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Urinary Fibroblast Growth Factor-23 and Soluble Alpha-Klotho in Cats with Chronic Kidney Disease
Wei-Che Chen1, Wei-Li Hsu2, Chao-Chin Chang2
1Institute of Veterinary Clinical Science, School of Veterinary Medicine, College of Bio-Resources and Agriculture, National Taiwan University, Taipei, Taiwan; National Taiwan University Veterinary Hospital, College of Bio-Resources and Agriculture, National Taiwan University, Taipei, Taiwan.
Insights
Urinary Fibroblast growth factor 23 (FGF23) and α-Klotho (KL) levels increase with feline chronic kidney disease (CKD) progression. Lower urinary KL is a key predictor of CKD advancement in cats.
Area of Science:
- Veterinary Medicine
- Nephrology
- Biochemistry
Background:
- Fibroblast growth factor 23 (FGF23) and α-Klotho (KL) are critical regulators of mineral and bone metabolism.
- Their roles in feline chronic kidney disease-mineral and bone disorder (CKD-MBD) are not well understood due to limited urinary studies.
- Understanding these biomarkers is essential for managing feline CKD progression.
Purpose of the Study:
- To evaluate urinary FGF23 (uFGF23) and soluble α-Klotho (uKL) concentrations in cats with varying stages of CKD.
- To assess the relationship between uFGF23, uKL, and CKD progression, including acute decompensated chronic kidney disease (ACKD).
- To identify potential urinary biomarkers for feline CKD assessment and prognosis.
Main Methods:
- Quantification of uFGF23 and uKL using commercial ELISA kits.
- Analysis of samples from 13 healthy cats, 71 CKD cats, and 28 ACKD cats.
- Statistical analysis to compare biomarker levels across groups and assess prognostic value.
Main Results:
- The urinary FGF23-to-creatinine ratio was significantly elevated in late-stage CKD and ACKD cats compared to healthy and early CKD cats.
- A progressive decline in the urinary Klotho/FGF23 ratio was observed from healthy to late-stage CKD cats.
- Lower levels of urinary Klotho were identified as an independent predictor of CKD progression in cats.
Conclusions:
- Urinary FGF23 and Klotho levels, along with their ratio, show significant alterations with feline CKD progression.
- These urinary biomarkers may serve as valuable tools for assessing the severity of CKD in cats.
- Urinary Klotho levels show prognostic potential for predicting CKD progression in feline patients.
Abstract:
Fibroblast growth factor 23 (FGF23) and α-Klotho play crucial roles in the pathogenesis of chronic kidney disease-mineral and bone disorder (CKD-MBD) due to their regulatory effects on phosphorus, calcium, parathyroid hormone, and calcitriol levels. Despite their importance, few studies have examined urinary concentrations of these compounds in feline chronic kidney disease (CKD), thereby limiting our understanding of their roles in disease progression. This study aimed to evaluate the urinary levels of FGF23 (uFGF23) and soluble α-Klotho (uKL) in cats at various stages of CKD, including acute decompensated chronic kidney disease (ACKD), and to assess their respective relationship with disease progression. We quantified these levels using commercial ELISA kits in a cohort of 13 healthy cats, 71 CKD cats, and 28 ACKD cats. Our results revealed a significant elevation of uFGF23-to-urine-creatinine ratio with late CKD (median: 7.08 ×10-7) and ACKD (10.9 ×10-7) cats compared to early CKD cats (2.91 ×10-7, p = 0.005 and p < 0.001, respectively) and healthy cats (0.86 ×10-7, p < 0.001 in both comparisons). The urinary Klotho/FGF23 ratio exhibited a progressive decline from healthy cats (0.144) to early-stage CKD cats (0.108, p = 0.014), and thence to late-stage CKD cats (0.094, p = 0.039). Lower tertiles of uKL levels were identified as an independent prognostic factor for CKD progression (hazard ratio: 8.49, p = 0.004). In conclusion, these findings suggest that uFGF23, uKL, and their ratio may serve as useful biomarkers for assessing CKD and predicting CKD progression in cats.
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