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Urinary liver‐type fatty acid‐binding protein as a prognostic marker in patients with acute heart failure

Authors :
Tsutomu Sunayama
Shoichiro Yatsu
Yuya Matsue
Taishi Dotare
Daichi Maeda
Sayaki Ishiwata
Yutaka Nakamura
Shoko Suda
Takao Kato
Masaru Hiki
Takatoshi Kasai
Tohru Minamino
Source :
ESC Heart Failure, Vol 9, Iss 1, Pp 442-449 (2022), ESC Heart Failure
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Aims Urinary liver‐type fatty acid‐binding protein (L‐FABP) is expressed in proximal tubular epithelial cells and excreted into the urine during tubular injury. We hypothesized that high urinary L‐FABP is associated with poor prognosis in patients with acute heart failure (AHF). Methods and results We analysed 623 patients (74 ± 13 years old; 60.0% male patients) with AHF. Urinary L‐FABP levels were measured at the time of admission and adjusted for the urinary creatinine concentration. The primary endpoint was all‐cause mortality. The median value and interquartile range of urinary L‐FABP levels were 6.66 and 3.37–21.1 μg/gCr, respectively. Urinary L‐FABP levels were significantly correlated with both beta‐2 microglobulin and cystatin C levels; the correlation with the former was higher than that with the latter. During the follow‐up of 631 (interquartile range: 387–875) days, 142 deaths occurred. A high tertile of urinary L‐FABP level was associated with high mortality; this association was retained after adjusting for other covariates (second tertile hazard ratio 1.40, P = 0.152 vs. first tertile; third tertile hazard ratio 1.94, P = 0.005 vs. first tertile). Conclusions Urinary L‐FABP is more closely associated with tubular dysfunction than with glomerular dysfunction. Tubular dysfunction, which was evaluated based on urinary L‐FABP levels, in patients with AHF is associated with all‐cause mortality and is independent of pre‐existing risk factors. L‐FABP should be considered for use in the prognosis of AHF.

Details

Language :
English
ISSN :
20555822
Volume :
9
Issue :
1
Database :
OpenAIRE
Journal :
ESC Heart Failure
Accession number :
edsair.doi.dedup.....24bfee35d62c1da8f3d855020178507f