Familial longevity is associated with lower baseline bone turnover but not differences in bone turnover in response to rhTSH.

INTRODUCTION

Previous studies on the relationship between thyroid function disturbance and the development of gestational diabetes mellitus (GDM) have reported inconsistent results. We aimed to investigate the relationship between thyroid function disturbance and GDM using Mendelian randomization (MR) analysis.

MATERIAL AND

METHODS

This MR study used summary data from genome-wide association studies (GWAS) of thyroid function disturbance (18,297 individuals) and GDM (41,647 participants). The inverse variance weighted (IVW) method was primarily employed for analysis, complemented by the weighted median, weighted mode, and MR-Egger regression. Sensitivity analyses included MR-Egger, MR-PRESSO, Cochran's Q, and leave-one-out approaches to assess the robustness of the findings.

RESULTS

The genetically determined thyroid function disturbance did not exhibit a statistically significant causal effect on GDM (FT4: OR = 0.99, 95% CI: 0.88-1.11, p = 0.84; TT3: OR = 1.10, 95% CI: 0.98-1.24, p = 0.12; FT3: OR = 1.16, 95% CI: 0.96-1.40, p = 0.13; TSH: OR = 1.01, 95% CI: 0.94-1.08, p = 0.83; FT3/FT4: OR = 1.05, 95% CI: 0.58-1.91, p = 0.87). The sensitivity analysis revealed no significant horizontal pleiotropy and identified outliers that, once excluded, did not alter the negative findings, confirming the robustness of the outcomes.

CONCLUSIONS

Our study found no significant causal effect of thyroid function disturbance on the risk of GDM based on the MR analysis, highlighting the need for further research to explore alternative mechanisms or potential subgroups where thyroid function may play a role in GDM development.