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In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study

BACKGROUND: Sodium-glucose co-transporter 2 inhibitors (SGLT2-i) have shown significant cardiovascular benefits in patients with and without type 2 diabetes mellitus (T2DM). They have also gained interest for their potential anti-arrhythmic role and their ability to reduce the occurrence of atrial f...

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Autores principales: Cesaro, Arturo, Gragnano, Felice, Paolisso, Pasquale, Bergamaschi, Luca, Gallinoro, Emanuele, Sardu, Celestino, Mileva, Niya, Foà, Alberto, Armillotta, Matteo, Sansonetti, Angelo, Amicone, Sara, Impellizzeri, Andrea, Esposito, Giuseppe, Morici, Nuccia, Oreglia, Jacopo Andrea, Casella, Gianni, Mauro, Ciro, Vassilev, Dobrin, Galie, Nazzareno, Santulli, Gaetano, Pizzi, Carmine, Barbato, Emanuele, Calabrò, Paolo, Marfella, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551177/
https://www.ncbi.nlm.nih.gov/pubmed/36237914
http://dx.doi.org/10.3389/fcvm.2022.1012220
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author Cesaro, Arturo
Gragnano, Felice
Paolisso, Pasquale
Bergamaschi, Luca
Gallinoro, Emanuele
Sardu, Celestino
Mileva, Niya
Foà, Alberto
Armillotta, Matteo
Sansonetti, Angelo
Amicone, Sara
Impellizzeri, Andrea
Esposito, Giuseppe
Morici, Nuccia
Oreglia, Jacopo Andrea
Casella, Gianni
Mauro, Ciro
Vassilev, Dobrin
Galie, Nazzareno
Santulli, Gaetano
Pizzi, Carmine
Barbato, Emanuele
Calabrò, Paolo
Marfella, Raffaele
author_facet Cesaro, Arturo
Gragnano, Felice
Paolisso, Pasquale
Bergamaschi, Luca
Gallinoro, Emanuele
Sardu, Celestino
Mileva, Niya
Foà, Alberto
Armillotta, Matteo
Sansonetti, Angelo
Amicone, Sara
Impellizzeri, Andrea
Esposito, Giuseppe
Morici, Nuccia
Oreglia, Jacopo Andrea
Casella, Gianni
Mauro, Ciro
Vassilev, Dobrin
Galie, Nazzareno
Santulli, Gaetano
Pizzi, Carmine
Barbato, Emanuele
Calabrò, Paolo
Marfella, Raffaele
author_sort Cesaro, Arturo
collection PubMed
description BACKGROUND: Sodium-glucose co-transporter 2 inhibitors (SGLT2-i) have shown significant cardiovascular benefits in patients with and without type 2 diabetes mellitus (T2DM). They have also gained interest for their potential anti-arrhythmic role and their ability to reduce the occurrence of atrial fibrillation (AF) and ventricular arrhythmias (VAs) in T2DM and heart failure patients. OBJECTIVES: To investigate in-hospital new-onset cardiac arrhythmias in a cohort of T2DM patients presenting with acute myocardial infarction (AMI) treated with SGLT2-i vs. other oral anti-diabetic agents (non-SGLT2-i users). METHODS: Patients from the SGLT2-I AMI PROTECT registry (NCT05261867) were stratified according to the use of SGLT2-i before admission for AMI, divided into SGLT2-i users vs. non-SGLT2-i users. In-hospital outcomes included the occurrence of in-hospital new-onset cardiac arrhythmias (NOCAs), defined as a composite of new-onset AF and sustained new-onset ventricular tachycardia (VT) and/or ventricular fibrillation (VF) during hospitalization. RESULTS: The study population comprised 646 AMI patients categorized into SGLT2-i users (111 patients) and non-SGLT2-i users (535 patients). SGLT2-i users had a lower rate of NOCAs compared with non-SGLT2-i users (6.3 vs. 15.7%, p = 0.010). Moreover, SGLT2-i was associated with a lower rate of AF and VT/VF considered individually (p = 0.032). In the multivariate logistic regression model, after adjusting for all confounding factors, the use of SGLT2-i was identified as an independent predictor of the lower occurrence of NOCAs (OR = 0.35; 95%CI 0.14–0.86; p = 0.022). At multinomial logistic regression, after adjusting for potential confounders, SGLT2-i therapy remained an independent predictor of VT/VF occurrence (OR = 0.20; 95%CI 0.04–0.97; p = 0.046) but not of AF occurrence. CONCLUSIONS: In T2DM patients, the use of SGLT2-i was associated with a lower risk of new-onset arrhythmic events during hospitalization for AMI. In particular, the primary effect was expressed in the reduction of VAs. These findings emphasize the cardioprotective effects of SGLT2-i in the setting of AMI beyond glycemic control. TRIAL REGISTRATION: Data are part of the observational international registry: SGLT2-I AMI PROTECT. ClinicalTrials.gov, identifier: NCT05261867.
