Cardiometabolic & kidney

Cardiovascular outcomes and safety of semaglutide in non-overweight populations with type 2 diabetes: a comparison with dipeptidyl peptidase 4 inhibitors

Eur Heart J Qual Care Clin OutcomesPublished Retrospective cohort study

Main finding · All-cause mortalityResult — go to the resultHazard ratio 0.54 95% CI 0.45–0.65

Authors' conclusion

In patients with T2D and BMI <25 kg/m2, semaglutide was associated with a lower 3-year risk of all-cause mortality than DPP-4 inhibitors.

Study context

Population
Patients with T2DM and body mass index (BMI) <25 kg/m², TriNetX electronic medical records, 2018–20204,194 per group after matching
Participants
340,721 patients
Exposure
Semaglutide vs DPP-4 inhibitors
  • Semaglutiden = 4,194
  • DPP-4 inhibitorn = 4,194reference
Outcome
Cumulative incidence of all-cause mortality
Follow-up
3 years
Methodological detailspropensity-score matched
  • Propensity-score matched

Main finding

All-cause mortality

Hazard ratio

0.54

95% CI 0.45–0.65

P < 0.001

By group

Semaglutidevs DPP-4 inhibitor
HR 0.54 (95% CI 0.45–0.65); P < 0.001

As reported in the abstract

Observational data: associations, not effects.

Secondary outcomes

OutcomeSemaglutideHR (95% CI)P value
Acute MI · 3 yearsSemaglutidevs DPP-4 inhibitorsPropensity score matching0.87 (0.72–1.06)P = 0.173
Stroke · 3 yearsSemaglutidevs DPP-4 inhibitorsPropensity score matching8.4%1.11 (0.94–1.32)P = 0.220
  • Stroke: DPP-4 inhibitors 7.7%

Safety

Nausea and vomiting, diarrhoea, hypoglycaemia

Not significantly different between the groups

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Cardiovascular outcomes and safety of semaglutide in non-overweight populations with type 2 diabetes: a comparison with dipeptidyl peptidase 4 inhibitors. Eur Heart J Qual Care Clin Outcomes. Published 17 July 2025. doi:10.1093/ehjqcco/qcaf065

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