| Literature DB >> 31707795 |
Christopher P Cannon1, Vlado Perkovic2, Rajiv Agarwal3, James Baldassarre4, George Bakris5, David M Charytan6, Dick de Zeeuw7, Robert Edwards4, Tom Greene8, Hiddo J L Heerspink9, Meg J Jardine10, Adeera Levin11, Jing-Wei Li12, Bruce Neal13, Carol Pollock14, David C Wheeler15, Hong Zhang16, Bernard Zinman17, Kenneth W Mahaffey18.
Abstract
Traditional management of diabetes mellitus has focused on glycemic control, beginning with lifestyle changes, followed by metformin, and then other classes of antiglycemic agents.1 Sodium glucose co-transporter 2 (SGLT2) inhibitors reduce cardiovascular (CV) events, including CV death, myocardial infarction (MI) and heart failure, and slow progression of renal dysfunction, including prevention of end-stage kidney disease (ESKD).2-3 Because initial clinical trials included mostly patients with baseline HbA1c >7%, current guidelines have recommended this class as add-on therapy for patients whose HbA1c is not at goal, typically ≥7%.1 We hypothesized that there would be similar benefits on CV and renal endpoints regardless of baseline HbA1c, including those with HbA1c <7%.Entities:
Year: 2019 PMID: 31707795 DOI: 10.1161/CIRCULATIONAHA.119.044359
Source DB: PubMed Journal: Circulation ISSN: 0009-7322 Impact factor: 29.690