The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis

Fibroblast growth factor 23 (FGF23) is a phosphotropic hormone secreted by osteoblasts and osteocytes into the systemic circulation. It exerts its effects on the kidneys, parathyroid glands, heart, and bones. FGF23 is a critical phosphaturic hormone that, alongside parathyroid hormone (PTH), regula...

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Main Authors: Vladyslav Bardash, Tetiana Maksymets, Eugen Sklyarov
Format: Article
Language:English
Published: National Kidney Foundation of Ukraine 2025-06-01
Series:Український Журнал Нефрології та Діалізу
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Online Access:https://ukrjnd.com.ua/index.php/journal/article/view/941
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author Vladyslav Bardash
Tetiana Maksymets
Eugen Sklyarov
author_facet Vladyslav Bardash
Tetiana Maksymets
Eugen Sklyarov
author_sort Vladyslav Bardash
collection DOAJ
description Fibroblast growth factor 23 (FGF23) is a phosphotropic hormone secreted by osteoblasts and osteocytes into the systemic circulation. It exerts its effects on the kidneys, parathyroid glands, heart, and bones. FGF23 is a critical phosphaturic hormone that, alongside parathyroid hormone (PTH), regulates phosphate reabsorption and calcitriol (1,25(OH)₂D) synthesis in the kidneys. The present study aimed to evaluate the diagnostic and prognostic significance of fibroblast growth factor 23 in patients undergoing hemodialysis. Methods. A total of 88 patients were examined in this cross-sectional study. The cohort comprised 36 women (40.9%; 95% CI 30.64–51.18) and 52 men (59.1%; 95% CI 48.82–69.36), with a mean age of 55.81 ± 13.14 years. Group 1 consisted of 69 patients with stage 5 chronic kidney disease (CKD) receiving renal replacement therapy via hemodialysis, while Group 2 included 19 patients with stage 3 CKD. Results. FGF23 levels were elevated in 67 patients (97.1%; 95% CI 91.87–99.72) in Group 1, with a median (Me) of 1258.32 pg/mL (interquartile range [IQR] 169.46–1338.46). In Group 2, FGF23 levels were elevated in 18 patients (94.7%; 95% CI 80.58–100), with a median of 150.5 pg/mL (IQR 74.22–929.12). A significant difference was observed between the groups (p < 0.05). The median duration of hemodialysis in Group 1 was 15 months (IQR 8–36). In Group 1, correlation analysis revealed weak associations between FGF23 and phosphorus (r = 0.13; p > 0.05), total calcium (r = 0.04; p < 0.05), ionized calcium (r = 0.02; p < 0.05), and parathyroid hormone (r = 0.08; p > 0.05). Significant correlations were found between FGF23 and creatinine (r = 0.41; p < 0.005), urea (r = 0.33; p < 0.005), urine volume (r = -0.75; p < 0.005), and hemodialysis duration (r = 0.57; p < 0.005). Regression analysis for predicting residual urine volume based on FGF23, creatinine, urea, and hemodialysis duration yielded an R² of 0.7369, F-statistic of 92.45 (p < 0.0001), standard error of residuals of 5.843, and residual degrees of freedom of 66. Conclusions. The weak correlations between FGF23 and calcium-phosphorus metabolism indicate that FGF23 is not a suitable diagnostic marker for mineral and bone disorders (CKD-MBD) in patients undergoing hemodialysis. However, FGF23 is a significant predictor of residual urine volume in hemodialysis patients, as demonstrated by the regression analysis. The model, incorporating FGF23 and hemodialysis duration, explains 73.7% of the variation in urine volume, highlighting its strong prognostic capability. These findings underscore the clinical significance of FGF23 as a biomarker for assessing residual renal function in dialysis patients.
