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Published on: August 7, 2017
Vitamin A Status in Preterm Infants Is Associated with Inflammation and Dexamethasone Exposure
Madelaine Eloranta Rossholt1,2,3, Kristina Wendel1,3, Marianne Bratlie2
1Department of Neonatal Intensive Care, Oslo University Hospital, 0450 Oslo, Norway.
Insights
Very premature infants (<29 weeks gestation) often have vitamin A deficiency, increasing bronchopulmonary dysplasia risk. Inflammation and dexamethasone treatment impact vitamin A levels, requiring careful monitoring in these vulnerable infants.
Area of Science:
- Neonatalogy
- Nutritional Biochemistry
- Pediatric Pulmonology
Background:
- Vitamin A is crucial for lung development, and deficiency is linked to bronchopulmonary dysplasia risk.
- Preterm infants, especially those <29 weeks gestation, may have altered vitamin A status.
- Inflammation and corticosteroid use are common in preterm infants and may affect nutrient levels.
Purpose of the Study:
- To investigate vitamin A status in preterm infants (<29 weeks gestation).
- To evaluate the impact of inflammation and postnatal dexamethasone exposure on blood vitamin A concentrations.
- To analyze factors associated with vitamin A deficiency in early life.
Main Methods:
- Secondary cohort analysis of the ImNuT trial (NCT03555019).
- Measurement of vitamin A (retinol) biochemistry, intake, inflammatory markers (interleukin-6), and dexamethasone exposure.
- Comparison of vitamin A levels between dexamethasone-exposed and unexposed infants.
Main Results:
- Infants exposed to dexamethasone showed significantly higher vitamin A concentrations after four weeks (1.0 vs. 0.56 µmol/L, p < 0.001).
- Pretreatment retinol levels were lower in the dexamethasone group, with 88% deficiency at one week versus 60% in the unexposed group.
- Small size for gestational age, mechanical ventilation, and elevated interleukin-6 were negatively associated with first-week retinol.
Conclusions:
- Preterm infants (<29 weeks gestation) are at high risk of vitamin A deficiency, even with recommended intakes.
- Inflammation and dexamethasone exposure significantly influence vitamin A status in preterm infants.
- Clinical interpretation of vitamin A status requires consideration of inflammatory markers and dexamethasone treatment.
Abstract:
Vitamin A has a key role in lung development and its deficiency is associated with an increased risk of bronchopulmonary dysplasia. This secondary cohort analysis of the ImNuT trial (Immature, Nutrition Therapy NCT03555019) aimed to (1) explore vitamin A status in preterm infants <29 weeks gestation and (2) assess the influence of inflammation and postnatal dexamethasone exposure on vitamin A concentrations in blood. We report detailed information on vitamin A biochemistry, vitamin A intake, markers of inflammation and dexamethasone exposure. After four weeks of age, infants exposed to dexamethasone (n = 39) showed higher vitamin A concentrations compared to unexposed infants (n = 41); median (IQR) retinol was 1.0 (0.74, 1.5) vs. 0.56 (0.41, 0.74) µmol/L, p < 0.001. Pretreatment retinol concentrations were lower in the dexamethasone group compared to non-exposed infants (p < 0.001); 88% vs. 60% of the infants were considered deficient in vitamin A (retinol < 0.7 µmol/L) at one week of age. Small size for gestational age, mechanical ventilation and elevated levels of interleukin-6 were factors negatively associated with first-week retinol concentrations. In conclusion, preterm infants <29 weeks gestation are at risk of vitamin A deficiency despite intakes that accommodate current recommendations. The presence of inflammation and dexamethasone exposure should be considered when interpreting vitamin A status.
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