Effect of sacubitril/valsartan versus enalapril on glycaemic control in patients with heart failure and diabetes: a post-hoc analysis from the PARADIGM-HF trial

被引:366
作者
Seferovic, Jelena P. [1 ]
Claggett, Brian [1 ]
Seidelmann, Sara B. [1 ]
Seely, Ellen W. [2 ]
Packer, Milton [3 ]
Zile, Michael R. [4 ,5 ]
Rouleau, Jean L. [6 ]
Swedberg, Karl [7 ]
Lefkowitz, Martin [8 ]
Shi, Victor C. [8 ]
Desai, Akshay S. [1 ]
McMurray, John J. V. [9 ]
Solomon, Scott D. [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Endocrinol Diabet & Hypertens Div, Boston, MA USA
[3] Baylor Univ, Med Ctr, Dallas, TX USA
[4] Med Univ South Carolina, Charleston, SC USA
[5] RHJ Dept Vet Adm Med Ctr, Charleston, SC USA
[6] Univ Montreal, Inst Cardiol, Montreal, PQ, Canada
[7] Sahlgrens Univ Hosp, Dept Mol & Clin Med, Gothenburg, Sweden
[8] Novartis Pharmaceut, E Hanover, NJ USA
[9] Univ Glasgow, BHF Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
关键词
ANGIOTENSIN-CONVERTING ENZYME; BASE-LINE CHARACTERISTICS; NATRIURETIC-PEPTIDE; CARDIOVASCULAR OUTCOMES; NEPRILYSIN INHIBITION; INSULIN SENSITIVITY; MORTALITY; MORBIDITY; RISK; CANDESARTAN;
D O I
10.1016/S2213-8587(17)30087-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Diabetes is an independent risk factor for heart failure progression. Sacubitril/valsartan, a combination angiotensin receptor-neprilysin inhibitor, improves morbidity and mortality in patients with heart failure with reduced ejection fraction (HFrEF), compared with the angiotensin-converting enzyme inhibitor enalapril, and improves peripheral insulin sensitivity in obese hypertensive patients. We aimed to investigate the effect of sacubitril/valsartan versus enalapril on HbA(1c) and time to first-time initiation of insulin or oral antihyperglycaemic drugs in patients with diabetes and HFrEF. Methods In a post-hoc analysis of the PARADIGM-HF trial, we included 3778 patients with known diabetes or an HbA(1c) >= 6.5% at screening out of 8399 patients with HFrEF who were randomly assigned to treatment with sacubitril/valsartan or enalapril. Of these patients, most (98%) had type 2 diabetes. We assessed changes in HbA(1c), triglycerides, HDL cholesterol and BMI in a mixed effects longitudinal analysis model. Time to initiation of oral antihyperglycaemic drugs or insulin in subjects previously not treated with these agents were compared between treatment groups. Findings There were no significant differences in HbA(1c) concentrations between randomised groups at screening. During the first year of follow-up, HbA(1c) concentrations decreased by 0.16% (SD 1.40) in the enalapril group and 0.26% (SD 1.25) in the sacubitril/valsartan group (between-group reduction 0.13%, 95% CI 0.05-0.22, p=0.0023). HbA(1c) concentrations were persistently lower in the sacubitril/valsartan group than in the enalapril group over the 3-year follow-up (between-group reduction 0.14%, 95% CI 0.06-0.23, p=0.0055). New use of insulin was 29% lower in patients receiving sacubitril/valsartan (114 [7%] patients) compared with patients receiving enalapril (153 [10%]; hazard ratio 0.71, 95% CI 0.56-0.90, p=0.0052). Similarly, fewer patients were started on oral antihyperglycaemic therapy (0.77, 0.58-1.02, p=0.073) in the sacubitril/valsartan group. Interpretation Patients with diabetes and HFrEF enrolled in PARADIGM-HF who received sacubitril/valsartan had a greater long-term reduction in HbA(1c) than those receiving enalapril. These data suggest that sacubitril/valsartan might enhance glycaemic control in patients with diabetes and HFrEF.
引用
收藏
页码:333 / 340
页数:8
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