Abstract

ContextPhosphate homeostasis and its modifiers in early childhood are inadequately characterized.ObjectiveTo determine physiological plasma phosphate concentration and modifying factors in healthy infants at 12 to 24 months of age.DesignThis study included 525 healthy infants (53% girls), who participated in a randomized vitamin D intervention trial and received daily vitamin D3 supplementation of either 10 or 30 μg from age 2 weeks to 24 months. Biochemical parameters were measured at 12 and 24 months. Dietary phosphate intake was determined at 12 months.Main Outcome MeasuresPlasma phosphate concentrations at 12 and 24 months of age.ResultsMean (SD) phosphate concentration decreased from 12 months (1.9 ± 0.15 mmol/L) to 24 months (1.6 ± 0.17 mmol/L) of age (P < 0.001 for repeated measurements). When adjusted by covariates, such as body size, creatinine, serum 25-hydroxyvitamin D, intact and C-terminal fibroblast growth factor 23, mean plasma phosphate was higher in boys than girls during follow-up (P = 0.019). Phosphate concentrations were similar in the vitamin D intervention groups (P > 0.472 for all). Plasma iron was associated positively with plasma phosphate at both time points (B, 0.006 and 0.005; 95% CI, 0.004-0.009 and 0.002-0.008; P < 0.001 at both time points, respectively). At 24 months of age, the main modifier of phosphate concentration was plasma creatinine (B, 0.007; 95% CI 0.003-0.011, P < 0.001).ConclusionPlasma phosphate concentration decreased from age 12 to 24 months. In infants and toddlers, the strongest plasma phosphate modifiers were sex, iron, and creatinine, whereas vitamin D supplementation did not modify phosphate concentrations.

Highlights

  • Context: Phosphate homeostasis and its modifiers in early childhood are inadequately characterized

  • Phosphate homeostasis is regulated by a complex network of factors, including PTH, 1,25-dihydroxyvitamin D (1,25(OH)2D), fibroblast growth factor 23 (FGF23), and calcitonin [6,7,8]

  • As previously reported [34], intact FGF23 concentrations were higher in girls than in boys at 12 and 24 months of age (MannWhitney U test P < 0.001 for all), whereas C-terminal FGF23 concentration did not differ between the sexes (Mann-Whitney U test P > 0.499 for all) (Table 1)

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Summary

Introduction

Context: Phosphate homeostasis and its modifiers in early childhood are inadequately characterized. Objective: To determine physiological plasma phosphate concentration and modifying factors in healthy infants at 12 to 24 months of age. Main Outcome Measures: Plasma phosphate concentrations at 12 and 24 months of age. Results: Mean (SD) phosphate concentration decreased from 12 months (1.9 ± 0.15 mmol/L) to 24 months (1.6 ± 0.17 mmol/L) of age (P < 0.001 for repeated measurements). Phosphate concentrations are higher in healthy infants and children than in adults [13,14,15]. The temporal changes and factors modifying phosphate concentrations in children 12 to 24 months of age have not been previously studied. Our study examined plasma phosphate concentrations in a large cohort of healthy young Finnish children at 12 and 24 months and studied modifying factors for phosphate concentrations at these time points

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