Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients

Background. Chronic kidney disease (CKD) related mineral bone disorders persist after kidney transplantation, but little is known about the relationship between fibroblast growth factor-23 (FGF-23) and mineral metabolism in prevalent post-transplant patients. Objectives. To examine mineral metabolis...

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Main Authors: Madhumathi Rao, Priyanka Jain, Temitope Ojo, Gautam Surya, Vaidyanathapuram Balakrishnan
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Nephrology
Online Access:http://dx.doi.org/10.1155/2012/490623
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author Madhumathi Rao
Priyanka Jain
Temitope Ojo
Gautam Surya
Vaidyanathapuram Balakrishnan
author_facet Madhumathi Rao
Priyanka Jain
Temitope Ojo
Gautam Surya
Vaidyanathapuram Balakrishnan
author_sort Madhumathi Rao
collection DOAJ
description Background. Chronic kidney disease (CKD) related mineral bone disorders persist after kidney transplantation, but little is known about the relationship between fibroblast growth factor-23 (FGF-23) and mineral metabolism in prevalent post-transplant patients. Objectives. To examine mineral metabolism parameters and their relationship to FGF-23 and parathyroid hormone (PTH) in prevalent kidney transplant patients. Methods. Cross-sectional study of 106 kidney transplant patients enrolled November 2005–October 2009 at Tufts Medical Center (TMC), Boston. Results. The prevalence of hypophosphatemia was 34%, hypercalcemia 3%, and elevated PTH levels 66%, at a median (25th–75th percentile) duration of 12.8 (7.5–30.9) months post-transplant. Males had significantly higher levels of PTH (P=0.04) and lower levels of serum phosphate (P=0.002). Serum PTH levels did not relate to eGFR, corrected calcium levels or serum phosphate. FGF-23 levels were above the reference limits in 7% of patients; higher levels were associated with higher serum phosphate and PTH levels after adjustment for transplant kidney function. Conclusion. FGF-23 is an important driver of mineral metabolism in prevalent transplant patients. Its modulatory role in mineral metabolism homeostasis may be heightened as feedback suppression of PTH is disturbed. Its role in long term cardiovascular and graft outcomes needs further study.
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spelling doaj-art-fd548e4ba71a46b5ac5a5a5bfd5b48412025-02-03T05:57:39ZengWileyInternational Journal of Nephrology2090-214X2090-21582012-01-01201210.1155/2012/490623490623Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant PatientsMadhumathi Rao0Priyanka Jain1Temitope Ojo2Gautam Surya3Vaidyanathapuram Balakrishnan4Division of Nephrology, Tufts Medical Center, P.O. Box 391, 800 Washington Street, Boston, MA 02111, USADivision of Nephrology, Tufts Medical Center, P.O. Box 391, 800 Washington Street, Boston, MA 02111, USADivision of Nephrology, Tufts Medical Center, P.O. Box 391, 800 Washington Street, Boston, MA 02111, USADivision of Nephrology, Tufts Medical Center, P.O. Box 391, 800 Washington Street, Boston, MA 02111, USADivision of Nephrology, Tufts Medical Center, P.O. Box 391, 800 Washington Street, Boston, MA 02111, USABackground. Chronic kidney disease (CKD) related mineral bone disorders persist after kidney transplantation, but little is known about the relationship between fibroblast growth factor-23 (FGF-23) and mineral metabolism in prevalent post-transplant patients. Objectives. To examine mineral metabolism parameters and their relationship to FGF-23 and parathyroid hormone (PTH) in prevalent kidney transplant patients. Methods. Cross-sectional study of 106 kidney transplant patients enrolled November 2005–October 2009 at Tufts Medical Center (TMC), Boston. Results. The prevalence of hypophosphatemia was 34%, hypercalcemia 3%, and elevated PTH levels 66%, at a median (25th–75th percentile) duration of 12.8 (7.5–30.9) months post-transplant. Males had significantly higher levels of PTH (P=0.04) and lower levels of serum phosphate (P=0.002). Serum PTH levels did not relate to eGFR, corrected calcium levels or serum phosphate. FGF-23 levels were above the reference limits in 7% of patients; higher levels were associated with higher serum phosphate and PTH levels after adjustment for transplant kidney function. Conclusion. FGF-23 is an important driver of mineral metabolism in prevalent transplant patients. Its modulatory role in mineral metabolism homeostasis may be heightened as feedback suppression of PTH is disturbed. Its role in long term cardiovascular and graft outcomes needs further study.http://dx.doi.org/10.1155/2012/490623
spellingShingle Madhumathi Rao
Priyanka Jain
Temitope Ojo
Gautam Surya
Vaidyanathapuram Balakrishnan
Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
International Journal of Nephrology
title Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
title_full Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
title_fullStr Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
title_full_unstemmed Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
title_short Fibroblast Growth Factor and Mineral Metabolism Parameters among Prevalent Kidney Transplant Patients
title_sort fibroblast growth factor and mineral metabolism parameters among prevalent kidney transplant patients
url http://dx.doi.org/10.1155/2012/490623
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AT temitopeojo fibroblastgrowthfactorandmineralmetabolismparametersamongprevalentkidneytransplantpatients
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