Type 2 & other diabetes

Effect of empagliflozin on total myocardial infarction events by type and additional coronary outcomes: insights from the randomized EMPA-REG OUTCOME trial

Cardiovasc DiabetolPublished Secondary analysis of the EMPA-REG OUTCOME randomised trial

Primary result · Total MI eventsResult — go to the resultRate ratio 0.79 95% CI 0.620–0.998

Authors' conclusion

In T2D patients with ASCVD, empagliflozin reduced the risk of MIs, with consistent effects across the two most common etiologies, i.e. type 1 and 2.

Study context

Population
People with T2D and CVD (mostly atherosclerotic)
Participants
7,020 people
Comparison
Empagliflozin vs placebo
Primary endpoint
Total (first plus recurrent) centrally adjudicated fatal and non-fatal MI events
Follow-up
Median 3.1 years
Methodological detailsprespecified and post-hoc analyses
  • Prespecified and post-hoc analyses

Primary result

Total MI events

Rate ratio

0.79

95% CI 0.620–0.998

P = 0.0486

Empagliflozinvs Placebo
rate ratio 0.79 (95% CI 0.620–0.998); P = 0.0486

As reported in the abstract

Total myocardial infarction (MIs) (including recurrent)
421
Risk of total MI events reduced with empagliflozin
21%

Further findings

OutcomeRate ratio (95% CI)
Type 1 MI (post hoc)0.79 (0.61–1.04)
Type 2 MI (post hoc)0.67 (0.41–1.10)
Type 1 MI (post hoc) — Type 1 events
299
Type 2 MI (post hoc) — Type 2 events
86

Type 3, 4 and 5 MI events (post hoc)

Type 3 events
26
Type 4 events
19
Type 5 events
1
  • MIs could be assigned to > 1 type

Original publication

Effect of empagliflozin on total myocardial infarction events by type and additional coronary outcomes: insights from the randomized EMPA-REG OUTCOME trial. Cardiovasc Diabetol. Published 11 July 2024. doi:10.1186/s12933-024-02328-6

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