» Articles » PMID: 31175491

A Review of Fibroblast Growth Factor 21 in Diabetic Cardiomyopathy

Overview
Journal Heart Fail Rev
Date 2019 Jun 9
PMID 31175491
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

FGF21 (fibroblast growth factor 21) is a regulator of metabolism and performs an important role in glucose and lipid metabolism and the maintenance of energy balance. FGF21 is principally expressed in the liver, but it can also be found in the pancreas, skeletal muscle, and adipose tissue. It is known that levels of serum FGF21 are significantly elevated in obese, insulin-resistant patients, and those with metabolic syndrome. Elevated levels of FGF21 in serum during the early stages of various metabolic diseases are considered a compensatory response by the organism. Therefore, FGF21 is considered a hormone in response to stress and an early diagnostic marker of disease. Diabetic cardiomyopathy is a special type of cardiac complication, characterized as a chronic myocardial disorder caused by diabetes. The pathological process includes increased oxidative stress, energy metabolism in myocardial cells, an inflammatory response, and myocardial cell apoptosis. A growing body of evidence suggests that FGF21 has the potential to be an effective drug for the treatment of diabetic cardiomyopathy. Here, we review recent progress on the characteristics of FGF21 in its protective role, especially in pathological processes such as suppressing apoptosis in the myocardium, reducing inflammation in cardiomyocytes, reducing oxidative stress, and promoting fatty acid oxidation. In addition, we explore the possibility that diabetic cardiomyopathy can be delayed through the application of FGF21, providing possible therapeutic targets of the disease.

Citing Articles

Effects of exercise intensity and diet on cardiac tissue structure and FGF21/β-Klotho signaling in type 2 diabetic mice: a comparative study of HFD and HFD + STZ induced type 2 diabetes models in mice.

Moharamzadeh S, Kashef M, Salehpour M, Torabi M, Vesali S, Samsonchi Z Diabetol Metab Syndr. 2025; 17(1):4.

PMID: 39757236 PMC: 11702121. DOI: 10.1186/s13098-024-01541-3.


Predictive Value of NT-proBNP, FGF21, Galectin-3 and Copeptin in Advanced Heart Failure in Patients with Preserved and Mildly Reduced Ejection Fraction and Type 2 Diabetes Mellitus.

Ianos R, Iancu M, Pop C, Lucaciu R, Hangan A, Rahaian R Medicina (Kaunas). 2024; 60(11).

PMID: 39597026 PMC: 11596953. DOI: 10.3390/medicina60111841.


Role of Circulating Biomarkers in Diabetic Cardiomyopathy.

Ianos R, Cozma A, Lucaciu R, Hangan A, Negrean V, Mercea D Biomedicines. 2024; 12(9).

PMID: 39335666 PMC: 11428922. DOI: 10.3390/biomedicines12092153.


The role of nonmyocardial cells in the development of diabetic cardiomyopathy and the protective effects of FGF21: a current understanding.

Zhang T, Jiang D, Zhang X, Chen L, Jiang J, Zhang C Cell Commun Signal. 2024; 22(1):446.

PMID: 39327594 PMC: 11426003. DOI: 10.1186/s12964-024-01842-0.


Systemic impacts of metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) on heart, muscle, and kidney related diseases.

Sandireddy R, Sakthivel S, Gupta P, Behari J, Tripathi M, Singh B Front Cell Dev Biol. 2024; 12:1433857.

PMID: 39086662 PMC: 11289778. DOI: 10.3389/fcell.2024.1433857.


References
1.
Liu P, Su J, Song X, Wang S . Activation of nuclear β-catenin/c-Myc axis promotes oxidative stress injury in streptozotocin-induced diabetic cardiomyopathy. Biochem Biophys Res Commun. 2017; 493(4):1573-1580. DOI: 10.1016/j.bbrc.2017.10.027. View

2.
Yang H, Feng A, Lin S, Yu L, Lin X, Yan X . Fibroblast growth factor-21 prevents diabetic cardiomyopathy via AMPK-mediated antioxidation and lipid-lowering effects in the heart. Cell Death Dis. 2018; 9(2):227. PMC: 5833682. DOI: 10.1038/s41419-018-0307-5. View

3.
Jia G, Whaley-Connell A, Sowers J . Diabetic cardiomyopathy: a hyperglycaemia- and insulin-resistance-induced heart disease. Diabetologia. 2017; 61(1):21-28. PMC: 5720913. DOI: 10.1007/s00125-017-4390-4. View

4.
Staiger H, Keuper M, Berti L, de Angelis M, Haring H . Fibroblast Growth Factor 21-Metabolic Role in Mice and Men. Endocr Rev. 2017; 38(5):468-488. DOI: 10.1210/er.2017-00016. View

5.
Shiojima I, Walsh K . Regulation of cardiac growth and coronary angiogenesis by the Akt/PKB signaling pathway. Genes Dev. 2006; 20(24):3347-65. DOI: 10.1101/gad.1492806. View