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Published on: June 25, 2010
Vitamin D metabolome in preterm infants: insights into postnatal metabolism
Tomas Matejek1,2, Lukas Prchal3, Bara Zapletalova1,2
1Department of Paediatrics, Faculty of Medicine Hradec Kralove, Charles University in Prague, Hradec Kralove, Czech Republic.
Insights
Vitamin D metabolites like cholecalciferol and 25-(OH)D increase in preterm infants after birth. Their bodies may struggle to break down vitamin D in the first month of life.
Area of Science:
- Neonatal metabolism and vitamin D biochemistry.
- Endocrinology and pediatric research.
Background:
- Preterm infants often exhibit altered vitamin D metabolism.
- Understanding vitamin D metabolite dynamics is crucial for infant health.
Purpose of the Study:
- To elucidate the structure of the vitamin D metabolome in preterm infants.
- To investigate the reasons for elevated C3 epimers of 25-hydroxyvitamin D (25-(OH)D) in preterm infants' serum.
- To compare vitamin D metabolites in cord blood versus serum at 28 days of age.
Main Methods:
- Analysis of 40 preterm infants (gestational age 29+0-32+6 weeks).
- Quantification of cholecalciferol, 25-(OH)D, and C3-epimers using liquid chromatography.
- In vitro microsomal study using human liver and kidney microsomes to assess vitamin D metabolism.
Main Results:
- Cholecalciferol, 25-(OH)D, and C3-epimers were significantly lower in cord blood than in serum at 28 days.
- Metabolites indicating vitamin D degradation pathways were significantly higher in cord blood.
- Microsomal studies revealed higher levels of monohydroxylated, dihydroxylated, and mono-oxylated dihydroxylated cholecalciferol and their C3-epimers in cord blood.
Conclusions:
- Vitamin D metabolites (cholecalciferol, 25-(OH)D, C3-epimers) increase postnatally, indicating functional biosynthesis and accumulation.
- Preterm infants appear to have impaired biotransformation and degradation of vitamin D during the first month of life.
Objectives:
To describe the structure of vitamin D metabolome and investigate the possible cause of high serum levels of C3 epimers of 25-(OH)D in preterm infants, we compared the vitamin D metabolites in umbilical cord blood with serum samples taken at 28 days of age.
Methods:
We analysed 40 preterm infants (29+0-32+6 weeks of gestation). Cholecalciferol, 25-(OH)D, and its C3-epimers were measured using liquid chromatography. A microsomal study with human liver and kidney microsomes was conducted to assess vitamin D metabolism. Identified metabolites were then examined in cord blood and serum samples.
Results:
Cholecalciferol, 25-(OH)D, and its C3-epimers were significantly lower in cord blood compared to serum at 28 days of age (p<0.001 for all metabolites). Conversely, metabolites from the microsomal study (monohydroxylated-, dihydroxylated-, and mono-oxylated dihydroxylated-cholecalciferol and their C3-epimers) were significantly higher in cord blood (p<0.001 for all).
Conclusions:
Our findings indicate that cholecalciferol, 25-(OH)D, and its C3-epimers increase during the first month of life, suggesting functional biosynthesis and postnatal accumulation of these metabolites. Conversely, based on microsomal study results, it seems that biotransformation responsible for a degradation of vitamin D during the first month of life in preterm infants is functionally impaired.
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