Fibroblast growth factor 23 and calcium phosphate homeostasis after pediatric renal transplantation.

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Fibroblast growth factor 23 and calcium phosphate homeostasis after pediatric renal transplantation. / Van Husen, Michel; Lehnhardt, Anja; Fischer, Ann-Katrin; Brinkert, Florian; Loos, Sebastian; Oh, Jun; Kemper, Markus J.

In: PEDIATR TRANSPLANT, Vol. 16, No. 5, 5, 2012, p. 443-450.

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@article{32dce7b6821949cca1b42a80d1679c55,
title = "Fibroblast growth factor 23 and calcium phosphate homeostasis after pediatric renal transplantation.",
abstract = "FGF23 is a circulating factor regulating TPR and is increased in CKD. After RT, it seems to induce phosphorus wasting in adults. Data on FGF23 after PRT are scarce. Parameters of bone metabolism including calcium, phosphate, 25-(OH) vitamin D, 1,25-(OH)(2) vitamin D, alkaline phosphatase, PTH, and FGF23 were analyzed in 57 children after PRT and 11 controls. Median time after PRT was 25.9 (range 2-135) months. eGFR after PRT ranged from 15 to 175 mL/min/1.73 qm. Mean (±s.e.) FGF23 and PTH levels were significantly elevated compared with controls (146 ± 30 vs. 43 ± 3 ng/L, p = 0.001 and 182 ± 42 vs. 74 ± 18 ng/L, p = 0.004, respectively). Highest FGF23 levels were found in children with an eGFR below 60 mL/min*1.73 sqm (280 ± 69 vs. 62 ± 5 ng/L, p = 0.001), but significantly elevated values were already present in CKD2T. In a multivariate analysis, eGFR, PTH, calcium, and phosphate were significantly associated with FGF23. In a subgroup of 17 patients (29.8%) with persistent hypophosphatemia, phosphate levels were significantly associated with FGF23 and not with PTH. FGF23 is increased in children after PRT, especially in patients with chronic allograft dysfunction, and seems to be a more sensitive marker of dysregulated calcium phosphate homeostasis than PTH.",
keywords = "Humans, Male, Female, Adolescent, Multivariate Analysis, Treatment Outcome, Child, Cross-Sectional Studies, Child, Preschool, Infant, Case-Control Studies, Biological Markers/blood, *Kidney Transplantation, Calcium Phosphates/*blood, Fibroblast Growth Factors/*blood, *Homeostasis, Hypophosphatemia/blood/etiology, Kidney Failure, Chronic/blood/*surgery, Parathyroid Hormone/blood, Postoperative Complications/blood, Vitamin D/analogs & derivatives/blood, Humans, Male, Female, Adolescent, Multivariate Analysis, Treatment Outcome, Child, Cross-Sectional Studies, Child, Preschool, Infant, Case-Control Studies, Biological Markers/blood, *Kidney Transplantation, Calcium Phosphates/*blood, Fibroblast Growth Factors/*blood, *Homeostasis, Hypophosphatemia/blood/etiology, Kidney Failure, Chronic/blood/*surgery, Parathyroid Hormone/blood, Postoperative Complications/blood, Vitamin D/analogs & derivatives/blood",
author = "{Van Husen}, Michel and Anja Lehnhardt and Ann-Katrin Fischer and Florian Brinkert and Sebastian Loos and Jun Oh and Kemper, {Markus J.}",
year = "2012",
language = "English",
volume = "16",
pages = "443--450",
journal = "PEDIATR TRANSPLANT",
issn = "1397-3142",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Fibroblast growth factor 23 and calcium phosphate homeostasis after pediatric renal transplantation.

AU - Van Husen, Michel

AU - Lehnhardt, Anja

AU - Fischer, Ann-Katrin

AU - Brinkert, Florian

AU - Loos, Sebastian

AU - Oh, Jun

AU - Kemper, Markus J.

