Predictors of intact and C-terminal fibroblast growth factor 23 in Gambian children

Vickie Braithwaite1, Kerry S Jones, Shima Assar

  • 1Medical Research Council (MRC) Human Nutrition ResearchElsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK MRC KenebaKeneba, West Kiang, The Gambia.

Endocrine Connections
|November 22, 2013
PubMed

Insights

Elevated C-terminal FGF23 (C-FGF23) normalized in Gambian children with rickets history but persisted in others. Iron deficiency predicted higher C-FGF23, while resolved rickets indicated shorter 25-hydroxyvitamin D half-life.

Area of Science:

  • Pediatric endocrinology
  • Nutritional science
  • Bone metabolism

Background:

  • Elevated C-terminal fibroblast growth factor 23 (C-FGF23) has been observed in Gambian children with and without rickets.
  • Fibroblast growth factor 23 (FGF23) plays a crucial role in phosphate and vitamin D metabolism.

Purpose of the Study:

  • To investigate the long-term persistence of elevated C-FGF23 concentrations in Gambian children.
  • To determine associations between C-FGF23, intact FGF23 (I-FGF23), iron status, and 25-hydroxyvitamin D half-life (25OHD-t1/2).
  • To identify predictors of elevated FGF23 concentrations and differences between children with and without a history of rickets.

Main Methods:

  • Longitudinal study involving Gambian children (8-16 years) with a history of rickets (n=20) and community children with normal (n=24) or elevated (n=20) C-FGF23.
  • Measurements included C-FGF23, I-FGF23, iron status (soluble transferrin receptor), and 25OHD-t1/2.
  • Statistical analysis to identify predictors and correlations.

Main Results:

  • C-FGF23 normalized in children with resolved rickets but remained elevated in local community children with prior high C-FGF23.
  • Intact FGF23 (I-FGF23) was within normal ranges for all, but higher in the persistent elevated C-FGF23 group, who also had poorer iron status.
  • 1,25-dihydroxyvitamin D predicted lower I-FGF23, while soluble transferrin receptor predicted higher C-FGF23.
  • C-FGF23 and I-FGF23 showed poor correlation.
  • Children with resolved rickets had a significantly shorter 25OHD-t1/2.

Conclusions:

  • Elevated C-FGF23 normalized over time in Gambian children with a history of rickets, suggesting distinct etiologies compared to persistent elevations in the local community.
  • A shorter 25OHD-t1/2 in children with resolved rickets suggests long-term increased vitamin D expenditure.
  • Iron deficiency is a significant predictor of elevated C-FGF23 in Gambian children.

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