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Dynamics of the vitamin D C3-epimer levels in preterm infants
Tomas Matejek1, Bara Zapletalova1, Martin Stepan2
1Department of Paediatrics, Faculty of Medicine Hradec Kralove, Charles University in Prague, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Insights
C3-epimers, a form of vitamin D, are produced by very low birth weight infants from birth. Their levels increase throughout the first month, independent of prematurity or growth restriction.
Area of Science:
- Neonatology
- Endocrinology
- Nutritional Science
Background:
- Vitamin D is crucial for infant health, with 25-hydroxyvitamin-D [25(OH)D] being a key indicator.
- C3-epi-25(OH)D is a less common but potentially important metabolite of vitamin D.
- Understanding vitamin D metabolism in vulnerable infant populations is essential.
Purpose of the Study:
- To determine C3-epi-25(OH)D levels in very low birth weight (VLBW) infants.
- To investigate the influence of preterm birth, intrauterine growth restriction (IUGR), and season of birth on C3-epimer production.
Main Methods:
- Analysis of 25(OH)D and C3-epi-25(OH)D in maternal serum, cord blood, and infant serum at multiple time points (days 14, 28, discharge).
- Inclusion of 127 VLBW infants (birth weight <1500g).
- Statistical correlation analysis to assess relationships between vitamin D metabolites and influencing factors.
Main Results:
- C3-epi-25(OH)D levels increased significantly from birth to discharge in VLBW infants.
- C3-epimers constituted a growing proportion of total 25(OH)D, reaching over 20% by discharge.
- Neither prematurity severity nor IUGR impacted C3-epimer production; seasonal differences were noted in maternal and cord samples.
Conclusions:
- C3-epi-25(OH)D production is active in VLBW newborns, originating from fetal stores and influenced by maternal 25(OH)D.
- The C3-epimer becomes a significant component of total vitamin D metabolites within the first month of life.
- These findings highlight the functional vitamin D system in preterm infants and its developmental trajectory.
Objectives:
The primary objective was to determine levels of C3-epi-25(OH)D in very low birth weight infants. The secondary objective was to evaluate the possible influence of preterm birth, intrauterine growth restriction (IUGR), and season of birth on the production of C3-epimers.
Methods:
A total of 127 infants with birth weight less than 1,500 g met the inclusion criteria of the study. We examined 25-hydroxyvitamin-D [25(OH)D] levels and C3-epi-25(OH)D in maternal serum before labor, and in cord blood and infants' serum on days 14 and 28, and at discharge.
Results:
The mean levels (±SD) of C3-epi-25(OH)D of the cord, on day 14, on day 28, and at discharge were 2.2 (2.9), 7.7 (5.5), 11.7 (7.6) and 14.9 (11.7) nmol/L respectively. The proportion of total 25(OH)D as the C3-epimer was 6.9% (cord), 16.3% (day 14), 22.4% (day 28) and 23.3% (discharge). A statistically significant correlation between 25(OH)D and C3-epi-25(OH)D can be demonstrated from birth. The severity of immaturity and IUGR did not affect the production of C3-epimers. In summer/autumn vs. winter/spring, the mean (SD) percentage of total 25(OH)D as the C3-epimer significantly differs only in maternal serum samples and umbilical cord samples (p value <0.001).
Conclusions:
The production of C3-epi-25(OH)D is functional even in the most immature newborns, has fetal origins, and is largely dependent on circulating 25(OH)D. At the end of the first month of life, C3-epimers make up more than 20% of 25(OH)D.
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