Lupus & antiphospholipid syndrome

Cardiovascular outcomes and safety of SGLT2 inhibitors in rheumatic diseases: a systematic review of evidence predominantly from systemic lupus erythematosus and systemic sclerosis

Semin Arthritis RheumPublished systematic review

Authors' conclusion

Predominantly observational data suggest a potential cardiovascular benefit of SGLT2 inhibitors in rheumatic IMIDs, but the available evidence is confined largely to SLE and SSc populations. Whilst SGLT2 inhibitors should be used in established indications of type 2 diabetes mellitus, heart failure and chronic kidney disease, prospective and controlled studies in IMID populations are needed to establish their cardiovascular benefit, clarify safety and evaluate for effect on disease activity.

Study context

Population
Adults with rheumatic immune-mediated inflammatory diseases (IMIDs) using SGLT2i, predominantly systemic lupus erythematosus and systemic sclerosisIMID participants in five studies, systemic sclerosis (SSc) 25.4%, systemic lupus erythematosus (SLE) 70.9%, other IMIDs 3.9%
Participants
11,190 adults
Comparison
SGLT2i use in IMID patients
Outcome
All-cause mortality and heart failure risk (three studies reporting major adverse cardiovascular events (MACE))
Methodological detailsFollowing PRISMA guidance, observational and interventional adult IMID studies
  • Following PRISMA guidance
  • Observational and interventional adult IMID studies

Pooled result

As reported in the abstract

  • SGLT2i use was associated with lower all-cause mortality and heart failure risk

Further pooled results

Myocardial infarction

No clear effect on myocardial infarction

Hospitalisation, treatment discontinuation and IMID flare

Evidence limited and inconsistent

Original publication

Cardiovascular outcomes and safety of SGLT2 inhibitors in rheumatic diseases: a systematic review of evidence predominantly from systemic lupus erythematosus and systemic sclerosis. Semin Arthritis Rheum. Published 22 October 2026. doi:10.1016/j.semarthrit.2026.153090

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