A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

Loading...
Thumbnail Image
Files
journal.pgen.1003266.s001.TIF(722.64 KB)
Additional File 1: Figure S1.
journal.pgen.1003266.s002.TIF(1.54 MB)
Additional File 2: Figure S2.
journal.pgen.1003266.s003.PDF(618.07 KB)
Additional File 3: Figure S3.
journal.pgen.1003266.s004.XLS(372.5 KB)
Additional File 4: Table S1.
Date
2013
Authors
Porcu, Eleonora
Medici, Marco
Pistis, Giorgio
Volpato, Claudia B.
Wilson, Scott G.
Cappola, Anne R.
Bos, Steffan D.
Deelen, Joris
den Heijer, Martin
Freathy, Rachel M.
Journal Title
Journal ISSN
Volume Title
Publisher
Public Library of Science
Research Projects
Organizational Units
Journal Issue
Abstract
Thyroid hormone is essential for normal metabolism and development, and overt abnormalities in thyroid function lead to common endocrine disorders affecting approximately 10% of individuals over their life span. In addition, even mild alterations in thyroid function are associated with weight changes, atrial fibrillation, osteoporosis, and psychiatric disorders. To identify novel variants underlying thyroid function, we performed a large meta-analysis of genome-wide association studies for serum levels of the highly heritable thyroid function markers TSH and FT4, in up to 26,420 and 17,520 euthyroid subjects, respectively. Here we report 26 independent associations, including several novel loci for TSH (PDE10A, VEGFA, IGFBP5, NFIA, SOX9, PRDM11, FGF7, INSR, ABO, MIR1179, NRG1, MBIP, ITPK1, SASH1, GLIS3) and FT4 (LHX3, FOXE1, AADAT, NETO1/FBXO15, LPCAT2/CAPNS2). Notably, only limited overlap was detected between TSH and FT4 associated signals, in spite of the feedback regulation of their circulating levels by the hypothalamic-pituitary-thyroid axis. Five of the reported loci (PDE8B, PDE10A, MAF/LOC440389, NETO1/FBXO15, and LPCAT2/CAPNS2) show strong gender-specific differences, which offer clues for the known sexual dimorphism in thyroid function and related pathologies. Importantly, the TSH-associated loci contribute not only to variation within the normal range, but also to TSH values outside the reference range, suggesting that they may be involved in thyroid dysfunction. Overall, our findings explain, respectively, 5.64% and 2.30% of total TSH and FT4 trait variance, and they improve the current knowledge of the regulation of hypothalamic-pituitary-thyroid axis function and the consequences of genetic variation for hypo- or hyperthyroidism.
Description
Keywords
Genome wide Association , Factor binding protein 5 , Hormone pathway genes , Serum TSH , Common variation , Cleft palate , Expression , Growth , Hypothyroidism , Thyrotropin
Citation
Porcu E, Medici M, Pistis G, Volpato CB, Wilson SG, Cappola AR, et al. (2013) A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function. PLoS Genet 9(2): e1003266. doi:10.1371/journal.pgen.1003266
Link to publisher’s version