Effects of SGLT2i therapy on cardiac electrophysiological properties and arrhythmias in diabetic patients with implantable cardiac defibrillator
Sodium-glucose-transporter-2-inhibitors (SGLT2i) reduce ventricular-tachycardia (VT) and cardiac deaths in diabetic patients with internal-cardioverter-defibrillators (ICD) and/or cardiac-resynchronization-therapy (CRT). SGLT2i might improve cardiac electrophysiological-properties, reducing inflammation and sympathetic tone. We evaluated SGLT2i effects on lead-parameters, arrhythmias, ICDs' interventions, and heart failure (HF) hospitalizations and cardiac deaths in diabetics at 1 year of follow-up. At 1 year of follow-up, 334 SGLT2i-users vs. 794 non-users patients had lower heart rate, best clinical status, lowest B-type-natriuretic-peptide (BNP) and N-terminal pro-BNP, and inflammatory markers and catecholamines (p < 0.05). SGLT2i-users vs. non-users showed cardiac remodeling and increased cardiac pump (p < 0.05), significant reduction of right-ventricle (RV) and left-ventricle (LV) pacing, increase of RV/LV impedance and sensing at follow-up end (p < 0.05). C-reactive-protein (CRP) inversely linked to RV sensing and linearly to RV pacing. CRP and tumor-necrosis-alpha (TNFa) inversely linked to RV and shock impedance (p < 0.05). At follow-up end, SGLT2i-users vs. non-users showed lower rate of VT (36 (10.8 %) vs. 138 (17.4 %)), inappropriate-shocks (32 (9.6 %) vs. 118 (14.9 %)), HF hospitalizations (50 (15.0 %) vs. 216 (27.2 %)), and cardiac deaths (10 (3.0 %) vs. 53 (6.7 %)), (p < 0.05). BNP (HR 1.101, CI 95 % 1.000-1.305), CRP (HR 1.034, CI 95 % 1.007-1.061), and SGLT2i (HR 0.592, CI 95 % 0.410-0.854) predicted VT; SGLT2i (HR 0.611, CI 95 % 0.413-0.903) predicted inappropriate-shocks; BNP (HR 1.012, CI 95 % 1.001-1.040) predicted appropriate-shocks. CRP (HR 1.102, 1.077-1.127), ischemic cardiomyopathy (HR 1.284, CI 95 % 1.14-1.870), and SGLT2i (HR 0.497, CI 95 % 0.365-0.677) predicted HF-hospitalizations. SGLT2i (HR 0.677, CI 95 % 0.222-0.860) predicted cardiac deaths. SGLT2i improve electrophysiological-properties and reduce arrhythmias in diabetics with ICD/CRT.
Authors
- Paolo Calabrò (ORCID: https://orcid.org/0000-0002-5018-830X)
- C. La Marca
- Fabrizio Turriziani
- Annalisa Capuano (ORCID: https://orcid.org/0000-0002-8653-2408)
- Concetta Rafaniello (ORCID: https://orcid.org/0000-0002-7107-4280)
- Carmine Pizzi (ORCID: https://orcid.org/0000-0002-4048-675X)
- Raffaele Marfella (ORCID: https://orcid.org/0000-0003-3960-9270)
- Ludovica Vittoria Marfella
- Ciro Mauro (ORCID: https://orcid.org/0000-0003-3611-2330)
- Matteo Santamaria (ORCID: https://orcid.org/0000-0003-1000-0592)
- Ferdinando Carlo Sasso (ORCID: https://orcid.org/0000-0002-9142-7848)
- Maria Consiglia Trotta (ORCID: https://orcid.org/0000-0001-9813-5955)
- Giuseppe Paolisso (ORCID: https://orcid.org/0000-0002-2137-455X)
- Giovambattista D'Amico
- Celestino Sardu (ORCID: https://orcid.org/0000-0001-5099-3790)
- Valerio Giordano
Institutions
- University of Campania "Luigi Vanvitelli" (IT)
- Santa Maria Nuova Hospital (IT)
- Hospital Episcopal San Lucas (PR)
- Ospedale Antonio Cardarelli (IT)
- Ospedale Santa Maria (IT)
- Azienda USL di Bologna (IT)
- University of Campania "Luigi Vanvitelli" (IT)
Publication Details
- Journal
- Pharmacological Research
- Published
- 2025-05-04
- DOI
- https://doi.org/10.1016/j.phrs.2025.107759
- Citations
- 9
- Primary Topic
- Cardiovascular Function and Risk Factors
- Type
- article
- Field-Weighted Citation Impact
- 12.49