| Literature DB >> 30843294 |
Rosalie A Scholtes1, Michaël J B van Baar1, Yuliya Lytvyn2, Petter Bjornstad3,4, Max Nieuwdorp1,5, David Z I Cherney2, Daniël H van Raalte1,5.
Abstract
Sodium glucose cotransporter (SGLT)-2 inhibitors are the newest addition to our treatment armamentarium for the management of hyperglycemia in type 2 diabetes. Glucose-lowering per se reduces the risk of microvascular complications, but not the risk of cardiovascular disease, including heart failure and cardiovascular mortality. Also, even when embedded in optimal cardiovascular prevention, a large residual risk remains with respect to progression of diabetic kidney disease. SGLT-2 inhibitors lower blood glucose levels by inducing glucosuria. Through various proposed mechanisms, among which diuretic and natriuretic effects, SGLT-2 inhibitors decrease heart failure hospitalization, reduce cardiovascular mortality, and mitigate progression of diabetic kidney disease. In this perspective, we will discuss the glucose-lowering and other protective effects of SGLT-2 inhibitors on the cardiorenal axis, both in primary and secondary prevention. By comparing the glycemic and pleiotropic effects of these agents to other glucose-lowering drugs, we will address questions around whether SGLT-2 inhibitors should be considered primarily as glucose-lowering agents, cardiorenal drugs or both.Entities:
Keywords: SGLT-2 inhibition; diabetic kidney disease; glycemic control; heart failure; number-needed-to-treat; primary prevention; secondary prevention
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Year: 2019 PMID: 30843294 PMCID: PMC7045873 DOI: 10.1111/dom.13692
Source DB: PubMed Journal: Diabetes Obes Metab ISSN: 1462-8902 Impact factor: 6.577