three thyroid-related genes (FOXE1, IYD, DIO2) are significantly downregulated in DS tissue.

Genome-wide gene expression and DNA methylation changes suggest gene dosage and epigenetic effects in DS.

Abstract

Down syndrome (DS), caused by trisomy of chromosome 21, is associated with a high prevalence of congenital non-autoimmune thyroid dysfunction, typically characterized by an elevated serum thyroid stimulating hormone (TSH) concentration. Early-life observational studies and fetal cordocentesis data, consistently reporting elevated TSH levels, suggest a developmental origin. However, the underlying pathophysiological mechanism remains unclear. This study aimed to investigate the molecular and developmental features underlying thyroid dysfunction in DS.

Thyroid tissue of fetuses with DS (n = 4) and fetuses without a genetic/developmental abnormality (n = 5) were analyzed using histology, bulk RNA sequencing (RNA-seq), and DNA methylation (DNAm) profiling.

Histological analysis revealed underdevelopment of DS fetal thyroid tissue, with smaller follicles and greater heterogeneity. RNA-seq identified 1035 differentially expressed genes (DEGs) distributed across the genome. Notably, three thyroid-relevant genes, FOXE1, IYD, and DIO2, were significantly downregulated in DS tissue. Gene set enrichment analysis (GSEA) showed widespread disruption of cellular processes. DNAm analysis identified 266 differentially methylated regions (DMRs), several of which overlapped with loci previously implicated in DS. Integration of expression and DNAm data revealed 20 significant integrative methylation–expression analysis associations, indicating cis-regulatory DNAm effects on gene expression.

These findings suggest that congenital thyroid dysfunction in DS represents a DS-specific form of thyroid dysfunction, characterized by impaired thyroid development and altered expression and regulation of genes involved in thyroid function and general cellular processes. The genome-wide molecular changes observed likely result from gene dosage effects and systemic (epi)genomic disturbances caused by trisomy 21.

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