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spelling doaj-art-582c0def97e64c6dadc91eaba97baea52025-08-20T03:20:44ZengNational Kidney Foundation of UkraineУкраїнський Журнал Нефрології та Діалізу2304-02382616-73522025-06-012(86)10.31450/ukrjnd.2(86).2025.05The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysisVladyslav Bardash0Tetiana Maksymets1Eugen Sklyarov2Danylo Halytsky Lviv National Medical University, Lviv, UkraineDanylo Halytsky Lviv National Medical University, Lviv, UkraineDanylo Halytsky Lviv National Medical University, Lviv, Ukraine Fibroblast growth factor 23 (FGF23) is a phosphotropic hormone secreted by osteoblasts and osteocytes into the systemic circulation. It exerts its effects on the kidneys, parathyroid glands, heart, and bones. FGF23 is a critical phosphaturic hormone that, alongside parathyroid hormone (PTH), regulates phosphate reabsorption and calcitriol (1,25(OH)₂D) synthesis in the kidneys. The present study aimed to evaluate the diagnostic and prognostic significance of fibroblast growth factor 23 in patients undergoing hemodialysis. Methods. A total of 88 patients were examined in this cross-sectional study. The cohort comprised 36 women (40.9%; 95% CI 30.64–51.18) and 52 men (59.1%; 95% CI 48.82–69.36), with a mean age of 55.81 ± 13.14 years. Group 1 consisted of 69 patients with stage 5 chronic kidney disease (CKD) receiving renal replacement therapy via hemodialysis, while Group 2 included 19 patients with stage 3 CKD. Results. FGF23 levels were elevated in 67 patients (97.1%; 95% CI 91.87–99.72) in Group 1, with a median (Me) of 1258.32 pg/mL (interquartile range [IQR] 169.46–1338.46). In Group 2, FGF23 levels were elevated in 18 patients (94.7%; 95% CI 80.58–100), with a median of 150.5 pg/mL (IQR 74.22–929.12). A significant difference was observed between the groups (p < 0.05). The median duration of hemodialysis in Group 1 was 15 months (IQR 8–36). In Group 1, correlation analysis revealed weak associations between FGF23 and phosphorus (r = 0.13; p > 0.05), total calcium (r = 0.04; p < 0.05), ionized calcium (r = 0.02; p < 0.05), and parathyroid hormone (r = 0.08; p > 0.05). Significant correlations were found between FGF23 and creatinine (r = 0.41; p < 0.005), urea (r = 0.33; p < 0.005), urine volume (r = -0.75; p < 0.005), and hemodialysis duration (r = 0.57; p < 0.005). Regression analysis for predicting residual urine volume based on FGF23, creatinine, urea, and hemodialysis duration yielded an R² of 0.7369, F-statistic of 92.45 (p < 0.0001), standard error of residuals of 5.843, and residual degrees of freedom of 66. Conclusions. The weak correlations between FGF23 and calcium-phosphorus metabolism indicate that FGF23 is not a suitable diagnostic marker for mineral and bone disorders (CKD-MBD) in patients undergoing hemodialysis. However, FGF23 is a significant predictor of residual urine volume in hemodialysis patients, as demonstrated by the regression analysis. The model, incorporating FGF23 and hemodialysis duration, explains 73.7% of the variation in urine volume, highlighting its strong prognostic capability. These findings underscore the clinical significance of FGF23 as a biomarker for assessing residual renal function in dialysis patients. https://ukrjnd.com.ua/index.php/journal/article/view/941fibroblast growth factor 23, chronic kidney disease, hemodialysis, calcium-phosphate metabolism, diuresis.
spellingShingle Vladyslav Bardash
Tetiana Maksymets
Eugen Sklyarov
The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
Український Журнал Нефрології та Діалізу
fibroblast growth factor 23, chronic kidney disease, hemodialysis, calcium-phosphate metabolism, diuresis.
title The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
title_full The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
title_fullStr The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
title_full_unstemmed The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
title_short The prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
title_sort prognostic and diagnostic value of fibroblast growth factor 23 in patients undergoing hemodialysis
topic fibroblast growth factor 23, chronic kidney disease, hemodialysis, calcium-phosphate metabolism, diuresis.
url https://ukrjnd.com.ua/index.php/journal/article/view/941
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