Growth differentiation factor-15 is not modified by sacubitril/valsartan and is an independent marker of risk in patients with heart failure and reduced ejection fraction: the PARADIGM-HF trial

被引:74
作者
Bouabdallaoui, Nadia [1 ,2 ]
Claggett, Brian [3 ]
Zile, Michael R. [4 ,5 ]
McMurray, John J. V. [6 ]
O'Meara, Eileen [1 ,2 ]
Packer, Milton [7 ]
Prescott, Margarett F. [8 ]
Swedberg, Karl [9 ]
Solomon, Scott D. [3 ]
Rouleau, Jean L. [1 ,2 ]
机构
[1] Montreal Heart Inst, 5000 Belanger St, Montreal, PQ H1T 1C8, Canada
[2] Univ Montreal, Montreal, PQ, Canada
[3] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[4] Med Univ South Carolina, Charleston, SC USA
[5] Ralph H Johnson Vet Adm Med Ctr, Charleston, SC USA
[6] Univ Glasgow, BHF Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
[7] Baylor Univ, Med Ctr, Dallas, TX USA
[8] Novartis Pharmaceut, E Hanover, NJ USA
[9] Univ Gothenburg, Gothenburg, Sweden
关键词
Heart failure with reduced ejection fraction; GDF-15; Biomarkers; Sacubitril/valsartan; Global risk assessment; Cardiovascular mortality; NEPRILYSIN INHIBITION; CARDIOVASCULAR EVENTS; PREDICTS MORTALITY; BIOMARKERS; INFLAMMATION; ENALAPRIL; FIBROSIS; RECEPTOR; UTILITY; STRESS;
D O I
10.1002/ejhf.1301
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Growth differentiation factor-15 (GDF-15) is associated with adverse prognosis in cardiovascular (CV) and non-CV diseases. We evaluated the association of GDF-15 with CV and non-CV outcomes in the PARADIGM-HF trial. Methods and results In 1935 patients with heart failure and reduced ejection fraction (HFrEF) in PARADIGM-HF, median GDF-15 values were elevated and similar in sacubitril/valsartan and enalapril patients (1626 ng/L and 1690 ng/L, respectively). Diabetes, age, creatinine, high-sensitive troponin T, N-terminal pro-B-type natriuretic peptide, and New York Heart Association class III/IV were most strongly associated with elevated GDF-15 values (all P < 0.001) (adjusted R-2 = 0.3857). Baseline GDF-15 and changes in GDF-15 at both 1 month and 8months (log-transformed) were associated with subsequent mortality and CV events. Each 20% increment in baseline GDF-15 value was associated with a higher risk of mortality [adjusted hazard ratio (HR) 1.13, 95% confidence interval (CI) 1.08-1.18, P < 0.001], the combined endpoint of CV death or hospitalization for heart failure (adjusted HR 1.09, 95% CI 1.05-1.14, P < 0.001) and heart failure death (adjusted HR 1.16, 95% CI 1.05-1.28, P < 0.001). Changes in GDF-15 were not influenced by assigned therapy (all P-values >= 0.1). Conclusion In patients with ambulatory HFrEF, GDF-15 is not modified by sacubitril/valsartan and is strongly associated with mortality and CV outcomes, suggesting that GDF-15 is a marker of poor outcomes in these patients.
引用
收藏
页码:1701 / 1709
页数:9
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