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Implications of Glucagon-like Peptide-1 Receptor Agonists on Thyroid Function and Thyroid Nodules: A Drug Target
Zhijun Zhang1, Jingyun Yang1, Ling Gao1
1Department of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, China.
Objectives:
Glucagon-like Peptide-1 receptor agonists (GLP-1RAs) are antidiabetic medications, with conflicting reports about their relationship with thyroid diseases. This study investigates their effects on thyroid function and nodules in patients with diabetes.
Methods:
Mendelian randomization was conducted to examine the association between genetically proxied GLP-1RA activity and thyroid diseases. This was followed by a cohort study involving 169 patients with diabetes, who were divided into a control group (control group, W/O GLP-1 treatment) and a GLP-1RA treatment group (GLP-1RAs group) based on their medication usage. Patients' thyroid function tests, thyroid nodule diameters, and Thyroid Imaging Reporting and Data System classifications were compared at baseline and after 12 months of treatment.
Results:
Through Mendelian randomization, GLP-1RAs decrease free thyroxine (fT4) levels within the normal range [odds ratio (95% CI) = 0.9948 (0.9936-0.9961), P < .001]. Cohort study showed that after treatment, the nodule diameter increased in both the control group (0.69 vs 0.77, P = .004) and the GLP-1 group (0.68 vs 0.71, P = .019). In the GLP-1 group, the Thyroid Imaging Reporting and Data System (2.60 vs 2.69, P = .007) levels increased, while the fT4 (1.26 vs 1.17, P = .005) levels decreased. However, linear regression did not show significant association between GLP-1 and post-treatment differences in thyroid function or thyroid nodule.
Conclusions:
GLP-1RAs treatment of 12 months in patients with diabetes is considered relatively safe regarding thyroid disease although there is a potential risk for decreasing of fT4 levels and nodule growth/progression, with no clear evidence of superiority over other antidiabetic treatments.
Insights
Glucagon-like peptide-1 (GLP-1) receptor agonists may decrease free thyroxine (fT4) levels and potentially increase thyroid nodule size in diabetic patients. While generally safe for thyroid health, these effects warrant monitoring during treatment.
Area of Science:
- Endocrinology
- Pharmacology
- Diabetology
Background:
- Glucagon-like peptide-1 (GLP-1) receptor agonists are widely used for type 2 diabetes management.
- Conflicting evidence exists regarding their impact on thyroid function and nodule development.
- This study aims to clarify the relationship between GLP-1 receptor agonists and thyroid health in diabetic individuals.
Purpose of the Study:
- To investigate the effects of GLP-1 receptor agonists on thyroid function and nodule progression in patients with diabetes.
- To assess the safety profile of GLP-1 receptor agonists concerning thyroid diseases.
Main Methods:
- A Mendelian randomization study was performed to analyze the genetic association between GLP-1 receptor agonist activity and thyroid diseases.
- A cohort study compared 169 diabetic patients (control vs. GLP-1 receptor agonist treatment group) over 12 months.
- Thyroid function tests, nodule diameters, and TI-RADS classifications were evaluated at baseline and after treatment.
Main Results:
- Mendelian randomization indicated that GLP-1 receptor agonists decrease free thyroxine (fT4) levels within the normal range.
- The cohort study observed increased nodule diameter in both control and GLP-1 receptor agonist groups after 12 months.
- In the GLP-1 receptor agonist group, TI-RADS levels increased, and fT4 levels decreased significantly.
Conclusions:
- Twelve-month treatment with GLP-1 receptor agonists appears relatively safe for thyroid health in diabetic patients.
- Potential risks include a decrease in fT4 levels and possible nodule growth or progression.
- No clear evidence suggests superiority over other antidiabetic treatments regarding thyroid outcomes.
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