Evidence mapPaperPMID 40201679Full record

ArticleHeart rhythm O22025

Sodium-glucose cotransporter-2 inhibitor use in type 2 diabetes mellitus is associated with a lower rate of atrial arrhythmias in a hospitalized real-world population.

Kathryn D Tiver, Derek P Chew, Jia Y Tan, Kristina Lambrakis, Carmine G De Pasquale, Anand N Ganesan

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Article in Heart rhythm O2, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Kathryn D TiverCollege of Medicine and Public Health, Flinders University, South Australia, Australia.
Derek P ChewCollege of Medicine and Public Health, Flinders University, South Australia, Australia.
Jia Y TanCollege of Medicine and Public Health, Flinders University, South Australia, Australia.
Kristina LambrakisCollege of Medicine and Public Health, Flinders University, South Australia, Australia.
Carmine G De PasqualeCollege of Medicine and Public Health, Flinders University, South Australia, Australia.
Anand N GanesanCollege of Medicine and Public Health, Flinders University, South Australia, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sodium-glucose cotransporter-2 inhibitors (SGLT2is) have been associated with lower rates of cardiac arrhythmias in Objective: The purpose of this study was to determine the effects of SGLT2i on cardiac arrhythmias in a real-world, hospitalized population. Methods: A retrospective cohort study was performed in South Australia, Australia. Patients (n = 882) with type 2 diabetes mellitus (T2DM) on oral diabetic therapy (33.6% females, median age 62.3 years) who received SGLT2i (for T2DM) were identified through public hospital admissions from 2011-2019. Patients were matched with 3282 contemporaneous controls with T2DM who did not receive SGLT2i. Baseline characteristics were adjusted using inverse probability treatment weighting. The primary outcome was incidence of atrial arrhythmias. Secondary outcomes included incidence of ventricular arrhythmias and cardiac arrest at 2 years. Results: All-cause mortality was higher in the SGLT2i group (hazard ratio [HR] 2.02, 95% confidence interval [CI] 1.55-2.63, Conclusion: In this real-world, comorbid inpatient cohort, SGLT2i treatment was associated with a lower incidence of atrial arrhythmias. Prospective randomized trials evaluating SGLT2i as specific atrial fibrillation pharmacotherapy are underway.

Indexed as

Atrial fibrillationCardiac arrhythmiasObservational studySGLT2iSodium-glucose cotransporter-2 inhibitor

Identifiers

PMID40201679
PMCPMC11973685

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.