» Articles » PMID: 30185439

Circulating Level of Fibroblast Growth Factor 21 is Independently Associated with the Risks of Unstable Angina Pectoris

Overview
Journal Biosci Rep
Specialty Cell Biology
Date 2018 Sep 7
PMID 30185439
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

There is increasing evidence that serum adipokine levels are associated with higher risks of cardiovascular diseases. As an important adipokine, fibroblast growth factor 21 (FGF21) has been demonstrated to be associated with atherosclerosis and coronary artery disease (CAD). However, circulating level of FGF21 in patients with angina pectoris has not yet been investigated. Circulating FGF21 level was examined in 197 patients with stable angina pectoris (SAP, =66), unstable angina pectoris (UAP, =76), and control subjects (=55) along with clinical variables of cardiovascular risk factors. Serum FGF21 concentrations on admission were significantly increased more in patients with UAP than those with SAP (Ln-FGF21: 5.26 ± 0.87 compared with 4.85 ± 0.77, <0.05) and control subjects (natural logarithm (Ln)-FGF21: 5.26 ± 0.87 compared with 4.54 ± 0.72, <0.01). The correlation analysis revealed that serum FGF21 concentration was positively correlated with the levels of cardiac troponin I (cTnI) (r  =  0.026, =0.027) and creatine kinase-MB (CK-MB) (r  =  0.023, = 0.04). Furthermore, FGF21 level was identified as an independent factor associated with the risks of UAP (odds ratio (OR): 2.781; 95% CI: 1.476-5.239; 0.002), after adjusting for gender, age, and body mass index (BMI). However, there were no correlations between serum FGF21 levels and the presence of SAP (OR: 1.248; 95% CI: 0.703-2.215; 0.448). The present study indicates that FGF21 has a strong correlation and precise predictability for increased risks of UAP, that is independent of traditional risk factors of angina pectoris.

Citing Articles

Can Exercise-Mediated Adipose Browning Provide an Alternative Explanation for the Obesity Paradox?.

Zhao J, Li X, Liang C, Yan Y Int J Mol Sci. 2025; 26(5).

PMID: 40076419 PMC: 11898606. DOI: 10.3390/ijms26051790.


Connecting the Dots: FGF21 as a Potential Link between Obesity and Cardiovascular Health in Acute Coronary Syndrome Patients.

Negroiu C, Riza A, Streata I, Tudorascu I, Bezna C, Ungureanu A Curr Issues Mol Biol. 2024; 46(8):8512-8525.

PMID: 39194718 PMC: 11353113. DOI: 10.3390/cimb46080501.


The Correlation Between Serum Fibroblast Growth Factor 21 and the Severity and Occurrence of Coronary Artery Disease.

Sinha S, Prakash P, Keshari J, Prasad R Cureus. 2024; 16(1):e51924.

PMID: 38333506 PMC: 10851179. DOI: 10.7759/cureus.51924.


Elevated serum FGF21 is an independent predictor for adverse events in hemodialysis patients from two large centers: a prospective cohort study.

Li M, Jiang L, Zhang M, Liu S, Sawh R, Zheng J Ren Fail. 2023; 45(2):2256414.

PMID: 37724523 PMC: 10512844. DOI: 10.1080/0886022X.2023.2256414.


Targeting FGF21 in cardiovascular and metabolic diseases: from mechanism to medicine.

Tan H, Yue T, Chen Z, Wu W, Xu S, Weng J Int J Biol Sci. 2023; 19(1):66-88.

PMID: 36594101 PMC: 9760446. DOI: 10.7150/ijbs.73936.


References
1.
Patel V, Adya R, Chen J, Ramanjaneya M, Bari M, Bhudia S . Novel insights into the cardio-protective effects of FGF21 in lean and obese rat hearts. PLoS One. 2014; 9(2):e87102. PMC: 3911936. DOI: 10.1371/journal.pone.0087102. View

2.
Yan H, Xia M, Chang X, Xu Q, Bian H, Zeng M . Circulating fibroblast growth factor 21 levels are closely associated with hepatic fat content: a cross-sectional study. PLoS One. 2011; 6(9):e24895. PMC: 3174975. DOI: 10.1371/journal.pone.0024895. View

3.
Cheng X, Zhu B, Jiang F, Fan H . Serum FGF-21 levels in type 2 diabetic patients. Endocr Res. 2011; 36(4):142-8. DOI: 10.3109/07435800.2011.558550. View

4.
Stefan N, Haring H . The role of hepatokines in metabolism. Nat Rev Endocrinol. 2013; 9(3):144-52. DOI: 10.1038/nrendo.2012.258. View

5.
Wang J, Sheu W, Lee W, Lee I, Lin S, Lee W . Associations of fibroblast growth factor 21 with cardiovascular risk and β-cell function in patients who had no history of diabetes. Clin Chim Acta. 2017; 472:80-85. DOI: 10.1016/j.cca.2017.07.017. View