| Literature DB >> 30753708 |
Pantelis Sarafidis1, Charles J Ferro2, Enrique Morales3, Alberto Ortiz4, Jolanta Malyszko5, Radovan Hojs6, Khaled Khazim7, Robert Ekart6, Jose Valdivielso8, Denis Fouque9, Gérard M London10, Ziad Massy11, Petro Ruggenenti12, Esteban Porrini13, Andrej Wiecek14, Carmine Zoccali15, Francesca Mallamaci15, Mads Hornum16.
Abstract
Chronic kidney disease (CKD) in patients with diabetes mellitus (DM) is a major problem of public health. Currently, many of these patients experience progression of cardiovascular and renal disease, even when receiving optimal treatment. In previous years, several new drug classes for the treatment of type 2 DM have emerged, including inhibitors of renal sodium-glucose co-transporter-2 (SGLT-2) and glucagon-like peptide-1 (GLP-1) receptor agonists. Apart from reducing glycaemia, these classes were reported to have other beneficial effects for the cardiovascular and renal systems, such as weight loss and blood pressure reduction. Most importantly, in contrast to all previous studies with anti-diabetic agents, a series of recent randomized, placebo-controlled outcome trials showed that SGLT-2 inhibitors and GLP-1 receptor agonists are able to reduce cardiovascular events and all-cause mortality, as well as progression of renal disease, in patients with type 2 DM. This document presents in detail the available evidence on the cardioprotective and nephroprotective effects of SGLT-2 inhibitors and GLP-1 analogues, analyses the potential mechanisms involved in these actions and discusses their place in the treatment of patients with CKD and DM.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30753708 DOI: 10.1093/ndt/gfy407
Source DB: PubMed Journal: Nephrol Dial Transplant ISSN: 0931-0509 Impact factor: 5.992