PY - 2012

Y1 - 2012

N2 - FGF23 is a circulating factor regulating TPR and is increased in CKD. After RT, it seems to induce phosphorus wasting in adults. Data on FGF23 after PRT are scarce. Parameters of bone metabolism including calcium, phosphate, 25-(OH) vitamin D, 1,25-(OH)(2) vitamin D, alkaline phosphatase, PTH, and FGF23 were analyzed in 57 children after PRT and 11 controls. Median time after PRT was 25.9 (range 2-135) months. eGFR after PRT ranged from 15 to 175 mL/min/1.73 qm. Mean (±s.e.) FGF23 and PTH levels were significantly elevated compared with controls (146 ± 30 vs. 43 ± 3 ng/L, p = 0.001 and 182 ± 42 vs. 74 ± 18 ng/L, p = 0.004, respectively). Highest FGF23 levels were found in children with an eGFR below 60 mL/min*1.73 sqm (280 ± 69 vs. 62 ± 5 ng/L, p = 0.001), but significantly elevated values were already present in CKD2T. In a multivariate analysis, eGFR, PTH, calcium, and phosphate were significantly associated with FGF23. In a subgroup of 17 patients (29.8%) with persistent hypophosphatemia, phosphate levels were significantly associated with FGF23 and not with PTH. FGF23 is increased in children after PRT, especially in patients with chronic allograft dysfunction, and seems to be a more sensitive marker of dysregulated calcium phosphate homeostasis than PTH.

AB - FGF23 is a circulating factor regulating TPR and is increased in CKD. After RT, it seems to induce phosphorus wasting in adults. Data on FGF23 after PRT are scarce. Parameters of bone metabolism including calcium, phosphate, 25-(OH) vitamin D, 1,25-(OH)(2) vitamin D, alkaline phosphatase, PTH, and FGF23 were analyzed in 57 children after PRT and 11 controls. Median time after PRT was 25.9 (range 2-135) months. eGFR after PRT ranged from 15 to 175 mL/min/1.73 qm. Mean (±s.e.) FGF23 and PTH levels were significantly elevated compared with controls (146 ± 30 vs. 43 ± 3 ng/L, p = 0.001 and 182 ± 42 vs. 74 ± 18 ng/L, p = 0.004, respectively). Highest FGF23 levels were found in children with an eGFR below 60 mL/min*1.73 sqm (280 ± 69 vs. 62 ± 5 ng/L, p = 0.001), but significantly elevated values were already present in CKD2T. In a multivariate analysis, eGFR, PTH, calcium, and phosphate were significantly associated with FGF23. In a subgroup of 17 patients (29.8%) with persistent hypophosphatemia, phosphate levels were significantly associated with FGF23 and not with PTH. FGF23 is increased in children after PRT, especially in patients with chronic allograft dysfunction, and seems to be a more sensitive marker of dysregulated calcium phosphate homeostasis than PTH.

KW - Humans

KW - Male

KW - Female

KW - Adolescent

KW - Multivariate Analysis

KW - Treatment Outcome

KW - Child

KW - Cross-Sectional Studies

KW - Child, Preschool

KW - Infant

KW - Case-Control Studies

KW - Biological Markers/blood

KW - Kidney Transplantation

KW - Calcium Phosphates/blood

KW - Fibroblast Growth Factors/blood

KW - Homeostasis

KW - Hypophosphatemia/blood/etiology

KW - Kidney Failure, Chronic/blood/surgery

KW - Parathyroid Hormone/blood

KW - Postoperative Complications/blood

KW - Vitamin D/analogs & derivatives/blood

KW - Humans

KW - Male

KW - Female

KW - Adolescent

KW - Multivariate Analysis

KW - Treatment Outcome

KW - Child

KW - Cross-Sectional Studies

KW - Child, Preschool

KW - Infant

KW - Case-Control Studies

KW - Biological Markers/blood

KW - Kidney Transplantation

KW - Calcium Phosphates/blood

KW - Fibroblast Growth Factors/blood

KW - Homeostasis

KW - Hypophosphatemia/blood/etiology

KW - Kidney Failure, Chronic/blood/surgery

KW - Parathyroid Hormone/blood

KW - Postoperative Complications/blood

KW - Vitamin D/analogs & derivatives/blood

M3 - SCORING: Journal article

VL - 16

SP - 443

EP - 450

JO - PEDIATR TRANSPLANT

JF - PEDIATR TRANSPLANT

SN - 1397-3142

IS - 5

M1 - 5

ER -