ArticleCureus2025
Dual Glucagon-Like Peptide-1 (GLP-1) and Glucose-Dependent Insulinotropic Polypeptide (GIP) Receptor Agonist-Associated Thyroiditis: A Case Report of Thyroid Dysfunction Following Tirzepatide Use.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Article
- Delayed-Onset Amiodarone Induced Thyrotoxicosis After Glucagon-Like Peptide-1 Agonist-Related Weight Loss.JCEM case reports · 2026Article
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Drug-induced thyroiditis is an uncommon but clinically important condition. As dual glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) receptor agonists like tirzepatide are increasingly used for weight management and blood sugar control, there is growing interest in understanding their potential thyroid-related effects. We report a 32-year-old woman with no personal or family history of thyroid disease who developed painless biphasic thyroiditis, initial thyrotoxicosis followed by transient hypothyroidism, after two months of tirzepatide therapy. Thyroid autoantibodies were negative, and ultrasound showed heterogeneous echotexture with increased vascularity, consistent with thyroiditis. Infectious, autoimmune, postpartum, and infiltrative causes were excluded based on clinical history, laboratory findings, and imaging. Thyroid function normalized two months after discontinuing tirzepatide without the need for treatment. This case highlights a possible association between tirzepatide and drug-induced painless thyroiditis. It adds to the limited literature and emphasizes the need for clinician awareness of this possible adverse effect.
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Registered trials
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