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Vitamin D-binding protein in the perinatal period
European Journal of Pediatrics
|September 1, 1985
Insights
Serum vitamin D-binding protein (DBP) levels increase with fetal age and are not affected by phenotype. No DBP abnormalities were found in hypocalcemic newborns.
Area of Science:
- Biochemistry
- Neonatology
- Genetics
Background:
- Serum vitamin D-binding protein (DBP) is crucial for vitamin D transport.
- Understanding DBP levels in newborns is important for assessing calcium homeostasis.
- Gestational age and clinical conditions can potentially influence DBP levels.
Purpose of the Study:
- To investigate the molecular polymorphism and quantitative levels of serum DBP in preterm, full-term, and hypocalcemic newborn infants.
- To determine the relationship between DBP levels, phenotype, and gestational age.
- To assess if DBP abnormalities are associated with neonatal hypocalcemia.
Main Methods:
- Serum samples were collected from preterm, full-term, and hypocalcemic newborn infants.
- Molecular polymorphism of DBP was analyzed.
- Quantitative levels of serum DBP were measured.
- Statistical analysis was performed to correlate DBP levels with gestational age, phenotype, and clinical status.
Main Results:
- Serum DBP concentration increases with fetal age from 32-33 weeks to 35 weeks of gestation.
- DBP serum concentration is not influenced by DBP phenotype.
- No significant differences in DBP allele distribution or quantitative levels were observed in 29 hypocalcemic full-term newborn infants.
Conclusions:
- Serum DBP levels demonstrate a developmental trajectory during late gestation.
- DBP phenotype does not appear to affect serum DBP concentrations in newborns.
- Neonatal hypocalcemia in full-term infants is not associated with altered DBP allele distribution or quantitative levels.
Abstract:
The molecular polymorphism and quantitative levels of serum vitamin D-binding protein (DBP) were ascertained in a group of preterm, full-term and hypocalcaemic full-term newborn infants. The serum concentration of DBP is not influenced by phenotype and increases with fetal age from the 32nd-33rd week of gestation until the 35th week of gestation. Neither different DBP allele distribution nor abnormal quantitative levels found among 29 hypocalcaemic full-term newborn infants.