Effect of Dapagliflozin on Heart Failure and Mortality in Type 2 Diabetes Mellitus

被引:467
|
作者
Kato, Eri T. [2 ]
Silverman, Michael G. [3 ]
Mosenzon, Ofri [4 ]
Zelniker, Thomas A. [1 ]
Cahn, Avivit [4 ]
Furtado, Remo H. M. [1 ]
Kuder, Julia [1 ]
Murphy, Sabina A. [1 ]
Bhatt, Deepak L. [1 ]
Leiter, Lawrence A. [5 ]
McGuire, Darren K. [6 ]
Wilding, John P. H. [7 ]
Bonaca, Marc P. [8 ]
Ruff, Christian T. [1 ]
Desai, Akshay S. [9 ]
Goto, Shinya [10 ]
Johansson, Peter A. [11 ]
Gause-Nilsson, Ingrid [11 ]
Johanson, Per [11 ]
Langkilde, Anna Maria [11 ]
Raz, Itamar [4 ]
Sabatine, Marc S. [1 ]
Wiviott, Stephen D. [1 ]
机构
[1] Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 60 Fenwood Rd,Ste 7022, Boston, MA 02115 USA
[2] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Kyoto, Japan
[3] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[4] Hebrew Univ Jerusalem, Fac Med, Hadassah Med Ctr, Diabet Unit,Dept Endocrinol & Metab, Jerusalem, Israel
[5] Univ Toronto, St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[6] Univ Texas Southwestern Med Ctr Dallas, Div Cardiol, Dallas, TX 75390 USA
[7] Univ Liverpool, Inst Ageing & Chron Dis, Liverpool, Merseyside, England
[8] Univ Colorado, CPC Clin Res, Denver, CO 80202 USA
[9] Brigham & Womens Hosp, Div Cardiovasc, 75 Francis St, Boston, MA 02115 USA
[10] Tokai Univ, Dept Med Cardiol, Isehara, Kanagawa, Japan
[11] AstraZeneca, Gothenburg, Sweden
关键词
diabetes mellitus; sodium-glucose transporter 2 inhibitors; heart failure; mortality; CARDIOVASCULAR EVENTS; OUTCOMES; EMPAGLIFLOZIN; ASSOCIATION; DIAGNOSIS; IMPACT;
D O I
10.1161/CIRCULATIONAHA.119.040130
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In DECLARE-TIMI 58 (Dapagliflozin Effect on Cardiovascular Events-Thrombolysis in Myocardial Infarction 58), the sodium-glucose cotransporter 2 inhibitor dapagliflozin reduced the composite end point of cardiovascular death/hospitalization for heart failure (HHF) in a broad population of patients with type 2 diabetes mellitus. However, the impact of baseline left ventricular ejection fraction (EF) on the clinical benefit of sodium-glucose cotransporter 2 inhibition is unknown. Methods: In the DECLARE-TIMI 58 trial, baseline heart failure (HF) status was collected from all patients, and EF was collected when available. HF with reduced EF (HFrEF) was defined as EF <45%. Outcomes of interest were the composite of cardiovascular death/HHF, its components, and all-cause mortality. Results: Of 17 160 patients, 671 (3.9%) had HFrEF, 1316 (7.7%) had HF without known reduced EF, and 15 173 (88.4%) had no history of HF at baseline. Dapagliflozin reduced cardiovascular death/HHF more in patients with HFrEF (hazard ratio [HR], 0.62 [95% CI, 0.45-0.86]) than in those without HFrEF (HR, 0.88 [95% CI, 0.76-1.02]; P for interaction=0.046), in whom the treatment effect of dapagliflozin was similar in those with HF without known reduced EF (HR, 0.88 [95% CI, 0.66-1.17]) and those without HF (HR, 0.88 [95% CI, 0.74-1.03]). Whereas dapagliflozin reduced HHF both in those with (HR, 0.64 [95% CI, 0.43-0.95]) and in those without HFrEF (HR, 0.76 [95% CI, 0.62-0.92]), it reduced cardiovascular death only in patients with HFrEF (HR, 0.55 [95% CI, 0.34-0.90]) but not in those without HFrEF (HR, 1.08 [95% CI, 0.89-1.31]; P for interaction=0.012). Likewise, dapagliflozin reduced all-cause mortality in patients with HFrEF (HR, 0.59 [95% CI, 0.40-0.88;) but not in those without HFrEF (HR, 0.97 [95% CI, 0.86-1.10]; P for interaction=0.016). Conclusions: In the first sodium-glucose cotransporter 2 inhibitor cardiovascular outcome trial to evaluate patients with type 2 diabetes mellitus stratified by EF, we found that dapagliflozin reduced HHF in patients with and without HFrEF and reduced cardiovascular death and all-cause mortality in patients with HFrEF.
引用
收藏
页码:2528 / 2536
页数:9
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