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spelling pubmed-95511772022-10-12 In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study Cesaro, Arturo Gragnano, Felice Paolisso, Pasquale Bergamaschi, Luca Gallinoro, Emanuele Sardu, Celestino Mileva, Niya Foà, Alberto Armillotta, Matteo Sansonetti, Angelo Amicone, Sara Impellizzeri, Andrea Esposito, Giuseppe Morici, Nuccia Oreglia, Jacopo Andrea Casella, Gianni Mauro, Ciro Vassilev, Dobrin Galie, Nazzareno Santulli, Gaetano Pizzi, Carmine Barbato, Emanuele Calabrò, Paolo Marfella, Raffaele Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Sodium-glucose co-transporter 2 inhibitors (SGLT2-i) have shown significant cardiovascular benefits in patients with and without type 2 diabetes mellitus (T2DM). They have also gained interest for their potential anti-arrhythmic role and their ability to reduce the occurrence of atrial fibrillation (AF) and ventricular arrhythmias (VAs) in T2DM and heart failure patients. OBJECTIVES: To investigate in-hospital new-onset cardiac arrhythmias in a cohort of T2DM patients presenting with acute myocardial infarction (AMI) treated with SGLT2-i vs. other oral anti-diabetic agents (non-SGLT2-i users). METHODS: Patients from the SGLT2-I AMI PROTECT registry (NCT05261867) were stratified according to the use of SGLT2-i before admission for AMI, divided into SGLT2-i users vs. non-SGLT2-i users. In-hospital outcomes included the occurrence of in-hospital new-onset cardiac arrhythmias (NOCAs), defined as a composite of new-onset AF and sustained new-onset ventricular tachycardia (VT) and/or ventricular fibrillation (VF) during hospitalization. RESULTS: The study population comprised 646 AMI patients categorized into SGLT2-i users (111 patients) and non-SGLT2-i users (535 patients). SGLT2-i users had a lower rate of NOCAs compared with non-SGLT2-i users (6.3 vs. 15.7%, p = 0.010). Moreover, SGLT2-i was associated with a lower rate of AF and VT/VF considered individually (p = 0.032). In the multivariate logistic regression model, after adjusting for all confounding factors, the use of SGLT2-i was identified as an independent predictor of the lower occurrence of NOCAs (OR = 0.35; 95%CI 0.14–0.86; p = 0.022). At multinomial logistic regression, after adjusting for potential confounders, SGLT2-i therapy remained an independent predictor of VT/VF occurrence (OR = 0.20; 95%CI 0.04–0.97; p = 0.046) but not of AF occurrence. CONCLUSIONS: In T2DM patients, the use of SGLT2-i was associated with a lower risk of new-onset arrhythmic events during hospitalization for AMI. In particular, the primary effect was expressed in the reduction of VAs. These findings emphasize the cardioprotective effects of SGLT2-i in the setting of AMI beyond glycemic control. TRIAL REGISTRATION: Data are part of the observational international registry: SGLT2-I AMI PROTECT. ClinicalTrials.gov, identifier: NCT05261867. Frontiers Media S.A. 2022-09-27 /pmc/articles/PMC9551177/ /pubmed/36237914 http://dx.doi.org/10.3389/fcvm.2022.1012220 Text en Copyright © 2022 Cesaro, Gragnano, Paolisso, Bergamaschi, Gallinoro, Sardu, Mileva, Foà, Armillotta, Sansonetti, Amicone, Impellizzeri, Esposito, Morici, Oreglia, Casella, Mauro, Vassilev, Galie, Santulli, Pizzi, Barbato, Calabrò and Marfella. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Cesaro, Arturo
Gragnano, Felice
Paolisso, Pasquale
Bergamaschi, Luca
Gallinoro, Emanuele
Sardu, Celestino
Mileva, Niya
Foà, Alberto
Armillotta, Matteo
Sansonetti, Angelo
Amicone, Sara
Impellizzeri, Andrea
Esposito, Giuseppe
Morici, Nuccia
Oreglia, Jacopo Andrea
Casella, Gianni
Mauro, Ciro
Vassilev, Dobrin
Galie, Nazzareno
Santulli, Gaetano
Pizzi, Carmine
Barbato, Emanuele
Calabrò, Paolo
Marfella, Raffaele
In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title_full In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title_fullStr In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title_full_unstemmed In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title_short In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study
title_sort in-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with sglt2-inhibitors: insights from the sglt2-i ami protect study
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551177/
https://www.ncbi.nlm.nih.gov/pubmed/36237914
http://dx.doi.org/10.3389/fcvm.2022.1012220
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