Causal relationship between type 1 diabetes and hypothyroidism: A Mendelian randomization study

Clin Endocrinol (Oxf). 2022 Dec;97(6):740-746. doi: 10.1111/cen.14801. Epub 2022 Sep 7.

Abstract

Objectives: Although an association between type 1 diabetes (T1D) and hypothyroidism has been found in multiple observational studies, whether T1D plays a causal role in the development of hypothyroidism remains uncertain. Therefore, this Mendelian randomization (MR) study aimed to investigate the causal association between T1D and hypothyroidism.

Methods: Independent single-nucleotide polymorphisms associated with T1D with genome-wide significance were selected as instrumental variables from a large genome-wide association study (GWAS) of T1D. Hypothyroidism GWAS summary statistics were obtained from the Thyroidomics Consortium. The inverse-variance weighted (IVW) method was used as the primary analysis for estimating the effect of the exposure on the outcome. We also used MR-Egger, the weighted median method, MR-Robust, and other methods to confirm the results.

Results: T1D had a positive causal association with hypothyroidism [IVW, odds ratio (OR) = 1.083, 95% confidence interval (CI), 1.046-1.122; p < .001]. MR-Egger regression indicated that directional pleiotropy did not bias the result (intercept = 0.006; p = .295). The causal association was verified in an independent validation set (IVW, OR = 1.099, 95% CI, 1.018-1.186; p = .017). The results were robust according to various MR methods, and the results of the reverse MR analysis did not support reverse causation (p > .05).

Conclusions: The MR analysis results indicated a causal association between T1D and hypothyroidism. Therefore, it is recommended that patients with T1D undergo thyroid function tests regularly to minimize the risk of undiagnosed hypothyroidism among young patients with T1D.

Keywords: Mendelian randomization; hypothyroidism; type 1 diabetes.

MeSH terms

  • Diabetes Mellitus, Type 1* / genetics
  • Genome-Wide Association Study
  • Humans
  • Hypothyroidism* / genetics
  • Mendelian Randomization Analysis
  • Polymorphism, Single Nucleotide / genetics