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The Clinical Value of Klotho and FGF23 in Cardiac Valve Calcification Among Patients with Chronic Kidney Disease
Yan Chen1, Yan-Xia Chen1, Chong Huang1
1Department of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, People's Republic of China.
Insights
Serum Klotho and FGF23 levels are linked to cardiac valve calcification in chronic kidney disease (CKD) patients. Lower Glomerular Filtration Rate (GFR) correlates with increased FGF23 and decreased Klotho, both identified as independent risk factors.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Cardiac valve calcification is a common complication in patients with chronic kidney disease (CKD).
- The roles of serum Klotho and Fibroblast Growth Factor 23 (FGF23) in this process are not fully understood.
Purpose of the Study:
- To investigate the clinical significance of serum Klotho and FGF23 in predicting cardiac valve calcification among patients with varying stages of CKD.
- To identify independent risk factors for cardiac valve calcification in this population.
Main Methods:
- 180 patients with CKD were categorized into three groups based on disease stage (CKD2~3, CKD4, CKD5).
- Cardiac valve calcification was assessed using ultrasound.
- Logistic regression analysis was employed to determine independent risk factors.
Main Results:
- Serum FGF23 levels were inversely correlated with Glomerular Filtration Rate (GFR), increasing as GFR decreased.
- Serum Klotho levels showed a positive correlation with GFR, decreasing as GFR declined.
- Logistic regression identified GFR, serum creatinine, FGF23, and Klotho as independent risk factors for cardiac valve calcification.
Conclusions:
- Serum FGF23 and Klotho levels are significantly altered in CKD patients and are associated with cardiac valve calcification.
- GFR, serum creatinine, FGF23, and Klotho are key independent risk factors for cardiac valve calcification in CKD.
- These findings highlight the potential of FGF23 and Klotho as biomarkers for cardiovascular complications in CKD.
Objective:
This study aims to investigate the clinical value of serum Klotho and FGF23 in cardiac valve calcification in patients with chronic kidney disease (CKD).
Methods:
In the present study, 180 patients with CKD, who were admitted to the department of nephrology of our hospital on April 1, 2016 (solstice, 2019), were selected as the main subjects. According to the CKD stage, these patients were divided into three groups: CKD2~3 group, CKD4 group, and CKD5 group. In each group, ultrasound was used to evaluate the cardiac valve calcification, and the independent risk factors for cardiac valve calcification were analyzed by Logistic regression.
Results:
The levels of hemoglobin and blood calcium in CKD2~3 patients were higher than those in CKD4 and CKD5 patients, and the levels of hemoglobin and blood calcium in CKD5 patients were higher than those in CKD4 patients (P<0.05). Albumin was lower in CKD2~3 patients when compared to CKD5 patients while albumin was higher in CKD5 patients when compared to CKD4 patients (P<0.05). The serum levels of FGF23 was lower in CKD2~3 patients when compared to CKD4 and CKD5 patients while the serum levels of FGF23 was lower in CKD4 patients when compared to CKD5 patients (P<0.05). The serum levels of Klotho was higher in CKD2~3 patients, when compared to CKD4 and CKD5 patients, while the serum levels of Klotho was higher in CKD4 patients, when compared to CKD5 patients (P<0.05). The logistic regression analysis revealed that GFR, serum creatinine, FGF23 and Klotho were independent risk factors for cardiac valve calcification in patients with CKD.
Conclusion:
With the decrease of GFR in CKD patients, the serum levels of FGF23 increases, while the serum levels of Klotho decreases. Furthermore, the serum levels of FGF23 and Klotho are affected by various factors, and the levels of FGF23 and Klotho in CKD patients are negatively correlated. GFR, serum creatinine, FGF23 and Klotho are independent risk factors for heart valve calcification in patients with CKD.
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