4.7 Article

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With KLF9 and DOT1L

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 106, Issue 5, Pages E2191-E2202

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgaa975

Keywords

epigenetics; EWAS; thyroid hormone; DNA methylation; KLF9; DOT1L

Funding

  1. Australian National Health and Medical Research Council (NHMRC) [1087407]
  2. NHMRC [1031119, 1010374, 496667, 1046880, 1059711, 353514, 403981, 14254]
  3. National Institutes of Health (NIH) [GM057091, GM099568]
  4. Australian Research Council [A7960034, A79906588, A79801419, DP0212016, DP0343921, DP1093900]
  5. NHMRC Medical Bioinformatics Genomics Proteomics Program [389891]
  6. Sir Charles Gairdner Osborne Park Health Care Group Research Advisory Committee [2018-19/015]
  7. iVEC/Pawsey Supercomputing Centre
  8. Australian Government
  9. Government of Western Australia [Pawsey0260, Director2025]
  10. National Health and Medical Research Council of Australia [1087407, 1059711] Funding Source: NHMRC

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This study identified associations between blood-based DNAm and both fT3 and TSH, shedding light on the mechanisms underlying thyroid hormone action and/or pituitary-thyroid axis function.
Context: Circulating concentrations of free triiodothyronine (fT3), free thyroxine (fT4), and thyrotropin (TSH) are partly heritable traits. Recent studies have advanced knowledge of their genetic architecture. Epigenetic modifications, such as DNA methylation (DNAm), may be important in pituitary-thyroid axis regulation and action, but data are limited. Objective: To identify novel associations between fT3, fT4, and TSH and differentially methylated positions (DMPs) in the genome in subjects from 2 Australian cohorts. Method: We performed an epigenome-wide association study (EWAS) of thyroid function parameters and DNAm using participants from: Brisbane Systems Genetics Study (median age 14.2 years, n = 563) and the Raine Study (median age 17.0 years, n = 863). Plasma fT3, fT4, and TSH were measured by immunoassay. DNAm levels in blood were assessed using Illumina HumanMethylation450 BeadChip arrays. Analyses employed generalized linear mixed models to test association between DNAm and thyroid function parameters. Data from the 2 cohorts were meta-analyzed. Results: We identified 2 DMPs with epigenome-wide significant (P < 2.4E-7) associations with TSH and 6 with fT3, including cg00049440 in KLF9 (P = 2.88E-10) and cg04173586 in DOT1L (P = 2.09E-16), both genes known to be induced by fT3. All DMPs had a positive association between DNAm and TSH and a negative association between DNAm and fT3. There were no DMPs significantly associated with fT4. We identified 23 differentially methylated regions associated with fT3, fT4, or TSH. Conclusions: This study has demonstrated associations between blood-based DNAm and both fT3 and TSH. This may provide insight into mechanisms underlying thyroid hormone action and/or pituitary-thyroid axis function.

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