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Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors
The number of people living with type 2 diabetes (T2D) and its complications worldwide is increasing at an alarming rate. Fortunately, our understanding of the benefits of glucose-lowering agents from the sodium–glucose co-transporter-2 (SGLT2) inhibitor and glucagon-like peptide-1 (GLP-1) receptor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Touch Medical Media
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835817/ https://www.ncbi.nlm.nih.gov/pubmed/36694888 http://dx.doi.org/10.17925/EE.2022.18.2.106 |
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author | Neumiller, Joshua J Lienhard, Fredrick J Alicic, Radica Z Tuttle, Katherine R |
author_facet | Neumiller, Joshua J Lienhard, Fredrick J Alicic, Radica Z Tuttle, Katherine R |
author_sort | Neumiller, Joshua J |
collection | PubMed |
description | The number of people living with type 2 diabetes (T2D) and its complications worldwide is increasing at an alarming rate. Fortunately, our understanding of the benefits of glucose-lowering agents from the sodium–glucose co-transporter-2 (SGLT2) inhibitor and glucagon-like peptide-1 (GLP-1) receptor agonist classes on cardiovascular and kidney outcomes is advancing; this means we now have new options to mitigate the risks of these complications in patients with T2D. The SGLT2 inhibitors have consistently demonstrated benefits on atherosclerotic cardiovascular disease (ASCVD), chronic kidney disease (CKD) and heart failure (HF) events in dedicated outcome trials. Large guidelines groups now recommend SGLT2 inhibitors as a standard of care in patients with T2D and comorbid ASCVD, CKD and/ or HF. Evolving evidence additionally indicates kidney and HF benefits of SGLT2 inhibitors in populations without diabetes. These agents likely provide heart and kidney benefits through multiple mechanisms, as their impact on heart and kidney outcomes cannot be fully explained by their direct metabolic effects. On-going work to elucidate the beneficial mechanisms at play with SGLT2 inhibitors will help further optimize these life-saving therapies in patients with and without T2D. |
format | Online Article Text |
id | pubmed-9835817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Touch Medical Media |
record_format | MEDLINE/PubMed |
spelling | pubmed-98358172023-01-23 Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors Neumiller, Joshua J Lienhard, Fredrick J Alicic, Radica Z Tuttle, Katherine R touchREV Endocrinol Diabetes The number of people living with type 2 diabetes (T2D) and its complications worldwide is increasing at an alarming rate. Fortunately, our understanding of the benefits of glucose-lowering agents from the sodium–glucose co-transporter-2 (SGLT2) inhibitor and glucagon-like peptide-1 (GLP-1) receptor agonist classes on cardiovascular and kidney outcomes is advancing; this means we now have new options to mitigate the risks of these complications in patients with T2D. The SGLT2 inhibitors have consistently demonstrated benefits on atherosclerotic cardiovascular disease (ASCVD), chronic kidney disease (CKD) and heart failure (HF) events in dedicated outcome trials. Large guidelines groups now recommend SGLT2 inhibitors as a standard of care in patients with T2D and comorbid ASCVD, CKD and/ or HF. Evolving evidence additionally indicates kidney and HF benefits of SGLT2 inhibitors in populations without diabetes. These agents likely provide heart and kidney benefits through multiple mechanisms, as their impact on heart and kidney outcomes cannot be fully explained by their direct metabolic effects. On-going work to elucidate the beneficial mechanisms at play with SGLT2 inhibitors will help further optimize these life-saving therapies in patients with and without T2D. Touch Medical Media 2022-11 2022-11-29 /pmc/articles/PMC9835817/ /pubmed/36694888 http://dx.doi.org/10.17925/EE.2022.18.2.106 Text en © Touch Medical Media 2022 ali:free_to_read www.copyright.com (http://www.copyright.com) Review process: Double-blind peer review. Compliance with ethics: This study involves a review of the literature and did not involve any studies with human or animal subjects performed by any of the authors. Data availability: Data sharing is not applicable to this article as no datasets were generated or analysed during the writing of this article. Authorship: The named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship of this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval for the version to be published. https://creativecommons.org/licenses/by/3.0/Access: This article is freely accessible at touchENDOCRINOLOGY.com (http://touchENDOCRINOLOGY.com) . © Touch Medical Media 2022 |
spellingShingle | Diabetes Neumiller, Joshua J Lienhard, Fredrick J Alicic, Radica Z Tuttle, Katherine R Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title | Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title_full | Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title_fullStr | Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title_full_unstemmed | Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title_short | Clinical Evidence and Proposed Mechanisms for Cardiovascular and Kidney Benefits from Sodium–Glucose Co-transporter-2 Inhibitors |
title_sort | clinical evidence and proposed mechanisms for cardiovascular and kidney benefits from sodium–glucose co-transporter-2 inhibitors |
topic | Diabetes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835817/ https://www.ncbi.nlm.nih.gov/pubmed/36694888 http://dx.doi.org/10.17925/EE.2022.18.2.106 |
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