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New hypoglycemic agents and the kidney: what do the major trials tell us?
As the burden of diabetic kidney disease continues to expand, new therapies to preserve renal function or prevent diabetic nephropathy are urgently needed. In the past decade, a number of new hypoglycemic classes have emerged, each with a unique profile of action and benefits. Here we review the imp...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259591/ https://www.ncbi.nlm.nih.gov/pubmed/30542615 http://dx.doi.org/10.12688/f1000research.16135.1 |
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author | Smyth, Brendan Perkovic, Vlado |
author_facet | Smyth, Brendan Perkovic, Vlado |
author_sort | Smyth, Brendan |
collection | PubMed |
description | As the burden of diabetic kidney disease continues to expand, new therapies to preserve renal function or prevent diabetic nephropathy are urgently needed. In the past decade, a number of new hypoglycemic classes have emerged, each with a unique profile of action and benefits. Here we review the impact of glycemic control on renal outcomes and the results of the major clinical trials of glucagon-like peptide 1 (GLP-1) agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors, and sodium–glucose co-transporter 2 (SGLT2) inhibitors. Both GLP-1 agonists and SGLT2 inhibitors consistently demonstrate renal benefits. Further studies of these new agents in different patient groups and in comparison to (or in combination with) other treatments are required to better define their role in combating the burden of diabetic kidney disease. |
format | Online Article Text |
id | pubmed-6259591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-62595912018-12-11 New hypoglycemic agents and the kidney: what do the major trials tell us? Smyth, Brendan Perkovic, Vlado F1000Res Review As the burden of diabetic kidney disease continues to expand, new therapies to preserve renal function or prevent diabetic nephropathy are urgently needed. In the past decade, a number of new hypoglycemic classes have emerged, each with a unique profile of action and benefits. Here we review the impact of glycemic control on renal outcomes and the results of the major clinical trials of glucagon-like peptide 1 (GLP-1) agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors, and sodium–glucose co-transporter 2 (SGLT2) inhibitors. Both GLP-1 agonists and SGLT2 inhibitors consistently demonstrate renal benefits. Further studies of these new agents in different patient groups and in comparison to (or in combination with) other treatments are required to better define their role in combating the burden of diabetic kidney disease. F1000 Research Limited 2018-11-23 /pmc/articles/PMC6259591/ /pubmed/30542615 http://dx.doi.org/10.12688/f1000research.16135.1 Text en Copyright: © 2018 Smyth B and Perkovic V http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Smyth, Brendan Perkovic, Vlado New hypoglycemic agents and the kidney: what do the major trials tell us? |
title | New hypoglycemic agents and the kidney: what do the major trials tell us? |
title_full | New hypoglycemic agents and the kidney: what do the major trials tell us? |
title_fullStr | New hypoglycemic agents and the kidney: what do the major trials tell us? |
title_full_unstemmed | New hypoglycemic agents and the kidney: what do the major trials tell us? |
title_short | New hypoglycemic agents and the kidney: what do the major trials tell us? |
title_sort | new hypoglycemic agents and the kidney: what do the major trials tell us? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259591/ https://www.ncbi.nlm.nih.gov/pubmed/30542615 http://dx.doi.org/10.12688/f1000research.16135.1 |
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