Endocrine oncology

Glucagon-like peptide 1 receptor agonist use and risk of thyroid cancer: Scandinavian cohort study

BMJPublished Cohort study

Authors' conclusion

In this large cohort study using nationwide data from three countries, GLP1 receptor agonist use was not associated with a substantially increased risk of thyroid cancer over a mean follow-up of 3.9 years. In the main analysis comparing GLP1 receptor agonists with DPP4 inhibitors, the upper limit of the confidence interval was consistent with no more than a 31% increase in relative risk.

Study context

Population
New users of GLP-1 RA or DPP-4i (additional analysis: SGLT2i), Denmark, Norway and Sweden, 2007–21
Exposure
GLP-1 RA vs DPP-4i
  • GLP1 receptor agonistn = 145,410
  • DPP4 inhibitorn = 291,667reference
Outcome
Thyroid cancer identified from nationwide cancer registers
Methodological detailsactive-comparator new user design, propensity score weighting, nationwide registers, multinational (Denmark, Norway, Sweden)
  • Active-comparator new user design
  • Propensity score weighting
  • Nationwide registers
  • Multinational (Denmark, Norway, Sweden)

Main finding

As reported in the abstract

Thyroid cancer · mean follow-up 3.9 years (GLP-1 RA) and 5.4 years (DPP-4i)

GLP-1 RA

1.33 events per 10 000 person years

76 events

DPP-4i

1.46 events per 10 000 person years

184 events

Hazard ratio (95% CI)
GLP-1 RAvs DPP-4i
0.93(0.66–1.31)
Rate difference, events per 10 000 person years (95% CI)
GLP-1 RAvs DPP-4i
−0.13(−0.61 to 0.36)

Observational data: associations, not effects.

Further findings

OutcomeHR (CI)
Medullary thyroid cancerGLP-1 RAvs DPP-4i1.19 (0.37–3.86)
Thyroid cancer, additional analysisvs SGLT2i1.16 (0.65–2.05)

Original publication

Glucagon-like peptide 1 receptor agonist use and risk of thyroid cancer: Scandinavian cohort study. BMJ. Published 10 April 2024. doi:10.1136/bmj-2023-078225

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