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Does vitamin D deficiency affect placental inflammation or infections among very low birth weight infants?
Subhash Puthuraya1,2, Sreenivas Karnati1,2, S Nadya J Kazzi2
1a Department of Pediatrics , Cleveland Clinic Children's , Cleveland , OH , USA.
Insights
Low vitamin D levels at birth in very low birth weight infants (VLBWI) were not linked to placental inflammation or neonatal infections. This study found no association between vitamin D deficiency and these adverse outcomes in VLBWI.
Area of Science:
- Neonatology
- Maternal-Fetal Medicine
- Nutritional Science
Background:
- Very low birth weight infants (VLBWI) are susceptible to infections and may have suboptimal vitamin D levels.
- Placental inflammation is a known risk factor for adverse neonatal outcomes.
- The role of 25-hydroxyvitamin D (25OH D) in protecting VLBWI from infections and inflammation requires further investigation.
Purpose of the Study:
- To investigate the association between 25-hydroxyvitamin D (25OH D) levels at birth and the presence of placental inflammation and neonatal infections in very low birth weight infants (VLBWI).
Main Methods:
- Serum 25OH D levels were measured in 89 VLBWI and 47 mothers at birth and in 78 infants at 21 days.
- Placentas were histologically examined for maternal and fetal inflammatory changes.
- Infants were categorized into deficient (≤10 ng/ml) and adequate (>10 ng/ml) 25OH D groups based on day 1 levels.
Main Results:
- Maternal and infant 25OH D levels at birth were positively correlated (p < .001).
- Infants' 25OH D levels increased significantly by day 21 (p < .001).
- No significant associations were found between deficient 25OH D levels and maternal/fetal inflammation or neonatal infections (p > .05).
Conclusions:
- Deficient 25OH D levels at birth are not associated with placental inflammation or neonatal infections in VLBWI.
- These findings suggest that vitamin D status at birth may not be a primary determinant of early inflammatory processes or infection risk in this vulnerable population.
Objective:
Examine the association between placental inflammation and neonatal infections, and 25OH vitamin D (25OH D) levels at birth among very low birth weight infants (VLBWI).
Study Design:
Serum 25OH D levels were measured in 89 VLBWI (≤1250 g) and 47 mothers on day one, and in 78 infants on day 21. Placentas were examined for maternal and fetal inflammation. Infants were divided into deficient (≤10 ng/ml) and adequate (>10 ng/ml) groups based on 25OH D levels on day 1.
Results:
Mean ± SD maternal levels of 25OH D (21 ± 9 ng/ml) correlated with infants' levels (15 ± 8 ng/ml), (p < .001). 25OH D levels were lower in deficient (32/89) than in adequate group (8 ± 2 versus 20 ± 7 ng/ml, p = .011). Infants' 25OH D levels rose significantly by day 21 (p < .001). Univariate analyses showed no differences between infant groups in maternal or fetal inflammation, or neonatal infections (p > .05). Logistic regression analyses revealed no association between deficient 25OH D levels and the odds of maternal or fetal inflammation or other infections. Levels of 25OH D did not correlate with severity of placental inflammation.
Conclusions:
Deficient levels of 25OH D at birth are not associated with the occurrence of placental inflammation or neonatal infections among VLBWI.
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