Arrhythmias & electrophysiology

Sodium–glucose co-transporter-2 inhibitors for the prevention of atrial fibrillation: a systemic review and meta-analysis

Eur J Prev CardiolPublished Systematic review and meta-analysis of randomised trials

Pooled result · AF occurrenceResult — go to the resultRelative risk 0.90 95% CI 0.80–1.01

Authors' conclusion

For patients with cardiometabolic diseases or risk factors, SGLT2 inhibitors did not decrease the risk of AF occurrence, regardless of follow-up duration, type or dose of the drug, or the patient population.

Study context

Population
Patients with DM, HF, CKD or cardiometabolic risk factors
Participants
101,100 patients46 RCTs
Comparison
SGLT2 inhibitors vs placebo
Outcome
AF occurrence
Methodological detailsplacebo-controlled trials
  • Placebo-controlled trials

Pooled result

As reported in the abstract

Relative risk

0.90

95% CI 0.80–1.01

SGLT2 inhibitors vs Placebo
RR 0.90 (95% CI 0.80–1.01)

Further pooled results

OutcomeRR (95% CI)
AF occurrence, by SGLT2 inhibitorCanagliflozin vs Placebo0.82 (0.60–1.12)
AF occurrence, by SGLT2 inhibitorDapagliflozin vs Placebo0.87 (0.73–1.03)
AF occurrence, by SGLT2 inhibitorEmpagliflozin vs Placebo0.97 (0.78–1.22)
AF occurrence, by SGLT2 inhibitorSotagliflozin vs Placebo0.99 (0.66–1.50)
AF occurrence, by SGLT2 inhibitorErtugliflozin vs Placebo0.87 (0.58–1.29)

Atrial fibrillation (AF) occurrence, by dose and in DM, HF and CKD subgroups

Similar results across doses; no association in patients with DM, HF or CKD

Original publication

Sodium–glucose co-transporter-2 inhibitors for the prevention of atrial fibrillation: a systemic review and meta-analysis. Eur J Prev Cardiol. Published 15 November 2023. doi:10.1093/eurjpc/zwad356

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