4.4 Article

Fibroblast growth factor 21 in heart failure

Journal

HEART FAILURE REVIEWS
Volume 28, Issue 1, Pages 261-272

Publisher

SPRINGER
DOI: 10.1007/s10741-022-10268-0

Keywords

Biomarker; Cardiomyocyte; Fibroblast growth factor 21; Heart failure

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Fibroblast growth factor 21 (FGF21) is a hormone involved in energy regulation and has been shown to protect against obesity and diabetes. However, its role in heart failure (HF) is not well understood. HF is a global health problem with a rising prevalence, especially in aging populations. The emergence of cardiac biomarkers has been of great interest in improving prediction, diagnosis, and prognosis of HF. Recent studies suggest that FGF21 may be a promising biomarker for HF, but there are conflicting findings in clinical literature. Further research is needed to understand the causal role of FGF21 in HF and its potential as a biomarker for prediction, diagnosis, and prognosis.
Fibroblast growth factor 21 (FGF21) is a peptide hormone involved in energy homeostasis that protects against the development of obesity and diabetes in animal models. Its level is elevated in atherosclerotic cardiovascular diseases (CVD) in humans. However, little is known about the role of FGF21 in heart failure (HF). HF is a major global health problem with a prevalence that is predicted to rise, especially in ageing populations. Despite improved therapies, mortality due to HF remains high, and given its insidious onset, prediction of its development is challenging for physicians. The emergence of cardiac biomarkers to improve prediction, diagnosis, and prognosis of HF has received much attention over the past decade. Recent studies have suggested FGF21 is a promising biomarker candidate for HF. Preclinical research has shown that FGF21 is involved in the pathophysiology of HF through the prevention of oxidative stress, cardiac hypertrophy, and inflammation in cardiomyocytes. However, in the available clinical literature, FGF21 levels appear to be paradoxically raised in HF, potentially implying a FGF21 resistant state as occurs in obesity. Several potential confounding variables complicate the verdict on whether FGF21 is of clinical value as a biomarker. Further research is thus needed to evaluate whether FGF21 has a causal role in HF, and whether circulating FGF21 can be used as a biomarker to improve the prediction, diagnosis, and prognosis of HF. This review draws from preclinical and clinical studies to explore the role of FGF21 in HF.

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