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J Parathyr Dis. 2025;13: e13293.
doi: 10.34172/jpd.2025.13293
  Abstract View: 89
  PDF Download: 83

Meta-analysis

Association between glucagon-like peptide-1 receptor agonists and thyroid carcinoma; a systematic review and meta-analysis of observational studies

Mojtaba Lotfi 1 ORCID logo, Mahboobeh Akhondi 2 ORCID logo, Mehrangiz Ghafari 3 ORCID logo, Mahmoud Dehghani-ghorbi 4 ORCID logo, Mehrnaz Nazari Rad 5 ORCID logo, Maedeh Seifollahi Marbini 6 ORCID logo, Mahsa Ebrahimi 7 ORCID logo, Seyed Amir Sheikholeslami 8 ORCID logo, Sajad Ataei Azimi 9* ORCID logo

1 Clinical Research Development Unit of Akbar Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
2 Department of Anesthesiology, School of Medicine, Ali Ibn Abitaleb Educational and Treatment Hospital, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
3 Department of Pathology, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran.
4 Hematology-Oncology Department, Imam Hossein Educational Hospital, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
5 Clinical Research Development Unit of Akbar Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
6 School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
7 Department of Clinical Oncology, Imam Hossein Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
8 Department of Hematology-Oncology, Imam Hossein Hospital, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
9 Hematology-Oncology Department, Mashhad University of Medical Sciences, Mashhad, Iran.
*Corresponding Author: Sajad Ataei Azimi, Email: ataeiazimis@mums.ac.ir

Abstract

Introduction: Glucagon-like peptide-1 receptor agonists (GLP1-RAs) are drugs administered to treat type 2 diabetes mellitus; however, their relationship with thyroid cancer is still unclear. Hence, the present study aimed to examine the association between the use of GLP1-RA and thyroid carcinoma.

Materials and Methods: Databases searched—including Web of Science, Cochrane, Scopus, ProQuest, PubMed, Embase, and Google Scholar—were searched without a time limit until May 1, 2025. Data were entered into SPSS 19 and analyzed using STATA 14. Tests with P values less than 0.05 were considered statistically significant (P < 0.05).

Results: The relationship between GLP1-RA and thyroid carcinoma based on hazard ratio (HR: 1.14, 95% CI: 0.86, 1.51) and incidence rate ratio (IRR: 1.32, 95% CI: 0.79, 2.20) was statistically insignificant. However, according to odds ratio (OR), use of GLP1-RA increased the risk of thyroid cancer (OR: 1.46, 95% CI: 1.23, 1.74). Furthermore, the association between GLP1-RA and medullary thyroid carcinoma was insignificant (HR: 1.51, 95% CI: 0.90, 2.54). The relationship between GLP1-RA and thyroid carcinoma among women (HR: 1.01, 95% CI: 0.69, 1.47), men (HR: 0.72, 95% CI: 0.33, 1.57), individuals aged 50 to 59 (HR: 1.30, 95% CI: 0.96, 1.75), 60 to 69 (HR: 0.95, 95% CI: 0.65, 1.38), in China (HR: 1.26, 95% CI: 0.91, 1.76), France (HR: 3.43, 95% CI: 1.30, 9.04), and Korea (HR: 1.05, 95% CI: 0.76, 1.46) was statistically insignificant. However, in the USA (HR: 1.44, 95% CI: 1.22, 1.71), GLP1-RA administration increased the risk of thyroid neoplasm.

Conclusion: Generally, the relationship between the GLP1-RA use in patients with type 2 diabetes mellitus and the risk of thyroid carcinoma was insignificant.

Registration: This study has been compiled based on the PRISMA checklist, and its protocol was registered on the PROSPERO (ID: CRD420251051827) and Research Registry (reviewregistry1993) websites.



Please cite this paper as: Lotfi M, Akhondi M, Ghafari M, Dehghani-ghorbi M, Nazari Rad M, Seifollahi Marbini M, Ebrahimi M, Sheikholeslami SA, Ataei Azimi S. Association between glucagon-like peptide-1 receptor agonists and thyroid carcinoma; a systematic review and meta-analysis of observational studies. J Parathyr Dis. 2025;13:e13293. doi:10.34172/jpd.2025.13293.
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Submitted: 14 Mar 2025
Revision: 18 May 2025
Accepted: 27 May 2025
ePublished: 01 Jun 2025
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