Acute effect of oral phosphate loading on serum fibroblast growth factor 23 levels in healthy men

Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We perform...

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Published inKidney international Vol. 70; no. 12; pp. 2141 - 2147
Main Authors Nishida, Y., Taketani, Y., Yamanaka-Okumura, H., Imamura, F., Taniguchi, A., Sato, T., Shuto, E., Nashiki, K., Arai, H., Yamamoto, H., Takeda, E.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.12.2006
Nature Publishing
Elsevier Limited
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Online AccessGet full text
ISSN0085-2538
1523-1755
1523-1755
DOI10.1038/sj.ki.5002000

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Abstract Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400mg (P400), 800mg (P800), and 1200mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1h after P400 and P800 intake. Serum iPTH levels at 1–2 and 4–6h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8h after P400 intake and up to 6h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.
AbstractList Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400mg (P400), 800mg (P800), and 1200mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1h after P400 and P800 intake. Serum iPTH levels at 1–2 and 4–6h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8h after P400 intake and up to 6h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.
Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400 mg (P400), 800 mg (P800), and 1200 mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8 h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1 h after P400 and P800 intake. Serum iPTH levels at 1-2 and 4-6 h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8 h after P400 intake and up to 6 h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8 h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.
Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400 mg (P400), 800 mg (P800), and 1200 mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8 h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1 h after P400 and P800 intake. Serum iPTH levels at 1-2 and 4-6 h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8 h after P400 intake and up to 6 h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8 h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400 mg (P400), 800 mg (P800), and 1200 mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8 h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1 h after P400 and P800 intake. Serum iPTH levels at 1-2 and 4-6 h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8 h after P400 intake and up to 6 h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8 h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.
Author Taketani, Y.
Arai, H.
Imamura, F.
Sato, T.
Yamamoto, H.
Nishida, Y.
Yamanaka-Okumura, H.
Takeda, E.
Nashiki, K.
Taniguchi, A.
Shuto, E.
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  surname: Taketani
  fullname: Taketani, Y.
  email: taketani@nutr.med.tokushima-u.ac.jp
  organization: Department of Clinical Nutrition, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan
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  surname: Yamanaka-Okumura
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  fullname: Imamura, F.
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  fullname: Nashiki, K.
  organization: Department of Clinical Nutrition, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan
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  surname: Arai
  fullname: Arai, H.
  organization: Department of Clinical Nutrition, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan
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ContentType Journal Article
Copyright 2006 International Society of Nephrology
2007 INIST-CNRS
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Issue 12
Keywords parathyroid hormone
postprandial change
phosphorus metabolism
fibroblast growth factor 23
Human
Phosphates
Nephrology
Healthy subject
Fibroblast growth factor 23
Postprandial
Acute
Oral administration
Male
Phosphorus
Metabolism
Urology
Parathormone
Parathyroid hormone
Adult
Serum factor
Language English
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https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
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  article-title: Circulating concentration of FGF-23 increases as renal function declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers
  publication-title: Kidney Int
  doi: 10.1046/j.1523-1755.2003.00328.x
– volume: 98
  start-page: 6500
  year: 2001
  ident: 10.1038/sj.ki.5002000_bb0025
  article-title: Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.101545198
– volume: 89
  start-page: 3979
  year: 2004
  ident: 10.1038/sj.ki.5002000_bb0075
  article-title: Venous sampling for fibroblast growth factor-23 confirms preoperative diagnosis of tumor-induced osteomalacia
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2004-0406
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Snippet Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this...
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SubjectTerms Administration, Oral
Adult
Biological and medical sciences
Calcium - blood
Cross-Over Studies
fibroblast growth factor 23
Fibroblast Growth Factors - blood
Homeostasis - drug effects
Homeostasis - physiology
Humans
Male
Medical sciences
Nephrology. Urinary tract diseases
parathyroid hormone
Parathyroid Hormone - blood
Phosphates - administration & dosage
Phosphates - blood
Phosphates - pharmacokinetics
Phosphates - urine
phosphorus metabolism
postprandial change
Vitamin D - analogs & derivatives
Vitamin D - blood
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Title Acute effect of oral phosphate loading on serum fibroblast growth factor 23 levels in healthy men
URI https://dx.doi.org/10.1038/sj.ki.5002000
https://www.ncbi.nlm.nih.gov/pubmed/17063170
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