Mulder, Tessa A., Campbell, Purdey J., Taylor, Peter N. ORCID: https://orcid.org/0000-0002-3436-422X, Peeters, Robin P., Wilson, Scott G., Medici, Marco, Dayan, Colin ORCID: https://orcid.org/0000-0002-6557-3462, Jaddoe, Vincent V.W., Walsh, John P., Martin, Nicholas G., Tiemeier, Henning and Korevaar, Tim I.M. 2023. Genetic determinants of thyroid function in children. European journal of endocrinology 189 (2) , pp. 164-174. 10.1093/ejendo/lvad086 |
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Abstract
Objective Genome-wide association studies in adults have identified 42 loci associated with thyroid stimulating hormone (TSH) and 21 loci associated with free thyroxine (FT4) concentrations. While biologically plausible, age-dependent effects have not been assessed. We aimed to study the association of previously identified genetic determinants of TSH and FT4 with TSH and FT4 concentrations in newborns and (pre)school children. Methods We selected participants from three population-based prospective cohorts with data on genetic variants and thyroid function: Generation R (N = 2169 children, mean age 6 years; N = 2388 neonates, the Netherlands), the Avon Longitudinal Study of Parents and Children (ALSPAC; N = 3382, age 7.5 years, United Kingdom), and the Brisbane Longitudinal Twin Study (BLTS; N = 1680, age 12.1 years, Australia). The association of single nucleotide polymorphisms (SNPs) with TSH and FT4 concentrations was studied with multivariable linear regression models. Weighted polygenic risk scores (PRSs) were defined to combine SNP effects. Results In childhood, 30/60 SNPs were associated with TSH and 11/31 SNPs with FT4 after multiple testing correction. The effect sizes for AADAT, GLIS3, TM4SF4, and VEGFA were notably larger than in adults. The TSH PRS explained 5.3%-8.4% of the variability in TSH concentrations; the FT4 PRS explained 1.5%-4.2% of the variability in FT4 concentrations. Five TSH SNPs and no FT4 SNPs were associated with thyroid function in neonates. Conclusions The effects of many known thyroid function SNPs are already apparent in childhood and some might be notably larger in children as compared to adults. These findings provide new knowledge about genetic regulation of thyroid function in early life.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Medicine |
Publisher: | Oxford University Press |
ISSN: | 0804-4643 |
Date of First Compliant Deposit: | 5 October 2023 |
Date of Acceptance: | 6 June 2023 |
Last Modified: | 07 Oct 2023 02:33 |
URI: | https://orca.cardiff.ac.uk/id/eprint/162972 |
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