Cited by 518Parathyroid Disorders and TreatmentsBone health and osteoporosis researchAlkaline Phosphatase Research Studies

Fibroblast Growth Factor-23 Relationship to Dietary Phosphate and Renal Phosphate Handling in Healthy Young Men

Ferrari, Serge L., Bonjour, Jean-Philippe, Rizzoli, René·2005·The Journal of Clinical Endocrinology & Metabolism

Abstract

The renal handling of inorganic phosphate (Pi) is controlled not only by PTH, but also by hitherto undetermined mechanisms dependent on phosphate intake. Recently, fibroblast growth factor (FGF)-23 was identified as a novel phosphaturic factor in tumor-induced osteomalacia and autosomal-dominant hypophosphatemic rickets. We hypothesized that phosphate intake could influence FGF-23 concomitantly to the changes in renal Pi handling. Twenty-nine healthy males were subjected to a 5-d low-phosphate diet and a phosphate binder, followed by a high-phosphate diet including supplements. Concomitant modifications in calcium intake allowed minimizing PTH changes in response to dietary phosphate. Serum FGF-23 levels significantly decreased on the low-phosphate diet, then increased with the oral phosphate load. Changes in FGF-23 were positively correlated with changes in 24-h urinary Pi excretion and negatively correlated with changes in the maximal tubular reabsorption of Pi and 1,25(OH)(2)D(3) (calcitriol), whereas PTH was not. In multivariate analysis, changes in FGF-23 remained the most significantly correlated to changes in 1,25(OH)(2)D(3) and maximal tubular reabsorption of Pi. Moreover, FGF-23 was positively correlated to serum osteocalcin, a marker of osteoblastic activity. In summary, FGF-23 was inversely related to renal Pi transport and serum calcitriol levels in healthy young men. These data suggest that FGF-23 may be implicated in the physiological regulation of Pi homeostasis in response to dietary phosphate changes, independent of PTH.

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Crossref · 10.1210/jc.2004-1039

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Authors
Ferrari, S. L., Bonjour, J.-P., & Rizzoli, R.
Affiliations
  • World Health Organization (CH)
  • Service of Bone Diseases [World Health Organization Collaborating Center for Osteoporosis Prevention], Department of Rehabilitation and Geriatrics, Geneva University Hospital, Geneva 1211, Switzerland
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2005-03-01
Volume
90
Issue
3
Pages
1519-1524
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W2037498463
Cited by
518
References
35
Citations by year
2026: 5 · 2025: 8 · 2024: 12 · 2023: 13 · 2022: 19 · 2021: 31 · 2020: 22 · 2019: 23 · 2018: 27 · 2017: 21 · 2016: 27 · 2015: 21 · 2014: 27 · 2013: 34 · 2012: 45
FWCI
19.19
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Nephrology › Parathyroid Disorders and Treatments
  • Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Alkaline Phosphatase Research Studies
Keywords
fibroblast growth factor 23, dietary phosphorus, renal phosphate handling, inorganic phosphate homeostasis, parathyroid hormone, 1,25-dihydroxyvitamin D3, phosphate reabsorption, osteocalcin, phosphate binders, low phosphate diet, healthy young men
MeSH terms
Fibroblast Growth Factor-23, Adult, Calcitriol, Calcium, Dietary, Fibroblast Growth Factors, Homeostasis, Humans, Kidney, Male, Parathyroid Hormone, Phosphates, Osteocalcin, Phosphorus, Dietary

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