Association of Arginine Vasopressin Levels With Outcomes and the Effect of V2 Blockade in Patients Hospitalized for Heart Failure With Reduced Ejection Fraction Insights From the EVEREST Trial

被引:57
作者
Lanfear, David E. [1 ]
Sabbah, Hani N. [2 ]
Goldsmith, Steven R. [3 ]
Greene, Stephen J. [4 ]
Ambrosy, Andrew P. [5 ]
Fought, Angela J. [6 ]
Kwasny, Mary J. [6 ]
Swedberg, Karl [7 ]
Yancy, Clyde W. [8 ]
Konstam, Marvin A. [9 ]
Maggioni, Aldo P. [10 ]
Zannad, Faiez [11 ,12 ]
Gheorghiade, Mihai [4 ]
机构
[1] Henry Ford Hosp, Inst Heart & Vasc, Detroit, MI 48202 USA
[2] Henry Ford Hosp, Dept Med, Detroit, MI 48202 USA
[3] Univ Minnesota, Hennepin Cty Med Ctr, Minneapolis, MN 55415 USA
[4] Northwestern Univ, Feinberg Sch Med, Ctr Cardiovasc Innovat, Chicago, IL 60611 USA
[5] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Preventat Med, Chicago, IL 60611 USA
[7] Univ Gothenburg, Sahlgrenska Acad, Dept Mol & Clin Med, Gothenburg, Sweden
[8] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Cardiol, Chicago, IL 60611 USA
[9] Tufts Med Ctr, Ctr Cardiovasc, Boston, MA USA
[10] ANMCO Res Ctr, Florence, Italy
[11] Univ Lorraine, CHU Cardiol, INSERM, CIC 9501, Nancy, France
[12] Univ Lorraine, CHU Cardiol, U961, Nancy, France
关键词
drugs; heart failure; hormones; outcomes; LEFT-VENTRICULAR DYSFUNCTION; DOUBLE-BLIND; NEUROHUMORAL ACTIVATION; ORAL TOLVAPTAN; ANTAGONISM; HYPONATREMIA; MULTICENTER;
D O I
10.1161/CIRCHEARTFAILURE.112.970012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Arginine vasopressin (AVP) levels are elevated in proportion to heart failure severity and are associated with higher cardiovascular mortality in ambulatory patients. However, the relationship between baseline and trends in AVP with outcomes in patients hospitalized for worsening heart failure with reduced ejection fraction is unclear. Methods and Results-The Efficacy of Vasopressin Antagonism in Heart Failure Outcome Study with Tolvaptan (EVEREST) trial investigated the effects of tolvaptan in patients with worsening heart failure and ejection fraction <= 40%. The present analysis examined baseline and follow-up AVP levels in 3196 EVEREST patients with valid AVP measurements. Coprimary end points included all-cause mortality, and the composite of cardiovascular mortality or heart failure hospitalization. Median follow-up was 9.9 months. Times to events were compared with univariate log-rank tests and multivariable Cox regression models, adjusted for baseline risk factors. After adjusting for baseline covariates, elevated AVP levels were associated with increased all-cause mortality (hazard ratio, 1.33; 95% confidence interval, 1.13-1.55) and cardiovascular mortality or heart failure hospitalization (hazard ratio, 1.23; 95% confidence interval, 1.08-1.39). There was no interaction of baseline AVP with treatment assignment in terms of survival (P=0.515). Tolvaptan therapy increased the proportion of patients with elevated AVP (P<0.001), but this had no effect on mortality (hazard ratio, 0.95; 95% confidence interval, 0.72-1.24). Conclusions-Elevated baseline AVP level was independently predictive of mortality, but did not identify a group of patients who had improved outcomes with tolvaptan treatment. Tolvaptan treatment increased AVP levels during follow-up, but this incremental increase was not associated with worsened outcomes.
引用
收藏
页码:47 / 52
页数:6
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