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Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach

Introduction: Sodium-glucose cotransporter type 2 inhibitors (SGLT2i), gliflozins, play an emerging role for the treatment of heart failure with reduced left ventricular ejection fraction (HFrEF). Nevertheless, the effects of SGLT2i on ventricular remodeling and function have not been completely und...

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Autores principales: Mele, Marco, Imbrici, Paola, Mele, Antonietta, Togo, Maria Vittoria, Dinoi, Giorgia, Correale, Michele, Brunetti, Natale Daniele, Nicolotti, Orazio, De Luca, Annamaria, Altomare, Cosimo Damiano, Liantonio, Antonella, Amoroso, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289166/
https://www.ncbi.nlm.nih.gov/pubmed/37361206
http://dx.doi.org/10.3389/fphar.2023.1175606
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author Mele, Marco
Imbrici, Paola
Mele, Antonietta
Togo, Maria Vittoria
Dinoi, Giorgia
Correale, Michele
Brunetti, Natale Daniele
Nicolotti, Orazio
De Luca, Annamaria
Altomare, Cosimo Damiano
Liantonio, Antonella
Amoroso, Nicola
author_facet Mele, Marco
Imbrici, Paola
Mele, Antonietta
Togo, Maria Vittoria
Dinoi, Giorgia
Correale, Michele
Brunetti, Natale Daniele
Nicolotti, Orazio
De Luca, Annamaria
Altomare, Cosimo Damiano
Liantonio, Antonella
Amoroso, Nicola
author_sort Mele, Marco
collection PubMed
description Introduction: Sodium-glucose cotransporter type 2 inhibitors (SGLT2i), gliflozins, play an emerging role for the treatment of heart failure with reduced left ventricular ejection fraction (HFrEF). Nevertheless, the effects of SGLT2i on ventricular remodeling and function have not been completely understood yet. Explainable artificial intelligence represents an unprecedented explorative option to clinical research in this field. Based on echocardiographic evaluations, we identified some key clinical responses to gliflozins by employing a machine learning approach. Methods: Seventy-eight consecutive diabetic outpatients followed for HFrEF were enrolled in the study. Using a random forests classification, a single subject analysis was performed to define the profile of patients treated with gliflozins. An explainability analysis using Shapley values was used to outline clinical parameters that mostly improved after gliflozin therapy and machine learning runs highlighted specific variables predictive of gliflozin response. Results: The five-fold cross-validation analyses showed that gliflozins patients can be identified with a 0.70 ± 0.03% accuracy. The most relevant parameters distinguishing gliflozins patients were Right Ventricular S'-Velocity, Left Ventricular End Systolic Diameter and E/e' ratio. In addition, low Tricuspid Annular Plane Systolic Excursion values along with high Left Ventricular End Systolic Diameter and End Diastolic Volume values were associated to lower gliflozin efficacy in terms of anti-remodeling effects. Discussion: In conclusion, a machine learning analysis on a population of diabetic patients with HFrEF showed that SGLT2i treatment improved left ventricular remodeling, left ventricular diastolic and biventricular systolic function. This cardiovascular response may be predicted by routine echocardiographic parameters, with an explainable artificial intelligence approach, suggesting a lower efficacy in case of advanced stages of cardiac remodeling.
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spelling pubmed-102891662023-06-24 Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach Mele, Marco Imbrici, Paola Mele, Antonietta Togo, Maria Vittoria Dinoi, Giorgia Correale, Michele Brunetti, Natale Daniele Nicolotti, Orazio De Luca, Annamaria Altomare, Cosimo Damiano Liantonio, Antonella Amoroso, Nicola Front Pharmacol Pharmacology Introduction: Sodium-glucose cotransporter type 2 inhibitors (SGLT2i), gliflozins, play an emerging role for the treatment of heart failure with reduced left ventricular ejection fraction (HFrEF). Nevertheless, the effects of SGLT2i on ventricular remodeling and function have not been completely understood yet. Explainable artificial intelligence represents an unprecedented explorative option to clinical research in this field. Based on echocardiographic evaluations, we identified some key clinical responses to gliflozins by employing a machine learning approach. Methods: Seventy-eight consecutive diabetic outpatients followed for HFrEF were enrolled in the study. Using a random forests classification, a single subject analysis was performed to define the profile of patients treated with gliflozins. An explainability analysis using Shapley values was used to outline clinical parameters that mostly improved after gliflozin therapy and machine learning runs highlighted specific variables predictive of gliflozin response. Results: The five-fold cross-validation analyses showed that gliflozins patients can be identified with a 0.70 ± 0.03% accuracy. The most relevant parameters distinguishing gliflozins patients were Right Ventricular S'-Velocity, Left Ventricular End Systolic Diameter and E/e' ratio. In addition, low Tricuspid Annular Plane Systolic Excursion values along with high Left Ventricular End Systolic Diameter and End Diastolic Volume values were associated to lower gliflozin efficacy in terms of anti-remodeling effects. Discussion: In conclusion, a machine learning analysis on a population of diabetic patients with HFrEF showed that SGLT2i treatment improved left ventricular remodeling, left ventricular diastolic and biventricular systolic function. This cardiovascular response may be predicted by routine echocardiographic parameters, with an explainable artificial intelligence approach, suggesting a lower efficacy in case of advanced stages of cardiac remodeling. Frontiers Media S.A. 2023-06-09 /pmc/articles/PMC10289166/ /pubmed/37361206 http://dx.doi.org/10.3389/fphar.2023.1175606 Text en Copyright © 2023 Mele, Imbrici, Mele, Togo, Dinoi, Correale, Brunetti, Nicolotti, De Luca, Altomare, Liantonio and Amoroso. 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 Pharmacology
Mele, Marco
Imbrici, Paola
Mele, Antonietta
Togo, Maria Vittoria
Dinoi, Giorgia
Correale, Michele
Brunetti, Natale Daniele
Nicolotti, Orazio
De Luca, Annamaria
Altomare, Cosimo Damiano
Liantonio, Antonella
Amoroso, Nicola
Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title_full Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title_fullStr Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title_full_unstemmed Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title_short Short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
title_sort short-term anti-remodeling effects of gliflozins in diabetic patients with heart failure and reduced ejection fraction: an explainable artificial intelligence approach
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289166/
https://www.ncbi.nlm.nih.gov/pubmed/37361206
http://dx.doi.org/10.3389/fphar.2023.1175606
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