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Therapeutic Advances in Diabetic Kidney Disease
Although sodium glucose co-transporter type 2 (SGLT-2) inhibitors were initially introduced as glucose-lowering medications, it was later discovered that cardiorenal protection is the most important treatment effect of these agents. A triad of landmark trials consistently showed the benefits of SGLT...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917247/ https://www.ncbi.nlm.nih.gov/pubmed/36769113 http://dx.doi.org/10.3390/ijms24032803 |
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author | Georgianos, Panagiotis I. Vaios, Vasilios Eleftheriadis, Theodoros Papachristou, Evangelos Liakopoulos, Vassilios |
author_facet | Georgianos, Panagiotis I. Vaios, Vasilios Eleftheriadis, Theodoros Papachristou, Evangelos Liakopoulos, Vassilios |
author_sort | Georgianos, Panagiotis I. |
collection | PubMed |
description | Although sodium glucose co-transporter type 2 (SGLT-2) inhibitors were initially introduced as glucose-lowering medications, it was later discovered that cardiorenal protection is the most important treatment effect of these agents. A triad of landmark trials consistently showed the benefits of SGLT-2 inhibitors on kidney and cardiovascular outcomes in patients with chronic kidney disease (CKD), irrespective of the presence or absence of Type 2 diabetes (T2D). Furthermore, finerenone is a novel, selective, nonsteroidal mineralocorticoid receptor antagonist (MRA) that safely and effectively improved cardiorenal outcomes in a large Phase 3 clinical trial program that included >13,000 patients with T2D and a wide spectrum of CKD. These two drug categories have shared and distinct mechanisms of action, generating the hypothesis that an overadditive cardiorenal benefit with their combined use may be biologically plausible. In this article, we describe the mechanism of action, and we provide an overview of the evidence for cardiorenal protection with SGLT-2 inhibitors and the nonsteroidal MRA finerenone in patients with CKD associated with T2D. |
format | Online Article Text |
id | pubmed-9917247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99172472023-02-11 Therapeutic Advances in Diabetic Kidney Disease Georgianos, Panagiotis I. Vaios, Vasilios Eleftheriadis, Theodoros Papachristou, Evangelos Liakopoulos, Vassilios Int J Mol Sci Review Although sodium glucose co-transporter type 2 (SGLT-2) inhibitors were initially introduced as glucose-lowering medications, it was later discovered that cardiorenal protection is the most important treatment effect of these agents. A triad of landmark trials consistently showed the benefits of SGLT-2 inhibitors on kidney and cardiovascular outcomes in patients with chronic kidney disease (CKD), irrespective of the presence or absence of Type 2 diabetes (T2D). Furthermore, finerenone is a novel, selective, nonsteroidal mineralocorticoid receptor antagonist (MRA) that safely and effectively improved cardiorenal outcomes in a large Phase 3 clinical trial program that included >13,000 patients with T2D and a wide spectrum of CKD. These two drug categories have shared and distinct mechanisms of action, generating the hypothesis that an overadditive cardiorenal benefit with their combined use may be biologically plausible. In this article, we describe the mechanism of action, and we provide an overview of the evidence for cardiorenal protection with SGLT-2 inhibitors and the nonsteroidal MRA finerenone in patients with CKD associated with T2D. MDPI 2023-02-01 /pmc/articles/PMC9917247/ /pubmed/36769113 http://dx.doi.org/10.3390/ijms24032803 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Georgianos, Panagiotis I. Vaios, Vasilios Eleftheriadis, Theodoros Papachristou, Evangelos Liakopoulos, Vassilios Therapeutic Advances in Diabetic Kidney Disease |
title | Therapeutic Advances in Diabetic Kidney Disease |
title_full | Therapeutic Advances in Diabetic Kidney Disease |
title_fullStr | Therapeutic Advances in Diabetic Kidney Disease |
title_full_unstemmed | Therapeutic Advances in Diabetic Kidney Disease |
title_short | Therapeutic Advances in Diabetic Kidney Disease |
title_sort | therapeutic advances in diabetic kidney disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917247/ https://www.ncbi.nlm.nih.gov/pubmed/36769113 http://dx.doi.org/10.3390/ijms24032803 |
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