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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.
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.
Abstract:
Elevated C-terminal fibroblast growth factor 23 (C-FGF23) concentrations have been reported in Gambian children with and without putative Ca-deficiency rickets. The aims of this study were to investigate whether i) elevated C-FGF23 concentrations in Gambian children persist long term; ii) they are associated with higher intact FGF23 concentrations (I-FGF23), poor iron status and shorter 25-hydroxyvitamin D half-life (25OHD-t1/2); and iii) the persistence and predictors of elevated FGF23 concentrations differ between children with and without a history of rickets. Children (8-16 years, n=64) with a history of rickets and a C-FGF23 concentration >125 RU/ml (bone deformity (BD), n=20) and local community children with a previously measured elevated C-FGF23 concentration (LC+, n=20) or a previously measured C-FGF23 concentration within the normal range (LC-, n=24) participated. BD children had no remaining signs of bone deformities. C-FGF23 concentration had normalised in BD children, but remained elevated in LC+ children. All the children had I-FGF23 concentration within the normal range, but I-FGF23 concentration was higher and iron status poorer in LC+ children. 1,25-dihydroxyvitamin D was the strongest negative predictor of I-FGF23 concentration (R(2)=18%; P=0.0006) and soluble transferrin receptor was the strongest positive predictor of C-FGF23 concentration (R(2)=33%; P≤0.0001). C-FGF23 and I-FGF23 concentrations were poorly correlated with each other (R(2)=5.3%; P=0.07). 25OHD-t1/2 was shorter in BD children than in LC- children (mean (s.d.): 24.5 (6.1) and 31.5 (11.5) days respectively; P=0.05). This study demonstrated that elevated C-FGF23 concentrations normalised over time in Gambian children with a history of rickets but not in local children, suggesting a different aetiology; that children with resolved rickets had a shorter 25OHD-t1/2, suggesting a long-standing increased expenditure of 25OHD, and that iron deficiency is a predictor of elevated C-FGF23 concentrations in both groups of Gambian children.
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