Baseline and serial measurements of galectin-3 in patients with heart failure: relationship to prognosis and effect of treatment with valsartan in the Val-HeFT

被引:119
作者
Anand, Inder S. [1 ,2 ]
Rector, Thomas S. [1 ,2 ]
Kuskowski, Michael [1 ]
Adourian, Aram [3 ]
Muntendam, Pieter [3 ]
Cohn, Jay N. [2 ]
机构
[1] VA Med Ctr, Minneapolis, MN 55417 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] BG Med, Waltham, MA USA
关键词
Heart failure; Biomarkers; Prognosis; Natriuretic peptides; Fibrosis; Pathophysiology; BRAIN NATRIURETIC PEPTIDE; FIBROSIS; TRIAL; MACROPHAGES; PROGRESSION; MORTALITY; THERAPY; MARKER; HF;
D O I
10.1093/eurjhf/hfs205
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was conducted to determine whether galectin-3, a -galactoside-binding lectin, plays a role in the pathogenesis of heart failure (HF). Galectin-3 was measured at baseline (n 1650), after 4 months (n 1346), and after 12 months (n 1097) in the Valsartan Heart Failure Trial (Val-HeFT). Galectin-3 levels at baseline ranged from 4.8 to 53 ng/mL. Higher levels were associated with features of worse HF. In a fully adjusted Cox regression model comprising 23 other prognostic variables, baseline galectin-3 was not associated with the risks of all-cause mortality, the composite of the first morbid event, or hospitalization for HF. However, when changes in galectin-3 over time were examined, the increases in galectin-3 between baseline and 4 months were independently and significantly associated with the risks of subsequent all-cause mortality, first morbid event, and hospitalizations for HF, even after adjusting for all baseline and concurrent changes in all variables including estimated glomerular filtration rate (eGFR) and NT-proBNP. The strongest correlate of galectin-3 levels was eGFR, which accounted for 20 of the variability in galectin-3 levels at baseline. There was a significant interaction (P 0.03) between baseline galectin-3 and the effect of valsartan on hospitalizations for HF. Valsartan caused a significant 44 reduction in hospitalizations for HF in patients with galectin-3 levels below the median level of 16.2 ng/mL, but not in patients with levels above the median. Galectin-3 levels are elevated in a substantial proportion of patients with HF, particularly those with more severe HF and renal dysfunction. Galectin-3 increased over time in this cohort, and the increase was independently associated with worse outcomes. Valsartan use was associated with a reduction in hospitalizations for HF in patients with low galectin-3, but not in those with higher levels of galectin-3.
引用
收藏
页码:511 / 518
页数:8
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