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Updated: Oct 31, 2025

A Semi-Automated and Reproducible Biological-Based Method to Quantify Calcium Deposition In Vitro
Published on: June 2, 2022
Fibroblast Growth Factor 21 Predicts and Promotes Vascular Calcification in Haemodialysis Patients
Liqiong Jiang1,2, Qing Yin1, Min Yang3
1Institute of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Insights
Fibroblast growth factor 21 (FGF21) is significantly elevated in hemodialysis patients and strongly predicts vascular calcification (VC). FGF21 also promotes VC by increasing calcium deposition and endothelial-to-mesenchymal transition.
Area of Science:
- Endocrinology
- Nephrology
- Cardiovascular Medicine
Background:
- Cardiovascular disease (CVD) is the primary cause of mortality in hemodialysis (HD) patients.
- Vascular calcification (VC) is accelerated in HD patients, correlating with CVD events and mortality.
- Fibroblast growth factor 21 (FGF21) is a novel hypoglycemic adipocytokine inversely related to bone mineral density.
Purpose of the Study:
- To investigate the association between FGF21 and vascular calcification (VC) in hemodialysis (HD) patients.
- To evaluate FGF21's role in promoting VC in vitro.
Main Methods:
- Cross-sectional study measuring serum FGF21 and thoracic aorta calcification scores (TACS) in HD patients.
- In vitro experiments using human aortic endothelial cells (HAECs) treated with FGF21 and parathyroid hormone (PTH).
Main Results:
- HD patients exhibited 11-fold higher FGF21 levels than controls.
- Serum FGF21 positively correlated with TACS and its segments (ATACS, AoACS, DTACS) and was an independent predictor of VC.
- FGF21, combined with age, calcium, and PTH, achieved high predictive value for VC (AUC 0.84).
- In vitro, FGF21 enhanced PTH-induced calcification in HAECs via increased calcium deposition and endothelial-to-mesenchymal transition.
Conclusions:
- Elevated circulating FGF21 is a significant finding in HD patients.
- FGF21 acts as a potential predictor and promoter of vascular calcification in HD patients.
Background:
Cardiovascular disease (CVD) is the leading cause of death in haemodialysis (HD) patients. Vascular calcification (VC) is dramatically accelerated and is strongly associated with CVD events and mortality in HD patients. VC coexists with osteoporosis in many studies. Fibroblast growth factor 21 (FGF21) which is known as an adipocytokine is a new hypoglycemic strategy and is inversely related to bone mineral density.
Methods:
To evaluate the contribution of FGF21 to VC in HD patients, we detected circulating FGF21 levels and measured the whole thoracic aorta calcification scores (TACS) and calcification scores of the 3 segments of thoracic aorta, including ascending thoracic aorta (ATACS), aortic arch (AoACS), and descending thoracic aorta (DTACS) of our HD patients in this cross-sectional study. In addition, we pre-incubated human aortic endothelial cells (HAECs) with FGF21 in the presence or absence of parathyroid hormone (PTH) in vitro.
Results:
The median serum FGF21 level in HD patients was 11-fold higher than that in healthy controls. Ln(FGF21) was positively correlated with Ln(TACS+1), Ln(ATACS+1), Ln(AoACS+1), and Ln(DTACS+1), respectively, in HD patients. Serum FGF21 was independently associated with TACS and ATACS, AoACS, and DTACS. FGF21 which was combined with age, calcium, and intact PTH demonstrated a high area under the curve of 0.84 with optimal sensitivity (84%) and specificity (71%) for the prediction of VC in HD patients. Our vitro results showed that FGF21 enhanced the calcification effect of PTH on HAECs by increasing calcium deposition and endothelial-to-mesenchymal transition.
Conclusions:
Circulating FGF21 was notably higher and was a potential predictor and promoter of VC in HD patients.
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