Abstract

Objective The aim of this study was to evaluate the roles of fibroblast growth factor 21 (FGF21) in heart failure patients with reduced ejection fraction and its association with Heart Failure with reduced Ejection Fraction (HFrEF). Methods The level of FGF21 was measured by enzyme-linked immunosorbent assay (ELISA) in 199 subjects enrolled in this study, including 128 subjects with HFrEF and 71 control subjects. The mean follow-up time was 13.36 months. The left ventricular end-diastolic diameter (LVEDD) and left ventricular ejection fraction (LVEF) percentage were evaluated by the 2D echocardiography. Serum brain natriuretic peptide (BNP) was measured in the routine clinical laboratory. Results The serum FGF21 level was evidently higher in patients with HFrEF than in the control group (228.72 ± 24.04 vs. 171.60 ± 12.98, p < 0.001). After 1 year of follow-up, 61 patients (47.66%) with heart failure were readmitted to the hospital, including 8 deaths (13.11%). The AUC of the receiver operating characteristic (ROC) curve for the predictive value of FGF21 for prognosis was 0.964. Kaplan-Meier analysis results showed that there were significant differences in the 1-year mortality and heart failure readmission events between the grouped subjects. A poor prognosis was correlated with the serum level of FGF21, BNP, LVEDD, and LVEF, which was confirmed by the univariate Cox analysis. Conclusion FGF21 was independently associated with an increased risk of mortality and readmission HFrEF patients. Therefore, FGF21 has the potential to be a biomarker for the progression of HFrEF in patients.

Highlights

  • Heart failure (HF) is a serious clinical syndrome involving disorders of the autonomic, neuroendocrine, and immune systems

  • Serum levels of brain natriuretic peptide (BNP) and creatinine were significantly stronger in the patients with Heart Failure with reduced Ejection Fraction (HFrEF) than in controls

  • The concentration of fibroblast growth factor 21 (FGF21) was dramatically higher in the patients with HFrEF than in the control group (228:72 ± 24:04 vs. 171:60 ± 12:98, p < 0:001)

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Summary

Introduction

Heart failure (HF) is a serious clinical syndrome involving disorders of the autonomic, neuroendocrine, and immune systems. Improving risk prediction is of major importance in these patients [5, 6]. Biomarker detection is a critical approach to diagnose heart failure. This method usually detects the natriuretic peptides secreted mainly from myocardial cells in patients with heart failure due to pressure or volume overload [7, 8]. Factors such as obesity, age, renal function, and atrial fibrillation can affect brain natriuretic peptide (BNP) levels [9]. An objective biomarker with fewer interference factors is warranted

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