학술논문

Regulation of fibroblast growth factor-23 in chronic kidney disease.
Document Type
Article
Source
Nephrology Dialysis Transplantation. Nov2007, Vol. 22 Issue 11, p3202-3202. 1p.
Subject
*GROWTH factors
*FIBROBLAST growth factors
*MITOGENS
*CYTOKINES
Language
ISSN
0931-0509
Abstract
Background. Fibroblast growth factor-23 (FGF23) is a circulating factor that regulates the renal reabsorption of inorganic phosphate (Pi) and is increased in chronic kidney disease (CKD). The aim of the current investigation was to study the regulation of FGF23 in CKD subjects with various degree of renal function. As such, we analysed the relationship between FGF23, Pi, calcium, parathyriod hormone (PTH), 25(OH) vitamin D3(25(OH)D3), 1,25(OH)2 vitamin D3(1,25(OH)2D3) and estimated glomerular filtration rate (eGFR). Methods. Intact FGF23 and other biochemical variables were analysed in 72 consecutive adult out-patients with various stages of CKD (eGFR ranging from 4–96 ml/min.) Association studies were performed using linear univariate and multivariate analysis. Results. FGF23 was significantly elevated at CKD stage 4 (266 ± 315 pg/ml, P P P P P P P P Conclusions: We conclude that serum FGF23 increases in CKD 4–5, in parallel with the emerging hyperphosphataemia. Serum Pi is the most important predictor of FGF23 when GFR is less than 30 ml/min. In contrast, our data suggest that Pi may not be an important determinant of FGF23 in normophosphataemic CKD subjects. Finally, the association between FGF23 and PTH in CKD may suggest a co-regulation that remains to be further elucidated. [ABSTRACT FROM AUTHOR]