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Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study

AIMS: Sodium‐glucose cotransporter type 2 inhibitors (SGLT‐2i) represent a unique class of anti‐hyperglycaemic agents for type 2 diabetes mellitus that selectively inhibit renal glucose reabsorption, thereby increasing urinary excretion of glucose. Several studies have demonstrated the cardioprotect...

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Autores principales: Correale, Michele, Antohi, Elena‐Laura, Inciardi, Riccardo M., Mazzeo, Pietro, Coiro, Stefano, Ishihara, Shiro, Petroni, Renata, Monitillo, Francesco, Leone, Marta, Triggiani, Marco, Sarwar, Chaudhry M.S., Dungen, Hans‐Dirk, Talha, Khawaja M., Brunetti, Natale D., Butler, Javed, Nodari, Savina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192273/
https://www.ncbi.nlm.nih.gov/pubmed/36924023
http://dx.doi.org/10.1002/ehf2.14331
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author Correale, Michele
Antohi, Elena‐Laura
Inciardi, Riccardo M.
Mazzeo, Pietro
Coiro, Stefano
Ishihara, Shiro
Petroni, Renata
Monitillo, Francesco
Leone, Marta
Triggiani, Marco
Sarwar, Chaudhry M.S.
Dungen, Hans‐Dirk
Talha, Khawaja M.
Brunetti, Natale D.
Butler, Javed
Nodari, Savina
author_facet Correale, Michele
Antohi, Elena‐Laura
Inciardi, Riccardo M.
Mazzeo, Pietro
Coiro, Stefano
Ishihara, Shiro
Petroni, Renata
Monitillo, Francesco
Leone, Marta
Triggiani, Marco
Sarwar, Chaudhry M.S.
Dungen, Hans‐Dirk
Talha, Khawaja M.
Brunetti, Natale D.
Butler, Javed
Nodari, Savina
author_sort Correale, Michele
collection PubMed
description AIMS: Sodium‐glucose cotransporter type 2 inhibitors (SGLT‐2i) represent a unique class of anti‐hyperglycaemic agents for type 2 diabetes mellitus that selectively inhibit renal glucose reabsorption, thereby increasing urinary excretion of glucose. Several studies have demonstrated the cardioprotective effects of SGLT‐2i in patients with heart failure (HF), unrelated to its glucosuric effect. It is unclear whether the benefits of SGLT‐2i therapy also rely on the improvement of left ventricular (LV) and/or right ventricular (RV) function in patients with HF. This study aimed to evaluate the effect of SGLT‐2i on LV and RV function through conventional and advanced echocardiographic parameters with a special focus on RV function in patients with HF. METHODS AND RESULTS: The Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure (BEGIN‐HF) study is an international multicentre, prospective study that will evaluate the effect of SGLT‐2i on echocardiographic parameters of myocardial function in patients with chronic stable HF across the left ventricular ejection fraction (LVEF) spectrum. Patients with New York Heart Association Class II/III symptoms, estimated glomerular filtration rate > 25 mL/min/1.73 m(2), age > 18 years, and those who were not previously treated with SGLT‐2i will be included. All patients will undergo conventional, tissue‐derived imaging (TDI), and strain echocardiography in an ambulatory setting, at time of enrolment and after 6 months of SGLT‐2i therapy. The primary endpoint is the change in LV function as assessed by conventional, TDI, and myocardial deformation speckle tracking parameters. Secondary outcomes include changes in RV and left atrial function as assessed by conventional and deformation speckle tracking echocardiography. Univariate and multivariate analyses will be performed to identify predictors associated with primary and secondary endpoints. CONCLUSIONS: The BEGIN‐HF will determine whether SGLT‐2i therapy improves LV and/or RV function by conventional and advanced echocardiography in patients with HF irrespective of LVEF.
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spelling pubmed-101922732023-05-19 Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study Correale, Michele Antohi, Elena‐Laura Inciardi, Riccardo M. Mazzeo, Pietro Coiro, Stefano Ishihara, Shiro Petroni, Renata Monitillo, Francesco Leone, Marta Triggiani, Marco Sarwar, Chaudhry M.S. Dungen, Hans‐Dirk Talha, Khawaja M. Brunetti, Natale D. Butler, Javed Nodari, Savina ESC Heart Fail Study Designs AIMS: Sodium‐glucose cotransporter type 2 inhibitors (SGLT‐2i) represent a unique class of anti‐hyperglycaemic agents for type 2 diabetes mellitus that selectively inhibit renal glucose reabsorption, thereby increasing urinary excretion of glucose. Several studies have demonstrated the cardioprotective effects of SGLT‐2i in patients with heart failure (HF), unrelated to its glucosuric effect. It is unclear whether the benefits of SGLT‐2i therapy also rely on the improvement of left ventricular (LV) and/or right ventricular (RV) function in patients with HF. This study aimed to evaluate the effect of SGLT‐2i on LV and RV function through conventional and advanced echocardiographic parameters with a special focus on RV function in patients with HF. METHODS AND RESULTS: The Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure (BEGIN‐HF) study is an international multicentre, prospective study that will evaluate the effect of SGLT‐2i on echocardiographic parameters of myocardial function in patients with chronic stable HF across the left ventricular ejection fraction (LVEF) spectrum. Patients with New York Heart Association Class II/III symptoms, estimated glomerular filtration rate > 25 mL/min/1.73 m(2), age > 18 years, and those who were not previously treated with SGLT‐2i will be included. All patients will undergo conventional, tissue‐derived imaging (TDI), and strain echocardiography in an ambulatory setting, at time of enrolment and after 6 months of SGLT‐2i therapy. The primary endpoint is the change in LV function as assessed by conventional, TDI, and myocardial deformation speckle tracking parameters. Secondary outcomes include changes in RV and left atrial function as assessed by conventional and deformation speckle tracking echocardiography. Univariate and multivariate analyses will be performed to identify predictors associated with primary and secondary endpoints. CONCLUSIONS: The BEGIN‐HF will determine whether SGLT‐2i therapy improves LV and/or RV function by conventional and advanced echocardiography in patients with HF irrespective of LVEF. John Wiley and Sons Inc. 2023-03-15 /pmc/articles/PMC10192273/ /pubmed/36924023 http://dx.doi.org/10.1002/ehf2.14331 Text en © 2023 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Study Designs
Correale, Michele
Antohi, Elena‐Laura
Inciardi, Riccardo M.
Mazzeo, Pietro
Coiro, Stefano
Ishihara, Shiro
Petroni, Renata
Monitillo, Francesco
Leone, Marta
Triggiani, Marco
Sarwar, Chaudhry M.S.
Dungen, Hans‐Dirk
Talha, Khawaja M.
Brunetti, Natale D.
Butler, Javed
Nodari, Savina
Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title_full Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title_fullStr Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title_full_unstemmed Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title_short Rationale and design of the Biventricular Evaluation of Gliflozins effects In chroNic Heart Failure: BEGIN‐HF study
title_sort rationale and design of the biventricular evaluation of gliflozins effects in chronic heart failure: begin‐hf study
topic Study Designs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192273/
https://www.ncbi.nlm.nih.gov/pubmed/36924023
http://dx.doi.org/10.1002/ehf2.14331
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