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The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction
Sodium-glucose cotransporter type 2 (SGLT2) inhibitors are a relatively new class of antihyperglycemic drug with salutary effects on glucose control, body weight, and blood pressure. Emerging evidence now indicates that these drugs may have a beneficial effect on outcomes in heart failure with reduc...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010852/ https://www.ncbi.nlm.nih.gov/pubmed/33779401 http://dx.doi.org/10.1177/17539447211002678 |
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author | Genuardi, Michael V. Mather, Paul J. |
author_facet | Genuardi, Michael V. Mather, Paul J. |
author_sort | Genuardi, Michael V. |
collection | PubMed |
description | Sodium-glucose cotransporter type 2 (SGLT2) inhibitors are a relatively new class of antihyperglycemic drug with salutary effects on glucose control, body weight, and blood pressure. Emerging evidence now indicates that these drugs may have a beneficial effect on outcomes in heart failure with reduced ejection fraction (HFrEF). Post-approval cardiovascular outcomes data for three of these agents (canagliflozin, empagliflozin, and dapagliflozin) showed an unexpected improvement in cardiovascular endpoints, including heart failure hospitalization and mortality, among patients with type 2 diabetes mellitus (T2DM) and established cardiovascular disease or risk factors. These studies were followed by a placebo controlled trial of dapagliflozin in patients with HFrEF both with and without T2DM, showing a reduction in all-cause mortality comparable to current guideline-directed HFrEF medical therapies such as angiotensin-converting enzyme inhibitors and beta-blockers. In this review, we discuss the current landscape of evidence, safety and adverse effects, and proposed mechanisms of action for use of these agents for patients with HFrEF. The United States (US) and European guidelines are reviewed, as are the current US federally approved indications for each SGLT2 inhibitor. Use of these agents in clinical practice may be limited by an uncertain insurance environment, especially in patients without T2DM. Finally, we discuss practical considerations for the cardiovascular clinician, including within-class differences of the SGLT2 inhibitors currently available on the US market (217/300). |
format | Online Article Text |
id | pubmed-8010852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-80108522021-04-13 The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction Genuardi, Michael V. Mather, Paul J. Ther Adv Cardiovasc Dis Review Sodium-glucose cotransporter type 2 (SGLT2) inhibitors are a relatively new class of antihyperglycemic drug with salutary effects on glucose control, body weight, and blood pressure. Emerging evidence now indicates that these drugs may have a beneficial effect on outcomes in heart failure with reduced ejection fraction (HFrEF). Post-approval cardiovascular outcomes data for three of these agents (canagliflozin, empagliflozin, and dapagliflozin) showed an unexpected improvement in cardiovascular endpoints, including heart failure hospitalization and mortality, among patients with type 2 diabetes mellitus (T2DM) and established cardiovascular disease or risk factors. These studies were followed by a placebo controlled trial of dapagliflozin in patients with HFrEF both with and without T2DM, showing a reduction in all-cause mortality comparable to current guideline-directed HFrEF medical therapies such as angiotensin-converting enzyme inhibitors and beta-blockers. In this review, we discuss the current landscape of evidence, safety and adverse effects, and proposed mechanisms of action for use of these agents for patients with HFrEF. The United States (US) and European guidelines are reviewed, as are the current US federally approved indications for each SGLT2 inhibitor. Use of these agents in clinical practice may be limited by an uncertain insurance environment, especially in patients without T2DM. Finally, we discuss practical considerations for the cardiovascular clinician, including within-class differences of the SGLT2 inhibitors currently available on the US market (217/300). SAGE Publications 2021-03-29 /pmc/articles/PMC8010852/ /pubmed/33779401 http://dx.doi.org/10.1177/17539447211002678 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Genuardi, Michael V. Mather, Paul J. The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title | The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title_full | The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title_fullStr | The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title_full_unstemmed | The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title_short | The dawn of the four-drug era? SGLT2 inhibition in heart failure with reduced ejection fraction |
title_sort | dawn of the four-drug era? sglt2 inhibition in heart failure with reduced ejection fraction |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010852/ https://www.ncbi.nlm.nih.gov/pubmed/33779401 http://dx.doi.org/10.1177/17539447211002678 |
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