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Serum Irisin Predicts Mortality Risk in Acute Heart Failure Patients

Authors :
Shutong Shen
Rongrong Gao
Yihua Bei
Jin Li
Haifeng Zhang
Yanli Zhou
Wenming Yao
Dongjie Xu
Fang Zhou
Mengchao Jin
Siqi Wei
Kai Wang
Xuejuan Xu
Yongqin Li
Junjie Xiao
Xinli Li
Source :
Cellular Physiology and Biochemistry, Vol 42, Iss 2, Pp 615-622 (2017)
Publication Year :
2017
Publisher :
Cell Physiol Biochem Press GmbH & Co KG, 2017.

Abstract

Background/Aims: Irisin is a peptide hormone cleaved from a plasma membrane protein fibronectin type III domain containing protein 5 (FNDC5). Emerging studies have indicated association between serum irisin and many major chronic diseases including cardiovascular diseases. However, the role of serum irisin as a predictor for mortality risk in acute heart failure (AHF) patients is not clear. Methods: AHF patients were enrolled and serum was collected at the admission and all patients were followed up for 1 year. Enzyme-linked immunosorbent assay was used to measure serum irisin levels. To explore predictors for AHF mortality, the univariate and multivariate logistic regression analysis, and receiver-operator characteristic (ROC) curve analysis were used. To determine the role of serum irisin levels in predicting survival, Kaplan-Meier survival analysis was used. Results: In this study, 161 AHF patients were enrolled and serum irisin level was found to be significantly higher in patients deceased in 1-year follow-up. The univariate logistic regression analysis identified 18 variables associated with all-cause mortality in AHF patients, while the multivariate logistic regression analysis identified 2 variables namely blood urea nitrogen and serum irisin. ROC curve analysis indicated that blood urea nitrogen and the most commonly used biomarker, NT-pro-BNP, displayed poor prognostic value for AHF (AUCs ≤ 0.700) compared to serum irisin (AUC = 0.753). Kaplan-Meier survival analysis demonstrated that AHF patients with higher serum irisin had significantly higher mortality (P

Details

Language :
English
ISSN :
10158987 and 14219778
Volume :
42
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Cellular Physiology and Biochemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.4366de4bcaf641bf9fd860d6e5488e3b
Document Type :
article
Full Text :
https://doi.org/10.1159/000477867