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Evaluating the Effects of Canagliflozin on Cardiovascular and Renal Events in Patients With Type 2 Diabetes Mellitus and Chronic Kidney Disease According to Baseline HbA1c, Including Those With HbA1c <7%
Author(s) -
Christopher P. Can,
Vlado Perkovic,
Rajiv Agarwal,
James Baldassarre,
George L. Bakris,
David M. Charytan,
Dick de Zeeuw,
Robert Edwards,
Tom Greene,
Hiddo J.L. Heerspink,
Meg Jardine,
Adeera Levin,
Jing-Wei Li,
Bruce Neal,
Carol A. Pollock,
David C. Wheeler,
Hong Zhang,
Bernard Zinman,
Kenneth W. Mahaffey
Publication year - 2019
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.119.044359
Subject(s) - medicine , canagliflozin , diabetes mellitus , kidney disease , type 2 diabetes mellitus , gerontology , family medicine , endocrinology
Traditional management of diabetes mellitus has focused on glycemic control, beginning with lifestyle changes, followed by metformin, and then other classes of antiglycemic agents. 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). 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%. We hypothesized that there would be similar benefits on CV and renal endpoints regardless of baseline HbA1c, including those with HbA1c <7%.

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