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The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis

AIMS: Recent randomised controlled trials (RCTs) have shown a significant prognostic benefit of sodium-glucose cotransporter 2 (SGLT2) inhibitors in the cardiovascular (CV) profile of patients with diabetes. This systematic review and meta-analysis aim to provide a concise evaluation of all the avai...

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Autores principales: Tsampasian, Vasiliki, Baral, Ranu, Chattopadhyay, Rahul, Debski, Maciej, Joshi, Shruti S, Reinhold, Johannes, Dweck, Marc R, Garg, Pankaj, Vassiliou, Vassilios S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397556/
https://www.ncbi.nlm.nih.gov/pubmed/34457360
http://dx.doi.org/10.1155/2021/9927533
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author Tsampasian, Vasiliki
Baral, Ranu
Chattopadhyay, Rahul
Debski, Maciej
Joshi, Shruti S
Reinhold, Johannes
Dweck, Marc R
Garg, Pankaj
Vassiliou, Vassilios S
author_facet Tsampasian, Vasiliki
Baral, Ranu
Chattopadhyay, Rahul
Debski, Maciej
Joshi, Shruti S
Reinhold, Johannes
Dweck, Marc R
Garg, Pankaj
Vassiliou, Vassilios S
author_sort Tsampasian, Vasiliki
collection PubMed
description AIMS: Recent randomised controlled trials (RCTs) have shown a significant prognostic benefit of sodium-glucose cotransporter 2 (SGLT2) inhibitors in the cardiovascular (CV) profile of patients with diabetes. This systematic review and meta-analysis aim to provide a concise evaluation of all the available evidence for the use of these agents in patients with heart failure (HF) regardless of their baseline diabetes status. METHODS AND RESULTS: PubMed, Web of Science, and Cochrane library databases were systematically searched from inception until November 20(th) 2020. Eight studies consisting of 13,275 patients were included in the meta-analysis. For the total population, SGLT2 inhibitors reduced the risk of all-cause mortality (HR: 0.83; 95% CI: 0.75–0.91; I(2) 0%), hospitalisation for HF (HR: 0.68; 95% CI: 0.61–0.75; I(2): 0%), CV death (HR: 0.82; 95% CI: 0.74–0.92; I(2): 0%), and hospitalisation for HF or CV death (HR: 0.72; 95% CI: 0.66–0.78; I(2): 0%). Subgroup analyses of the total population according to the diabetes status showed that SGLT2 inhibitors significantly reduced the risk of hospitalisation for HF (HR: 0.68; 95% CI: 0.61, 0.75; I(2): 0%), as well as the risk of hospitalisation for HF or CV death (HR: 0.72; 95% CI: 0.66, 078; I(2): 0%) and CV death (HR: 0.82; 95% CI: 0.74, 0.91; I(2): 0%). CONCLUSIONS: The results of this meta-analysis confirm the growing evidence in the literature of the favourable profile of SGLT2 inhibitors in cardiovascular outcomes and mortality in patients with heart failure regardless of the baseline diabetes status. This systematic review has been registered with PROSPERO (CRD42021224777).
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spelling pubmed-83975562021-08-28 The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis Tsampasian, Vasiliki Baral, Ranu Chattopadhyay, Rahul Debski, Maciej Joshi, Shruti S Reinhold, Johannes Dweck, Marc R Garg, Pankaj Vassiliou, Vassilios S Cardiol Res Pract Review Article AIMS: Recent randomised controlled trials (RCTs) have shown a significant prognostic benefit of sodium-glucose cotransporter 2 (SGLT2) inhibitors in the cardiovascular (CV) profile of patients with diabetes. This systematic review and meta-analysis aim to provide a concise evaluation of all the available evidence for the use of these agents in patients with heart failure (HF) regardless of their baseline diabetes status. METHODS AND RESULTS: PubMed, Web of Science, and Cochrane library databases were systematically searched from inception until November 20(th) 2020. Eight studies consisting of 13,275 patients were included in the meta-analysis. For the total population, SGLT2 inhibitors reduced the risk of all-cause mortality (HR: 0.83; 95% CI: 0.75–0.91; I(2) 0%), hospitalisation for HF (HR: 0.68; 95% CI: 0.61–0.75; I(2): 0%), CV death (HR: 0.82; 95% CI: 0.74–0.92; I(2): 0%), and hospitalisation for HF or CV death (HR: 0.72; 95% CI: 0.66–0.78; I(2): 0%). Subgroup analyses of the total population according to the diabetes status showed that SGLT2 inhibitors significantly reduced the risk of hospitalisation for HF (HR: 0.68; 95% CI: 0.61, 0.75; I(2): 0%), as well as the risk of hospitalisation for HF or CV death (HR: 0.72; 95% CI: 0.66, 078; I(2): 0%) and CV death (HR: 0.82; 95% CI: 0.74, 0.91; I(2): 0%). CONCLUSIONS: The results of this meta-analysis confirm the growing evidence in the literature of the favourable profile of SGLT2 inhibitors in cardiovascular outcomes and mortality in patients with heart failure regardless of the baseline diabetes status. This systematic review has been registered with PROSPERO (CRD42021224777). Hindawi 2021-08-19 /pmc/articles/PMC8397556/ /pubmed/34457360 http://dx.doi.org/10.1155/2021/9927533 Text en Copyright © 2021 Vasiliki Tsampasian et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tsampasian, Vasiliki
Baral, Ranu
Chattopadhyay, Rahul
Debski, Maciej
Joshi, Shruti S
Reinhold, Johannes
Dweck, Marc R
Garg, Pankaj
Vassiliou, Vassilios S
The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title_full The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title_fullStr The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title_full_unstemmed The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title_short The Role of SGLT2 Inhibitors in Heart Failure: A Systematic Review and Meta-Analysis
title_sort role of sglt2 inhibitors in heart failure: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397556/
https://www.ncbi.nlm.nih.gov/pubmed/34457360
http://dx.doi.org/10.1155/2021/9927533
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