Complex Interactions Between Abnormal Thyroid Function and Neurodevelopmental Disorders: A Mendelian Randomization Study
Background Neurodevelopmental disorders (NDDs), such as attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and tic disorders (TD), have been frequently investigated due to their profound impacts on social and emotional functions. In this regard, there is a new focus on the possible association between these disorders and thyroid dysfunction. The purpose of this study is to explore the relationship between NDDs and hyperthyroidism and hypothyroidism. Methods In this study, we used MR analysis to explore the associations of ADHD, ASD and TD with hyperthyroidism and hypothyroidism. MR analysis explores the associations between exposure and outcome using Mendelian randomization framework, and is based on extensive genomic data sets. Results Our results suggested that hypothyroidism was associated with TD, while no individual genetic variant was associated with hypothyroidism, ADHD, or ASD. Additionally, we found no reliable evidence that ADHD, ASD, or TD were causally linked to hyperthyroidism. There was also no credible evidence that any individual genetic variant was associated with an increased risk of hyperthyroidism. Our findings remained robust in sensitivity analyses. Conclusion Our study provides new insights into the relationship between NDDs and thyroid dysfunction. It suggests that there were potential risk factors and causal pathways, and calls for early diagnosis, intervention, and integrated health care.
Authors
- Zhiguo Ding (ORCID: https://orcid.org/0000-0001-5280-384X)
- Jingwei Zhou (ORCID: https://orcid.org/0009-0003-1617-9447)
- Han Bai
- Zhe Li (ORCID: https://orcid.org/0009-0008-9803-7608)
- Junhui Wang
- Xin'ai Li
- Xiaoheng Chen
- Ping Pan
Publication Details
- Journal
- Neuroendocrinology
- Published
- 2026-07-16
- DOI
- https://doi.org/10.1159/000553604
- Primary Topic
- Thyroid Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00