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Fibroblast growth factor 23-Klotho and mineral metabolism in the first year after pediatric kidney transplantation: A single-center prospective study

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PEDIATRIC TRANSPLANTATION
卷 -, 期 -, 页码 -

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WILEY
DOI: 10.1111/petr.14440

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FGF23; hypophosphatemia; pediatric kidney transplantation; klotho

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This study aimed to investigate the relationship between fibroblast growth factor 23 (FGF23) levels and mineral metabolism in pediatric kidney transplant patients. The results showed that FGF23 levels decreased rapidly after transplantation and were associated with hypophosphatemia and increased phosphorus excretion. Alpha Klotho levels were initially low but tended to increase after transplantation. Pre-transplant FGF23 and alpha Klotho were not significantly associated with post-transplant parameters.
BackgroundThe role of fibroblast growth factor 23 (FGF23) levels in mineral metabolism before and after kidney transplantation in pediatric patients is poorly understood. MethodsWe prospectively evaluated 24 patients under 18 years of age (4.5 [3.3-9.8] years) who underwent living kidney transplantation between July 2016 and March 2018, and measured intact FGF23 and serum alpha Klotho levels, and other parameters of mineral metabolism before and after transplantation (Day 7, 1 and 4 months, and 1 year). Relationships between parameters were examined by linear analysis. ResultsFGF23 level was 440.8 [63.4-5916.3] pg/ml pre-transplant and decreased significantly to 37.1 [16.0-71.5] pg/ml at Day 7 post-transplant (-91.6%, p < .001). Thereafter, it remained at normal levels until 1 year. alpha Klotho level was 785 [568-1292] pg/ml pre-transplant and remained low at Day 7 and 1 month post-transplant, with an increasing trend at 4 months. Post-transplant phosphorus levels were significantly decreased compared with pre-transplant, with a lowest level of 1.7 [1.3-2.9] mg/dl, -5.7 [-6.8, -3.8] SD at Day 4, followed by gradual recovery. Phosphorus levels and the ratio of tubular maximum phosphate reabsorption were significantly and negatively associated with pre-transplant FGF23 until 4 months of post-transplant. Pre-transplant alpha Klotho was negatively associated with pre-transplant FGF23 but not FGF23 or other parameters after transplantation. ConclusionFGF23 in pediatric kidney transplant patients decreased rapidly after transplantation and associated with post-transplant hypophosphatemia and increased phosphorus excretion. Post-transplant alpha Klotho was low early post-transplant but tended to increase subsequently. Post-transplant alpha Klotho was unaffected by pre-transplant FGF23 or other factors, suggesting pre-transplant chronic kidney disease status has no effect.

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